PfbZIP85 Transcription Factor Mediates ω-3 Fatty Acid-Enriched Oil Biosynthesis by Down-Regulating PfLPAT1B Gene Expression in Plant Tissues

The basic leucine zipper (bZIP) transcription factor (TF) family is one of the biggest TF families identified so far in the plant kingdom, functioning in diverse biological processes including plant growth and development, signal transduction, and stress responses. For Perilla frutescens, a novel oilseed crop abundant in polyunsaturated fatty acids (PUFAs) (especially α-linolenic acid, ALA), the identification and biological functions of bZIP members remain limited. In this study, 101 PfbZIPs were identified in the perilla genome and classified into eleven distinct groups (Groups A, B, C, D, E, F, G, H, I, S, and UC) based on their phylogenetic relationships and gene structures. These PfbZIP genes were distributed unevenly across 18 chromosomes, with 83 pairs of them being segmental duplication genes. Moreover, 78 and 148 pairs of orthologous bZIP genes were detected between perilla and Arabidopsis or sesame, respectively. PfbZIP members belonging to the same subgroup exhibited highly conserved gene structures and functional domains, although significant differences were detected between groups. RNA-seq and RT-qPCR analysis revealed differential expressions of 101 PfbZIP genes during perilla seed development, with several PfbZIPs exhibiting significant correlations with the key oil-related genes. Y1H and GUS activity assays evidenced that PfbZIP85 downregulated the expression of the PfLPAT1B gene by physical interaction with the promoter. PfLPAT1B encodes a lysophosphatidate acyltransferase (LPAT), one of the key enzymes for triacylglycerol (TAG) assembly. Heterogeneous expression of PfbZIP85 significantly reduced the levels of TAG and UFAs (mainly C18:1 and C18:2) but enhanced C18:3 accumulation in both seeds and non-seed tissues in the transgenic tobacco lines. Furthermore, these transgenic tobacco plants showed no significantly adverse phenotype for other agronomic traits such as plant growth, thousand seed weight, and seed germination rate. Collectively, these findings offer valuable perspectives for understanding the functions of PfbZIPs in perilla, particularly in lipid metabolism, showing PfbZIP85 as a suitable target in plant genetic improvement for high-value vegetable oil production.


Introduction
Perilla frutescens (2n = 40), commonly called perilla, is one of the annual herbs belonging to the Lamiaceae family [1].There are two different varieties, namely P. frutescens var.frutescens and P. frutescens var.crisp, respectively.P. frutescens var.frutescens serves as an oilseed crop used for vegetable oil production, while P. frutescens var.crisp is utilized as an herb for its fragrant and flavorful leaves [2,3].Perilla is native to China and nowadays is extensively planted in various Asian countries such as Korea, Japan, and India [4][5][6].As decrease the accumulation of TAGs while increasing the accumulation of polar lipids, particularly digalactosyldiacylglycerol (DGDG), under nitrogen-deficient conditions [52].The overexpression of the NsbZIP1 gene generated an enhancement of neutral lipid content and a higher level of fatty acid methyl ester (FAME) compared to the wild-type Nannochloropsis salina algae CCMP1776 under nitrogen stress conditions.Furthermore, the overexpression of NsbZIP1 led to an upregulation of genes involved in lipid metabolism, including ACBP, KAS, LC-FACS, and LPAAT [53].
Collectively, bZIP TFs are found to mediate multiple life processes, including signal transduction, metabolism, growth, and development, despite different bZIP members function diversely.However, limited information is obtained for bZIP TF family members and their biological roles in perilla.Based on the known knowledge that a few bZIP TFs functioned in the regulation of lipid metabolism in some oleaginous seeds, we hypothesized that some members of PfbZIP TFs may also mediate the biosynthesis and regulation of perilla seed oils enriched with ω-3 FAs.Therefore, this study was conducted for a systematic analysis of PfbZIP TFs in perilla, aiming to elucidate their functions, particularly the PfbZIP-mediated regulation internet responsible for the biosynthesis of seed oils enriched with ω-3 FAs.The genome-wide identification of the PfbZIP genes was performed using omics-based approaches, including chromosome localization, sequence characteristics, gene structure, conserved motifs, promoter cis-acting elements, phylogenetic relationships, gene duplication, and intergenomic synteny analysis.Moreover, the expression patterns of PfbZIP genes in various tissues of perilla were extensively examined using RNA-Seq and further validated by quantitative real-time RT-PCR (RT-qPCR) in perilla seeds at various developmental stages.Finally, yeast single hybridization (Y1H) and transient co-expression assays revealed that PfbZIP85 repressed the expression of PfLPAT1B (a key gene for TAG assembly) by physical interaction with the gene promoter.Overexpression of PfbZIP85 resulted in a significant change in oil and main FA levels in both leaves and seeds of the transgenic tobacco plants, accompanied by alternations in expressions of the lipid-related genes, including the DGAT3 gene crucial for TAG assembly and other enzyme genes.This study generates a new scientific foundation for further analysis of the biological roles of PfbZIP TFs, offering valuable genetic resources for molecular breeding to enhance oil production and quality in perilla and other oil crops.

A Total of 101 PfbZIP Transcription Factors Were Identified from P. frutescens
A total of 101 PfbZIP proteins were characterized from the genome database of P. frutescens (https://www.ncbi.nlm.nih.gov/genbank;accessed on 9 March 2023) [54] by BLAST analysis.All PfbZIP TFs were renamed from PfbZIP1 to PfbZIP101.The basic physical and chemical properties of those PfbZIPs were predicted using bioinformatics, including their gene ID, physical positions of the gene on chromosomes, length of protein sequence (aa), relative molecular weight (MW), isoelectric point (pI), and grouping of all gene members (Table S2).The protein length ranged from 112 aa (PfbZIP46 and PfbZIP98) to 1269 aa (PfbZIP89), with an average of 342 aa.Their MWs ranged from 12.07 kDa (PfbZIP46) to 142.58 kDa (PfbZIP89), with an average of 37.88 kDa.The pIs of the PfbZIPs varied from 4.84 (PfbZIP14) to 10.88 (PfbZIP46), with an average of 7.10.Compared to the numbers of bZIP family members published in other plant species (Table S1), the PfbZIP family had larger members, suggesting that the PfbZIP family was extensively expanded in P. frutescens during evolution.
To ascertain the chromosomal localization of PfbZIP genes, all identified PfbZIP genes were displayed on the chromosomes of perillas using MapChart 2.32 [55].A total of 101 PfbZIP genes were distributed differentially on 18 chromosomes of perilla (Figure S1) without the PfbZIP gene on chromosomes 11 and 18.For example, chromosomes 12, 1, and 16 contained 11 and 10 PfbZIP genes, respectively, while two PfbZIPs were mapped to chromosomes 5 and 17, respectively.On the other chromosomes, the number of PfbZIP genes varied from three to eight.

Phylogenetic Analysis of PfbZIP Proteins
A phylogenetic tree was generated utilizing the neighbor-joining (N-J) method by MEGA 11.0.9 software, which included 75 AtbZIP proteins and 101 PfbZIP proteins (Figure 1).Based on the grouping of AtbZIP in Arabidopsis, PfbZIP members were divided into 11 distinct groups (Group A, B, C, D, E, F, G, H, I, and S, as well as an unclassified group UC), with 16, 4, 7, 16, 3, 3, 7, 3, 15, 18, and 9 PfbZIP proteins in each group, respectively.Furthermore, multiple sequence alignments of PfbZIP proteins with Jalview 2.11.2.7 software (Figure 2) demonstrated that most PfbZIP proteins had a basic region composed of N-x7-R/K at the N-terminal, followed by the conserved RK (or KK) and leucine zipper domains (L-x6-L-x6-L), which are typical features of bZIP proteins.Additionally, leucine (Leu) residues are substituted with valine (Val), isoleucine (Ile), or methionine (Met) in several PfbZIP proteins.
without the PfbZIP gene on chromosomes 11 and 18.For example, chromosomes 12, 1, and 16 contained 11 and 10 PfbZIP genes, respectively, while two PfbZIPs were mapped to chromosomes 5 and 17, respectively.On the other chromosomes, the number of PfbZIP genes varied from three to eight.

Phylogenetic Analysis of PfbZIP Proteins
A phylogenetic tree was generated utilizing the neighbor-joining (N-J) method by MEGA 11.0.9 software, which included 75 AtbZIP proteins and 101 PfbZIP proteins (Figure 1).Based on the grouping of AtbZIP in Arabidopsis, PfbZIP members were divided into 11 distinct groups (Group A, B, C, D, E, F, G, H, I, and S, as well as an unclassified group UC), with 16, 4, 7, 16, 3, 3, 7, 3, 15, 18, and 9 PfbZIP proteins in each group, respectively.Furthermore, multiple sequence alignments of PfbZIP proteins with Jalview 2.11.2.7 software (Figure 2) demonstrated that most PfbZIP proteins had a basic region composed of N-x7-R/K at the N-terminal, followed by the conserved RK (or KK) and leucine zipper domains (L-x6-L-x6-L), which are typical features of bZIP proteins.Additionally, leucine (Leu) residues are substituted with valine (Val), isoleucine (Ile), or methionine (Met) in several PfbZIP proteins.

Segmental Duplication and Synteny Analysis of PfbZIP Genes
It is well known that the expansion of a gene family is attributed to repetitive events occurring within the entire gene family or among certain members [12].In comparison to other reported plant species such as Arabidopsis (75 bZIPs), rice (89 bZIPs), and sesame (62 bZIPs), perilla contains more bZIP genes (101), indicating a significant expansion of the PfbZIP gene family.In order to explain the potential mechanism responsible for this expansion, we employed TBtools 2.0 software to investigate the duplication pattern of PfbZIP genes, which contain both tandem and segmental duplication.As shown in Figure 3A and Table S3, a high degree of homology was detected among PfbZIP genes across different chromosomes despite no tandem duplication.Totally, 83 pairs of segmental duplication genes were detected in the PfbZIP gene family, and the number of replicates of PfbZIP genes with segmental duplication varied from one to four.No duplication was detected for 14 PfbZIP genes, including PfbZIP7, PfbZIP11, PfbZIP13, PfbZIP14, PfbZIP27, PfbZIP29, PfbZIP38, PfbZIP41, PfbZIP49, PfbZIP55, PfbZIP72, PfbZIP76, PfbZIP81, and PfbZIP89.This result indicates that segmental duplication may serve as the core driving force in the evolution and amplification of the PfbZIP gene family.

Segmental Duplication and Synteny Analysis of PfbZIP Genes
It is well known that the expansion of a gene family is attributed to repetitive events occurring within the entire gene family or among certain members [12].In comparison to other reported plant species such as Arabidopsis (75 bZIPs), rice (89 bZIPs), and sesame (62 bZIPs), perilla contains more bZIP genes (101), indicating a significant expansion of the PfbZIP gene family.In order to explain the potential mechanism responsible for this expansion, we employed TBtools 2.0 software to investigate the duplication pattern of PfbZIP genes, which contain both tandem and segmental duplication.As shown in Figure 3A and Table S3, a high degree of homology was detected among PfbZIP genes across different chromosomes despite no tandem duplication.Totally, 83 pairs of segmental duplication genes were detected in the PfbZIP gene family, and the number of replicates of PfbZIP genes with segmental duplication varied from one to four.No duplication was detected for 14 PfbZIP genes, including PfbZIP7, PfbZIP11, PfbZIP13, PfbZIP14, PfbZIP27, PfbZIP29, PfbZIP38, PfbZIP41, PfbZIP49, PfbZIP55, PfbZIP72, PfbZIP76, PfbZIP81, and PfbZIP89.This result indicates that segmental duplication may serve as the core driving force in the evolution and amplification of the PfbZIP gene family.To deeply investigate the origin and phylogenetic evolution of PfbZIP genes, systematic comparative analysis was conducted between P. frutescens, the model plant Arabidopsis, and its closely related plant species, S. indicum.As illustrated in the comparative synteny maps (Figure 3B and Tables S4 and S5) between P. frutescens and the other two species (Arabidopsis and S. indicum), the corresponding relationships were identified between 52 PfbZIP genes and 38 AtbZIP genes, and the corresponding 78 pairs of orthologous bZIP genes were built between perilla and Arabidopsis.Remarkably, some PfbZIP genes were recognized as potential orthologs of a specific AtbZIP gene.For instance, PfbZIP8, PfbZIP15, PfbZIP65, and PfbZIP91 were found to be orthologs of AtbZIP48.Furthermore, some PfbZIP genes exhibited collinearity relationships with multiple AtbZIP genes.For example, PfbZIP65 was identified as the ortholog of AtbZIP39, AtbZIP41, and AtbZIP48 (Figure 3B and Table S4).For comparison between perilla and sesame, the corresponding relationships were also identified between 92 PfbZIP genes and 63 SibZIP genes, and then 148 pairs of orthologous bZIP genes were established between these two plant species (Figure 3B and Table S5).

Functional Classification of PfbZIP Genes by GO and KEGG
The gene ontology (GO) annotation examination indicated that 101 PfbZIP proteins were grouped into three GO terms: biological process (BP), molecular function (MF), and cellular component (CC) (Figure 4B).In biological process, PfbZIP proteins were mainly involved in 18 categories, with predominant function in response to biological regulation (GO: 0065007), followed by cellular process (GO: 0009987), metabolic process (GO: To deeply investigate the origin and phylogenetic evolution of PfbZIP genes, systematic comparative analysis was conducted between P. frutescens, the model plant Arabidopsis, and its closely related plant species, S. indicum.As illustrated in the comparative synteny maps (Figure 3B and Tables S4 and S5) between P. frutescens and the other two species (Arabidopsis and S. indicum), the corresponding relationships were identified between 52 PfbZIP genes and 38 AtbZIP genes, and the corresponding 78 pairs of orthologous bZIP genes were built between perilla and Arabidopsis.Remarkably, some PfbZIP genes were recognized as potential orthologs of a specific AtbZIP gene.For instance, PfbZIP8, PfbZIP15, PfbZIP65, and PfbZIP91 were found to be orthologs of AtbZIP48.Furthermore, some PfbZIP genes exhibited collinearity relationships with multiple AtbZIP genes.For example, PfbZIP65 was identified as the ortholog of AtbZIP39, AtbZIP41, and AtbZIP48 (Figure 3B and Table S4).For comparison between perilla and sesame, the corresponding relationships were also identified between 92 PfbZIP genes and 63 SibZIP genes, and then 148 pairs of orthologous bZIP genes were established between these two plant species (Figure 3B and Table S5).

Analysis of the Expression Patterns of the PfbZIP Genes during Perilla Seed Development
To explore the transcriptional patterns and potential roles of PfbZIP genes in perilla seed development, the expression levels (FPKM values) of PfbZIP genes were analyzed in three distinct developmental stages (10, 20, and 30 days after flowering, DAF, Figure 4A) Pathway-based analysis was performed to explore the potential roles of the PfbZIP genes.A total of 38 PfbZIP genes were distributed across three pathways in the KEGG database, including circadian rhythm-plant (ko04712), plant signal transduction (ko04075), and MAPK signaling pathway-plant (ko04016) (Figure 4C).The results illustrate that PfbZIPs may mediate the regulation of diverse life processes in perillas.

Analysis of the Expression Patterns of the PfbZIP Genes during Perilla Seed Development
To explore the transcriptional patterns and potential roles of PfbZIP genes in perilla seed development, the expression levels (FPKM values) of PfbZIP genes were analyzed in three distinct developmental stages (10, 20, and 30 days after flowering, DAF, Figure 4A) of seeds using transcriptome data obtained in our lab.As shown in the heatmap of PfbZIP gene expressions (Figure 4D), different PfbZIP genes exhibited diverse expression patterns during perilla seed development.Interestingly, a greater number of PfbZIP genes exhibited downregulation compared to those showing upregulation.Specifically, a progressively decreased pattern of expression was detected for 59 PfbZIP genes, including PfbZIP7, PfbZIP10, PfbZIP12, PfbZIP13, PfbZIP16, and so on.On the other hand, PfbZIP1, PfbZIP33, PfbZIP52, and PfbZIP95 showed an increasing trend in expression.Notably, PfbZIP3, PfbZIP18, Pf-bZIP29, PfbZIP30, PfbZIP54, and PfbZIP85 exhibited relatively high expression levels at 10 and 20 DAF, then significantly reduced at 30 DAF.Whereas, PfbZIP22, PfbZIP24, PfbZIP39, PfbZIP68, and PfbZIP99 were barely expressed during the development of perilla seeds.
To further investigate the function of PfbZIP genes, RT-qPCR analysis was employed to assess the expression patterns of PfbZIP genes in developing perilla seeds.The expression abundances of the eight selected PfbZIP genes were analyzed in the developmental seeds of 'Jinzisu 1' (Figure 4E).These eight PfbZIP genes exhibited differential expression patterns across various developmental stages of seeds.In accordance with the transcriptome data, the relative expression levels of the PfbZIP4, PfbZIP5, PfbZIP9, and PfbZIP91 genes exhibited an initial fast increase and then a subsequent decrease during seed development.The levels of PfbZIP48 and PfbZIP71 gene expressions exhibited a gradual reduction during seed development.In contrast, the expression levels of the PfbZIP1 and PfbZIP33 genes gradually increased.Notably, the expression abundance of the PfbZIP33 gene was found to be much higher than that of other PfbZIP members.These findings suggest that most PfbZIP genes possess constitutive functionality in perilla seed development, with a number of them acting differentially across distinct seed developmental stages.

Identification of Candidate PfbZIP TFs Mediating Transcription and Regulation of Enzyme Genes Involved in Lipid Metabolism
The bZIP TF can selectively bind to the A/C/T/CACGTG/C/T/A or GCCACGTGGA motif sequences, thereby activating or inhibiting expression of the target genes [22,25].To ascertain whether PfbZIP TFs regulate transcription of lipid-associated genes, cis-elements in the promoter sequences of lipid synthesis-related genes in perilla were examined through the Plantcare website to detect the bZIP-binding cis-elements in these selected genes.As shown in Table 1, the bZIP-binding motif sequences (ACGT) were identified in the promoter regions of eight genes associated with lipid metabolism.These eight lipid-related genes contained three de novo FA synthesis enzymes (PfKAS2, PfSAD2, and PfFAD6) three FA desaturases, and five acyltransferases (PfGPAT1, PfLPAT1B, PfDGAT2A, PfDGAT3A, and PfPDAT2B).This cis-element analysis indicates that these eight lipid-related genes may be regulated by PfbZIP TFs.Dynamic analysis was conducted for total lipid accumulation during perilla seed development.As shown in Figure 5A, total lipid content was just 5.79 µg/mg at 10 DAF and then started a slow increase to 36.88 µg/mg at 20 DAF and sharply enriched to 192.45 µg/mg at 30 DAF, followed by the peak level of 360.15 µg/mg at 40 DAF (the seed almost matured).In accordance with this dynamic of total lipid accumulation (Figure 5A), the expression levels of PfbZIP1/33/42/50/52/85/88/95 (Figure 4D) were significantly upregulated throughout the fast accumulation stage of total lipid in perilla seeds, indicating that these eight PfbZIPs may function importantly for the lipid/FA biosynthesis pathway in perilla seeds.
Int. J. Mol.Sci.2024, 25, x FOR PEER REVIEW 9 of 25 then started a slow increase to 36.88 µg/mg at 20 DAF and sharply enriched to 192.45 µg/mg at 30 DAF, followed by the peak level of 360.15 µg/mg at 40 DAF (the seed almost matured).In accordance with this dynamic of total lipid accumulation (Figure 5A), the expression levels of PfbZIP1/33/42/50/52/85/88/95 (Figure 4D) were significantly upregulated throughout the fast accumulation stage of total lipid in perilla seeds, indicating that these eight PfbZIPs may function importantly for the lipid/FA biosynthesis pathway in perilla seeds.Therefore, we further investigated the expression correlation between these eight PfbZIP TFs and the aforementioned eight key lipid-related enzyme genes.As shown in Figure 5B, the expressions of both PfbZIP52 and PfbZIP33 exhibited a significantly positive correlation (p < 0.001) with the expressions of the PfPDAT2B and PfGPAT1 genes.However, the expression of PfbZIP33 displayed a strong negative correlation (p < 0.001) with the expression of the PfFAD6 gene.Remarkably, PfbZIP85 displayed an extremely negative association (p < 0.001) with PfLPAT1B.Such expression correlation analysis demonstrates that PfPDAT2B and PfGPAT1 genes may be the downstream targets of PfbZIP52 Therefore, we further investigated the expression correlation between these eight PfbZIP TFs and the aforementioned eight key lipid-related enzyme genes.As shown in Figure 5B, the expressions of both PfbZIP52 and PfbZIP33 exhibited a significantly positive correlation (p < 0.001) with the expressions of the PfPDAT2B and PfGPAT1 genes.However, the expression of PfbZIP33 displayed a strong negative correlation (p < 0.001) with the expression of the PfFAD6 gene.Remarkably, PfbZIP85 displayed an extremely negative association (p < 0.001) with PfLPAT1B.Such expression correlation analysis demonstrates that PfPDAT2B and PfGPAT1 genes may be the downstream targets of PfbZIP52 and PfbZIP33 TFs, while the PfLPAT1B gene may be the target of PfbZIP85.Moreover, this suggests that these three PfbZIP TFs might be the candidate bZIP TFs directly regulating the transcription levels of the lipid genes in perilla, thereby mediating FA/oil biosynthesis and accumulation.

PfbZIP85 Rather than PfbZIP52 Physically Interacts with Promoters of the Downstream Target Genes Revealed by the Yeast One-Hybrid Assay
To verify whether the candidate PfbZIPs directly regulate the downstream target genes, a yeast one-hybrid (Y1H) assay was employed to investigate the physical interaction between PfbZIP52/85 and the promoters of the PfGPAT1/PfLPAT1B genes, respectively.The CDS of PfbZIP52 and PfbZIP85 genes were isolated from the perilla variety 'Jinzisu 1' (Figure S2) and then separately inserted into the prey vector pGADT7 to form pGADT7-PfbZIP52 and pGADT7-PfbZIP85, respectively (Figure S3).At the same time, the ACGT element-containing promoter sequences of PfGPAT1 and PfLPAT1B genes were isolated and separately inserted into the bait vector pHIS2 to generate pHIS2-proPfGPAT1 and pHIS2-proPfLPAT1B, respectively (Figure S3).
Therefore, SD-TLH medium supplemented with 30 mmol/L 3AT was used in Y1H to further investigate the interaction between PfbZIP52 and the PfGPAT1 promoter, as well as PfbZIP85 and the PfLPAT1B promoter, respectively.As shown in Figure 5C, the positive control pHIS2-P53 + pGAD53m exhibited normal growth on all the tested media, including SD-TL, SD-TLH, and SD-TLH + 30 mmol/L 3AT.However, the growth of the control groups, pHIS2-proPfGPAT1 + pGADT7 and pHIS2-proPfLPAT1B + pGADT7, was inhibited on SD-TLH + 30 mmol/L 3AT medium.Remarkably, the yeast strains co-expressed with pHIS2-proPfLPAT1B + pGADT7-PfbZIP85 grew normally on the medium of SD-TLH + 30 mmol/L 3AT, while the yeast co-expressed with pHIS2-proPfGPAT1 + pGADT7-PfbZIP52 failed to grow.Taken together, no interaction was observed between the PfGPAT1 promoter and PfbZIP52 TF.Notably, PfbZIP85 TF can physically interact with the promoter of the PfLPAT1B gene, suggesting that PfbZIP85 TF may directly modulate the expression of the downstream target gene PfLPAT1B, one of the key genes for TAG assembly.

PfbZIP85 Is Localized in the Nucleus and Negatively Regulates the Expression of the PfLPAT1B Gene
To further characterize the PfbZIP85 TF, we constructed a recombinant fusion plasmid (35S::PfbZIP85::GFP) (Figure S3) and analyzed the subcellular localization of the PfbZIP85 protein.This vector containing PfbZIP85 fused with GFP was transiently expressed in N. benthamiana leaves, while the empty vector pCAMBIA1300/GFP was used as the negative control.As observed in Figure 6A, the green fluorescence signal from the 35S::GFP fusion vector was exhibited in both the nucleus and cytoplasm membrane, while the 35S::PfbZIP85::GFP fusion vector generated a green fluorescence signal only in the nucleus of the cell, confirming that PfbZIP85 TF is a nuclear-localized protein.
Subsequently, a GUS assay was used to identify the regulatory mechanism of PfbZIP85 TF on the PfLPAT1B gene.The promoter (2000 bp in length) of the PfLPAT1B gene (Figure S5) was fused with the GUS report gene of the pCAMBIA1301 vector to form a fusion expression vector of proPfLPAT1B (proPfLPAT1B::GUS) (Figure S3).The proPfLPAT1B::GUS plasmid alone or with 35S::PfbZIP85 was transiently expressed in tobacco leaves.The tobacco plants cultured for 36 h to 48 h were taken for GUS staining detection.As observed in Figure 6B, the leaves co-infiltrated with 35S::PfbZIP85 and proPfLPAT1B::GUS displayed a lighter blue color (GUS activity) than those infiltrated with proPfLPAT1B::GUS alone.Further RT-qPCR examination of the relative expression level of the GUS gene in tobacco leaf samples revealed that the GUS expression in the leaves co-infiltrated with 35S::PfbZIP85 and proPfLPAT1B::GUS was significantly reduced by 70.12% (p < 0.05) compared to the leaves infiltrated with proPfLPAT1B::GUS alone (Figure 6C).Collectively, these results demonstrate that PfbZIP85 exerts a negative regulatory role on the expression of the PfLPAT1B gene.
a fusion expression vector of proPfLPAT1B (proPfLPAT1B::GUS) (Figure S3).The proPfLPAT1B::GUS plasmid alone or with 35S::PfbZIP85 was transiently expressed in tobacco leaves.The tobacco plants cultured for 36 h to 48 h were taken for GUS staining detection.As observed in Figure 6B, the leaves co-infiltrated with 35S::PfbZIP85 and proPfLPAT1B::GUS displayed a lighter blue color (GUS activity) than those infiltrated with proPfLPAT1B::GUS alone.Further RT-qPCR examination of the relative expression level of the GUS gene in tobacco leaf samples revealed that the GUS expression in the leaves co-infiltrated with 35S::PfbZIP85 and proPfLPAT1B::GUS was significantly reduced by 70.12% (p < 0.05) compared to the leaves infiltrated with proPfLPAT1B::GUS alone (Figure 6C).Collectively, these results demonstrate that PfbZIP85 exerts a negative regulatory role on the expression of the PfLPAT1B gene.

Heterogeneous Expression of PfbZIP85 Resulted in a Reduction of TAG Content and an Alternation of TAG-Associated FAs in Transgenic Tobacco Lines
To further evaluate the functions of PfbZIP85 and its potential as a target in biological engineering to enhance the production and quality of vegetable oils/TAG, plant constitutive expression vectors and seed-specific expression vectors of the PfbZIP85 gene were constructed (Figure S3) and subsequently transformed into common tobacco, respectively.The wild-type (WT) tobacco plants were employed as the negative controls.The PfbZIP85expressed plants were identified (Figure S6), and then three independent transgenic lines exhibiting higher expression of PfbZIP85 were used as the samples for phenotypic assessment, including TAG content, FA profiles, as well as other agronomic characteristics.
Total lipid was extracted from leaves (Figure 7A) or seeds (Figure 7D) from tobacco plants overexpressing PfbZIP85, followed by the preparation of FAMEs for measuring the contents of total oil and TAG-associated FAs through GC (see the Section 4 for details).As displayed in Figure 7B, the TAG content in the leaves was significantly decreased from 0.84 µg/mg in the WT lines to 0.51 µg/mg in PfbZIP85-expressing lines (p < 0.05).Additionally, the TAG-associated FA profiles were identical between WT and PfbZIP85-expressing tobacco leaves (Figure 7C).PfbZIP85-expressing lines indicated a significant increase in the levels of C18:3 and C16:0 by 2.54% and 4.25% (p < 0.05), respectively, compared to the WT lines in leaf tissues.Correspondingly, the levels of C18:1 and C18:2 were both notably decreased by 3.78% and 3.42% (p < 0.05) in the PfbZIP85-expressing tobacco leaves, and the C20:0 exhibited a small reduction compared to the WT lines (Figure 7C).Similarly, the TAG content in the seeds was significantly decreased from 31.74 µg/seed in the WT lines to 27.25 µg/seed in PfbZIP85-expressing lines (p < 0.05) (Figure 7E).FA profiles in TAGs from tobacco seeds (Figure 7F) also indicated the same alteration trend as the case in leaves, with contents of C18:3 and C16:0 notably enhanced by 3.42% and 2.50% (p < 0.05), respectively, followed by a remarkable reduction of C18:1 and C18:2 contents (p < 0.05) in transgenic tobacco seeds compared to the WT seeds (Figure 7F).These results indicate that PfbZIP85 can function efficiently in the ectopic host, affecting the TAG level and ratio of major TAG-associated FAs in plant seeds or non-seed tissues.
To further evaluate the functions of PfbZIP85 and its potential as a target in biological engineering to enhance the production and quality of vegetable oils/TAG, plant constitutive expression vectors and seed-specific expression vectors of the PfbZIP85 gene were constructed (Figure S3) and subsequently transformed into common tobacco, respectively.The wild-type (WT) tobacco plants were employed as the negative controls.The PfbZIP85expressed plants were identified (Figure S6), and then three independent transgenic lines exhibiting higher expression of PfbZIP85 were used as the samples for phenotypic assessment, including TAG content, FA profiles, as well as other agronomic characteristics.
Total lipid was extracted from leaves (Figure 7A) or seeds (Figure 7D) from tobacco plants overexpressing PfbZIP85, followed by the preparation of FAMEs for measuring the contents of total oil and TAG-associated FAs through GC (see the Section 4 for details).As displayed in Figure 7B, the TAG content in the leaves was significantly decreased from 0.84 µg/mg in the WT lines to 0.51 µg/mg in PfbZIP85-expressing lines (p < 0.05).Additionally, the TAG-associated FA profiles were identical between the WT and PfbZIP85expressing tobacco leaves (Figure 7C).PfbZIP85-expressing lines indicated a significant increase in the levels of C18:3 and C16:0 by 2.54% and 4.25% (p < 0.05), respectively, compared to the WT lines in leaf tissues.Correspondingly, the levels of C18:1 and C18:2 were both notably decreased by 3.78% and 3.42% (p < 0.05) in the PfbZIP85-expressing tobacco leaves, and the C20:0 exhibited a small reduction compared to the WT lines (Figure 7C).Similarly, the TAG content in the seeds was significantly decreased from 31.74 µg/seed in the WT lines to 27.25 µg/seed in PfbZIP85-expressing lines (p < 0.05) (Figure 7E).FA profiles in TAGs from tobacco seeds (Figure 7F) also indicated the same alteration trend as the case in leaves, with contents of C18:3 and C16:0 notably enhanced by 3.42% and 2.50% (p < 0.05), respectively, followed by a remarkable reduction of C18:1 and C18:2 contents (p < 0.05) in transgenic tobacco seeds compared to the WT seeds (Figure 7F).These results indicate that PfbZIP85 can function efficiently in the ectopic host, affecting the TAG level and ratio of major TAG-associated FAs in plant seeds or non-seed tissues.

Overexpression of PfbZIP85 Results in No Significantly Negative Impacts on Other Agronomic Traits of Tobacco Plants
To examine whether the overexpression of PfbZIP85 affects other physiological characteristics in the heterogeneous host, we measured the contents of starch, soluble sugar, and protein, leaf photosynthesis (Pn), leaf dry weight (LDW), thousand seed weight (TSW), and seed germination rate.As illustrated in Figure 8A, the starch content in seeds was significantly decreased from 3.20% in the WT to 1.88% in PfbZIP85-expressing lines (p < 0.05).Whereas, soluble sugar content exhibited a significant enhancement of 3.89% (p < 0.05) in the PfbZIP85-expressing lines compared to WT lines (Figure 8B).Protein content in tobacco leaves displayed no obvious difference between the WT lines and the transgenic plants (Figure 8C).In addition, no apparent distinctions were examined for leaf Pn (Figure 8D), LDW (Figure 8E), or germination rate (Figure 8F) among all the tested samples.In short, these findings illustrate that the expression of PfbZIP85 in tobacco can notably reduce TAG, C18:1, and C18:2 levels but increase C18:3 content without a significant penalty on other agronomy traits despite the increased starch level.Speculatively, down-regulation of PfbZIP85 might increase TAG accumulation and C18:1 and C18:2 contents in perilla seeds.gene.The TAG contents are expressed by the mass of esterified fatty acids.Values are presented as mean ± SD (n = 3).Different lowercase letters indicate significant differences at p < 0.05.

Overexpression of PfbZIP85 Results in No Significantly Negative Impacts on Other Agronomic Traits of Tobacco Plants
To examine whether the overexpression of PfbZIP85 affects other physiological characteristics in the heterogeneous host, we measured the contents of starch, soluble sugar, and protein, leaf photosynthesis (Pn), leaf dry weight (LDW), thousand seed weight (TSW), and seed germination rate.As illustrated in Figure 8A, the starch content in seeds was significantly decreased from 3.20% in the WT lines to 1.88% in PfbZIP85-expressing lines (p < 0.05).Whereas, soluble sugar content exhibited a significant enhancement of 3.89% (p < 0.05) in the PfbZIP85-expressing lines compared to WT lines (Figure 8B).Protein content in tobacco leaves displayed no obvious difference between the WT lines and the transgenic plants (Figure 8C).In addition, no apparent distinctions were examined for leaf Pn (Figure 8D), LDW (Figure 8E), or germination rate (Figure 8F) among all the tested samples.In short, these findings illustrate that the expression of PfbZIP85 in tobacco can notably reduce TAG, C18:1, and C18:2 levels but increase C18:3 content without a significant penalty on other agronomy traits despite the increased starch level.Speculatively, down-regulation of PfbZIP85 might increase TAG accumulation and C18:1 and C18:2 contents in perilla seeds.

Overexpression of PfbZIP85 Affects the Expression of Genes Associated with Lipid Metabolism in Tobacco Plants
To further investigate the potential molecular mechanism of PfbZIP85 in heterogeneous host tobacco plants, we examined the expression patterns of the twelve lipid genes in the transgenic tobacco plants overexpressing PfbZIP85.The tested twelve genes included the genes encoding ∆ 9 stearoyl-ACP desaturase (SAD1), fatty acid desaturases (FAD2 and FAD3), glycerol-3-phosphate acyltransferase (GPAT9), lysophosphatidic acid acyltransferases (LPAT1 and LPAT2), phosphatidylcholine diacylglycerol choline phosphotransferase (PDCT), phospholipid diacylglycerol acyltransferase (PDAT), lysophosphatidylcholine acyltransferase (LPCAT), and diacylglycerol acyltransferases (DGAT1, DGAT2, and DGAT3), respectively.As shown in Figure 9, the expression levels of NtSAD1, NtFAD2, NtFAD3, Nt-GPAT9, NtLPAT1, NtLPAT2, NtPDCT, NtPDAT, NtLPCAT, NtDGAT1, and NtDGAT2 genes were significantly decreased in PfbZIP85-expressing tobacco plants compared with WT plants.Remarkably, the expression level of NtDGAT3 was significantly increased, exhibit-ing a 40.32-fold enhancement compared to the WT plants (Figure 9).The down-regulation of these endogenous genes responsible for FA/oil biosynthesis might contribute to the decrease in TAG accumulation in the transgenic tobacco tissues.Moreover, PfbZIP85 can negatively regulate NtLPAT1/2 expressions and possibly down-regulate the expressions of other lipid-related genes (NtSAD1, NtFAD2, NtFAD3, and so on), except for increasing NtDGAT3 expression.Collectively, these findings demonstrate that the PfbZIP85 protein has the potential to modulate FA/oil biosynthesis and accumulation by regulating the expressions of lipid biosynthesis-related genes.
Int. J. Mol.Sci.2024, 25, x FOR PEER REVIEW 14 of 25 DGAT3), respectively.As shown in Figure 9, the expression levels of NtSAD1, NtFAD2, NtFAD3, NtGPAT9, NtLPAT1, NtLPAT2, NtPDCT, NtPDAT, NtLPCAT, NtDGAT1, and NtDGAT2 genes were significantly decreased in PfbZIP85-expressing tobacco plants compared with WT plants.Remarkably, the expression level of NtDGAT3 was significantly increased, exhibiting a 40.32-fold enhancement compared to the WT plants (Figure 9).The down-regulation of these endogenous genes responsible for FA/oil biosynthesis might contribute to the decrease in TAG accumulation in the transgenic tobacco tissues.Moreover, PfbZIP85 can negatively regulate NtLPAT1/2 expressions and possibly down-regulate the expressions of other lipid-related genes (NtSAD1, NtFAD2, NtFAD3, and so on), except for increasing NtDGAT3 expression.Collectively, these findings demonstrate that the PfbZIP85 protein has the potential to modulate FA/oil biosynthesis and accumulation by regulating the expressions of lipid biosynthesis-related genes.

Discussion
Perilla frutescens is a specific oilseed crop because of its nutritional and medicinal properties, with its seed containing 46-58% oil [56].Perilla seed oil is rich in UFAs (more than 90%), with a high level of α-linolenic acid (>65%) [2].Therefore, an in-depth analysis of the biosynthesis and regulatory mechanisms of ALA-enriched oil in perilla seed would provide valuable insights for improving the oil yield and quality of perilla seed and other oilseeds, thereby meeting the growing market demand for nutrient-healthy vegetable oils.A number of TFs were identified to mediate regulation of multiple life processes, including FA/oil biosynthesis in plants [49][50][51][52][53].Of them, bZIP TFs were found to play a key

Discussion
Perilla frutescens is a specific oilseed crop because of its nutritional and medicinal properties, with its seed containing 46-58% oil [56].Perilla seed oil is rich in UFAs (more than 90%), with a high level of α-linolenic acid (>65%) [2].Therefore, an in-depth analysis of the biosynthesis and regulatory mechanisms of ALA-enriched oil in perilla seed would provide valuable insights for improving the oil yield and quality of perilla seed and other oilseeds, thereby meeting the growing market demand for nutrient-healthy vegetable oils.A number of TFs were identified to mediate regulation of multiple life processes, including FA/oil biosynthesis in plants [49][50][51][52][53].Of them, bZIP TFs were found to play a key regulatory role in various plants [30,[57][58][59].However, perilla PfbZIP members and their functions remain unknown yet.In the present study, a genome-wide identification of perilla PfbZIP was performed, followed by functional characterization of PfbZIP85 through yeast one-hybrid (Y1H) assays and tobacco genetic transformations, aiming to enhance our comprehension of PfbZIP roles in FA/oil metabolism and also providing valuable bZIP TFs as targets for plant lipid metabolic engineering.
All these 101 PfbZIP proteins were divided into 11 groups (groups A, B, C, D, E, F, G, H, I, S, and UC) (Figure 1).Especially, nine PfbZIP proteins (PfbZIP14, 19, 22, 24, 38, 41, 49, 68, and 76) were classified into the UC group, suggesting they might be new members generated during the evolution of the PfbZIP family.Multiple protein sequence alignment analyses disclosed that except for the PfbZIP members within the UC group, all other PfbZIP proteins contained a highly conserved basic region (N-x7-R/K) at the N-terminus, which is essential for DNA binding and nuclear localization (Figure 2) [33].Moreover, the C-terminus of these PfbZIP proteins had a highly conserved leucine zipper region (L-x6-L-x6-L), which is related to specific recognition and dimerization of PfbZIP proteins (Figure 2) [26,27].Additionally, the same conserved motifs and a high degree of sequence similarity among PfbZIP members in the same group suggest potential functional redundancy.
Gene duplication played a crucial role in gene family expansion and genome evolution [49,60].In our study, 83 pairs of segmental duplicated PfbZIP genes were observed, accounting for approximately 82.2% of the PfbZIPs.Meanwhile, no tandem duplications were discovered among the PfbZIP genes (Figure 3A).Therefore, segmental duplication plays a predominant role in the expansion and evolution of the PfbZIP gene members in perilla, which is consistent with previous findings in rice [27], sesame [33], and grapevine [61].Previous studies have demonstrated that gene duplication leads to the divergence of spatiotemporal expression patterns of genes [62][63][64].Thus, we further analyzed the expression profiles of all PfbZIP members in the developing seeds of perilla.The results showed that these 83 pairs of PfbZIP genes exhibited various expression patterns (Figure 4D) across different developmental stages of perilla seeds, indicating that functional divergence occurred in these gene pairs during evolution.The difference in expression levels among PfbZIP members might be the fundamental cause of their functional differences.In addition, 101 PfbZIP genes were enriched in three GO functional categories: BP, MF, and CC (Figure 4B) by GO analysis, and 38 of the 101 PfbZIP genes were enriched in three pathways (e.g., plant signal transduction, circadian rhythm-plant, and MAPK signaling pathway-plant) (Figure 4C) by KEGG analysis.Both GO and KEGG analyses indicate that PfbZIPs may mediate signal transduction processes in perilla plants (e.g., abscisic acid (ABA) and jasmonic acid (JA) signal transduction pathways).

PfbZIP Members May Play Significant Roles in Lipid Biosynthesis by Regulating the Expression of Lipid-Associated Genes
Transcription factors regulate the transcriptional level of other transcription factors or their downstream target genes via binding with DNA cis-acting elements [22,25].Despite a number of bZIP TFs being identified in various plants and their diverse functions being reported [36,48,65], only a few bZIP members were detected to mediate lipid metabolism.To identify whether PfbZIP members regulate FA/oil metabolism in perilla seeds, expression profiles of PfbZIP genes were examined during perilla seed development by RNA-Seq and RT-qPCR.As shown in Figure 4D,E, different PfbZIP members exhibited distinct expression patterns at different developmental stages of perilla seeds, suggesting that different PfbZIP members may function diversely during seed development.Furthermore, the expression abundances of the eight PfbZIP members (PfbZIP1/33/42/50/52/85/88/95) were obviously upregulated in the rapid oil-enrichment period in perilla seeds (Figures 4D and 5A), indicating that these PfbZIP members may function crucially in the regulation of FA/oil accumulation in perilla seeds.
Interestingly, one or more bZIP-binding cis-elements (ACGT) were present in the promoters of the eight key FA/oil-related enzyme genes (PfKAS2, PfSAD2, PfFAD6, PfGPAT1, PfLPAT1B, PfDGAT2A, PfDGAT3A, and PfPDAT2B) (Table 1), demonstrating that these eight enzyme genes may be regulated by PfbZIP TFs.Subsequently, the expression correlation analysis indicated that the expression of some PfbZIP genes was significantly correlated with the oil-related enzyme genes (Figure 5B).For instance, a highly significant positive correlation was observed between the expression of PfbZIP52 and PfGPAT1, whereas a highly remarkable negative correlation was detected between the expression of PfbZIP85 and PfLPAT1B (Figure 5B).These data further indicate that PfbZIP might mediate FA/oil biosynthesis by regulating the expressions of the lipid genes in perilla developmental seeds.Finally, the Y1H test and GUS activity assay evidenced that PfbZIP85 TF negatively regulated PfLPAT1B's expression by physical interaction with the promoter of the PfLPAT1B gene (Figures 5C and 6B,C).In accordance with the regulatory function of PfbZIP85 identified here, AtbZIP67 in Arabidopsis [50] and RcbZIP in castor bean [25] were reported to bind to the ACGT elements and then modulate the transcriptional activity of their respective downstream target genes.

PfbZIP85 Can Be Used as a Genetic Modification Target to Enhance Oil Production and Quality in Plant Seed or Non-Seed Tissues
The bZIP TF family is one of the important families in the plant kingdom [66,67], mainly participating in the modulation of plant growth and development, organ differentiation [36][37][38], energy metabolism homeostasis [39][40][41], transcriptional control of genes associated with seed storage substances [42], abiotic stress response [43][44][45][46][47][48], as well as FA/oil biosynthesis and accumulation [49][50][51][52][53].For example, AtbZIP67 specifically binds to the G-box element within the AtFAD3 promoter region and improves the biosynthesis of C18:3 in transgenic Arabidopsis seeds [50].Overexpression of the GmbZIP123 gene in Arabidopsis improved oil content in transgenic plant seeds [51].Furthermore, overexpression of NsbZIP1 from N. salina algae CCMP1776 leads to an upregulation of the transcription of lipid genes including ACBP, KAS, LC-FACS, and LPAAT in algal cells under nitrogen stress, along with a significant improvement of neutral lipid contents [53].However, bZIP TFs can also inhibit plant lipid synthesis and accumulation.For instance, overexpression of AtbZIP52 resulted in a decrease in seed oil level in the transgenic plant lines, whereas an enhancement of seed oil accumulation was observed in the Atbzip52 loss-of-function mutant lines compared with WT Arabidopsis [67].
In this study, common tobacco was used as the heterogeneous host to overexpress the PfbZIP85 gene to assess the potential of PfbZIP85 in genetic engineering for regulating TAG accumulation and FA profiles in both leaves and seeds.Our findings exhibited a significant reduction of TAG content in the transgenic tobacco leaves (Figure 7B).Similarly, a reduction was observed for TAG content in the transgenic tobacco seeds (Figure 7E).Moreover, the ratio of FA compositions in TAGs was also changed within PfbZIP85-transgenic tobacco leaves and seeds, showing significant increases in C18:3 and C16:0 contents, accompanied by remarkable decreases in the levels of C18:1 and C18:2 (Figure 7C,F).For the analysis of TAG-associated FAs, the accuracy may be improved by using other non-destructive reagents (2,7-dichlorofluorescein, rhodamine, or primulin) for displaying silica gel zones on TLC containing lipids, instead of iodine vapor (an oxidizing agent), which may damage lipids, particularly polyunsaturated fatty acids.
In contrast to the reduction of both total oil and starch contents (Figures 7B and 8A), overexpression of PfbZIP85 led to an increase in soluble sugar content (Figure 8B), while the protein content (Figure 8C) remained unchanged.These findings suggest that PfbZIP85 inhibits carbon flux into the FA/oil pathway but increases carbon flux to store soluble sugar in the tissue.Interestingly, no negative effect was observed on other agronomic traits, including leaf Pn, leaf dry weight, and germination rate (Figure 8D-F), in the transgenic tobacco lines.Further gene expression analysis uncovered that overexpression of PfbZIP85 resulted in an expression change of the 12 lipid biosynthesis enzyme genes in the transgenic tobacco lines (Figure 9), showing a reduced expression of the 11 endogenous enzyme genes but an increased expression of the NtDGAT3 gene compared to the WT controls.Taken together, PfbZIP85 from perilla can be recognized as a target in lipid metabolic engineering to regulate oil yield and target FA enrichment in the heterogeneous plant host, despite the detailed regulation mechanism of FA/oil biosynthesis and accumulation mediated by PfbZIP85 or its homolog in different plants needing further investigation.Based on these findings, therefore, we proposed a possible regulatory mechanism for FA/oil metabolism mediated by PfbZIP85 TF in plant tissues (Figure 10).
In contrast to the reduction of both total oil and starch contents (Figures 7B an overexpression of PfbZIP85 led to an increase in soluble sugar content (Figure 8B), the protein content (Figure 8C) remained unchanged.These findings sugges PfbZIP85 inhibits carbon flux into the FA/oil pathway but increases carbon flux to soluble sugar in the tissue.Interestingly, no negative effect was observed on other nomic traits, including leaf Pn, leaf dry weight, and germination rate (Figure 8DF), transgenic tobacco lines.Further gene expression analysis uncovered that overexpre of PfbZIP85 resulted in an expression change of the 12 lipid biosynthesis enzyme ge the transgenic tobacco lines (Figure 9), showing a reduced expression of the 11 en nous enzyme genes but an increased expression of the NtDGAT3 gene compared WT controls.Taken together, PfbZIP85 from perilla can be recognized as a target in metabolic engineering to regulate oil yield and target FA enrichment in the heteroge plant host, despite the detailed regulation mechanism of FA/oil biosynthesis and acc lation mediated by PfbZIP85 or its homolog in different plants needing further inve tion.Based on these findings, therefore, we proposed a possible regulatory mechanis FA/oil metabolism mediated by PfbZIP85 TF in plant tissues (Figure 10).Recently, AtbZIP52 was found to interact with AtWRI1, a core transcriptional re tor in the lipid biosynthesis pathway, leading to the down-regulation of several fatt biosynthesis genes and thus reduced oil production in Arabidopsis seeds [67] croRNA167 was identified to target the CsARF8 transcription factor in Camelina sativ CsARF8 upregulated the expression of the CsFAD3 gene by cooperating with bZIP6 ABI3, thereby affecting ALA biosynthesis in C. sativa seeds [68].Increasing data ind that plant seed oil biosynthesis and accumulation were controlled by a complex and m level regulatory mechanism, particularly a network of interacting transcriptional a tors and repressors [69].Our study identified PfbZIP85 as a negative regulator in p seed oil biosynthesis, showing that PfbZIP85 can be a target in genetic engineering f improvement of oil yield and quality in heterogenous hosts.Further research nee address whether other TFs or miRNAs and even epigenetic regulators interact PfbZIP85 and to identify more target genes of PfbZIP85, which will deepen our u standing of the PfbZIP85-mediated internet responsible for FA/oil biosynthesis d seed development and other biological processes.

Biological Materials
The high-oil-content perilla (Perilla frutescens) variety 'Jinzisu 1' was selected fo study and grown in Taigu District, Shanxi Province, China (112°58′ E, 37°42′ N).See 'Jinzisu 1' were harvested at 10, 20, and 30 days after flowering (DAF).All samples promptly flash-frozen using liquid nitrogen and subsequently stored at −80 °C for fu experiments.The tobacco species Nicotiana benthamiana was employed for protein su lular localization in this study, while the common tobacco species Nicotiana tabacum Recently, AtbZIP52 was found to interact with AtWRI1, a core transcriptional regulator in the lipid biosynthesis pathway, leading to the down-regulation of several fatty acid biosynthesis genes and thus reduced oil production in Arabidopsis seeds [67].Mi-croRNA167 was identified to target the CsARF8 transcription factor in Camelina sativa, and CsARF8 upregulated the expression of the CsFAD3 gene by cooperating with bZIP67 and ABI3, thereby affecting ALA biosynthesis in C. sativa seeds [68].Increasing data indicated that plant seed oil biosynthesis and accumulation were controlled by a complex and multilevel regulatory mechanism, particularly a network of interacting transcriptional activators and repressors [69].Our study identified PfbZIP85 as a negative regulator in perilla seed oil biosynthesis, showing that PfbZIP85 can be a target in genetic engineering for the improvement of oil yield and quality in heterogenous hosts.Further research needs to address whether other TFs or miRNAs and even epigenetic regulators interact with PfbZIP85 and to identify more target genes of PfbZIP85, which will deepen our understanding of the PfbZIP85-mediated internet responsible for FA/oil biosynthesis during seed development and other biological processes.

Biological Materials
The high-oil-content perilla (Perilla frutescens) variety 'Jinzisu 1' was selected for this study and grown in Taigu District, Shanxi Province, China (112 • 58 ′ E, 37 • 42 ′ N).Seeds of 'Jinzisu 1' were harvested at 10, 20, and 30 days after flowering (DAF).All samples were promptly flash-frozen using liquid nitrogen and subsequently stored at −80 • C for further experiments.The tobacco species Nicotiana benthamiana was employed for protein subcellular localization in this study, while the common tobacco species Nicotiana tabacum was utilized for gene transformation.The growth conditions of all the tobacco plants included a photoperiod of 16 h of light and 8 h of darkness at 25 The bacterial and yeast strains, as well as the plasmids used in this work, are presented in Table S6.

Identification and Chromosomal Localization of bZIP Gene Family Members in P. frutescens
The genome annotation data for P. frutescens were obtained from the Perilla frutescens var.frutescens genome database (https://www.ncbi.nlm.nih.gov/genome/?term=txid48386(accessed on 9 March 2023)).AtbZIP sequences from Arabidopsis were acquired from the Arabidopsis Information Resource (TAIR) website (https://www.arabidopsis.org/index.jsp(accessed on 9 March 2023)).Then, all the candidate PfbZIPs were identified by the online tools NCBI CD-Search (https://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi (accessed on 10 March 2023)) and SMART database (http://smart.embl-heidelberg.de/(accessed on 10 March 2023)).ProtParam from ExPasy online tools was utilized to analyze the physicochemical properties of the identified PfbZIP members.The chromosomal locations of all the PfbZIP genes were obtained from the genome annotation data of P. frutescens.MapChart 2.32 was subsequently used to map the physical location of PfbZIP genes on the chromosome from the short-arm telomeres to the long-arm telomeres [6,55].

Multiple Sequence Alignment and Construction of a Phylogenetic Tree
Multiple sequence alignments of the PfbZIP proteins were conducted using Jalview 2.11.2.7 software.According to the alignment of the bZIP conserved domains between Pf-bZIPs and AtbZIPs, the neighbor-joining method (N-J) was employed to establish a phylogenetic tree utilizing MEGA 11.0.9 software, and the bootstrap test was set to 1000 times [6,12].Finally, all the confirmed PfbZIP members were divided into different groups based on the grouping of AtbZIP members.

Analysis of Gene Duplication Events
Segmental duplication analysis of the P. frutescens genome was conducted by MCScanX (Multiple Collinearity Scan Tool Kit) in TBtools 2.0, and the entire analytic process was executed with default settings.The tandem duplication event is defined as the occurrence of two or more genes within 200 kb on the same chromosome [60].The synteny relationships between the genomes of P. frutescens and two distinct species, A. thaliana and S. indicum, were identified and analyzed.The S. indicum data was obtained from the NCBI GenBank database (https://www.ncbi.nlm.nih.gov/genome/11560?genome_assembly_id=49670 (accessed on 13 March 2023)).

GO Annotation and KEGG Enrichment Analysis
To confirm the Gene Ontology (GO, http://www.geneontology.org/(accessed on 14 March 2023)) terms among all the PfbZIP genes in the database, we mapped each term and subsequently calculated the number of PfbZIP genes linked to each GO term.A list of genetic variations was generated based on their functional annotation in the GO database, and the numbers of PfbZIP genes were tallied separately.The hypergeometric test was applied to identify significantly enriched GO terms (FDR < 0.05) among PfbZIP gene members in comparison with the background, thereby determining the major functions of different PfbZIP genes.
The Kyoto Encyclopedia of Genes and Genomes (KEGG, http://www.kegg.jp/(accessed on 14 March 2023)) database facilitates the comprehensive exploration of gene functions, genomic interactions, and functional annotations.Genes can be classified by the pathways or by the functions they are involved in using the KEGG database.The hypergeometric test was applied to identify significantly enriched pathways (FDR < 0.05) among PfbZIP gene members in comparison with the background, thereby determining the major metabolic and signal transduction pathways in which different PfbZIP genes are involved.

Expression Profiling of PfbZIP Genes Based on RNA-Seq and RT-qPCR
To investigate the expression profiles of all the PfbZIP genes in developing perilla seeds, we obtained the transcriptome profiles of PfbZIP genes from the internal transcriptome sequencing database in our lab.Subsequently, we extracted the FPKM value (number of fragments per kilobase exon per million fragments), and then a heat map illustrating their expression patterns was generated using TBtools 2.0.
Total RNA from perilla-developing seeds was extracted utilizing the EASY spin Plus Plant RNA kit (Aidlab Biotechnologies Co., Ltd., Beijing, China).The first-strand cDNAs were generated using the StarScript II RT Mix with gDNA (GenStar BioSolutions, Beijing, China) following the manufacturer's instructions.Primer sequences were provided in Table S7.RT-qPCR amplification reactions were conducted via the TB Green ® Premix Ex Taq™ II (Tli RNaseH Plus) (TaKaRa, Beijing, China).The experiments were conducted on a CFX96 PCR system (Bio-Rad, Hercules, CA, USA).The PfActin gene was used as the internal reference gene [6].The test was performed using three independent biological samples with three technical replicates.Finally, the relative expression level was calculated by the 2 −∆∆Ct method [70].

Prediction of Target Genes Regulated by the bZIP Transcription Factor
To explore the regulatory role of PfbZIP TFs on the expressions of genes related to lipid/oil metabolism, a set of oil-related genes was selected for promoter cis-element analysis.The 2000 bp promoter regions upstream for these selected genes were obtained through TBtools 2.0, and then cis-acting element examination was conducted using the PlantCARE database (https://bioinformatics.psb.ugent.be/webtools/plantcare/html/(accessed on 20 March 2023)) [12].The identification of target genes was conducted by exploiting the specific recognition and binding capability of bZIP TFs to the A/C/T/CACGTG/C/T/A or GCCACGTGGA motif sequences [22,25].We further analyzed the expression correlation between these oil-related genes and PfbZIP TFs using their FPKM values.

Gene Cloning and Plasmid Construction
Gene-specific primers (primer sequences provided in Table S7) were designed according to the CDS sequences of the PfbZIP52 and PfbZIP85 genes.The TransStart ® FastPfu Fly DNA Polymerase (TransGen Biotech, Beijing, China) was utilized for the RT-PCR amplification reactions.The RT-PCR amplicons of PfbZIP52 and PfbZIP85 genes were ligated into the pGADT7 prey vector (Figure S3) utilizing the ClonExpress Ultra One Step Cloning Kit (Vazyme, Nanjing, China) through the one-step cloning method.Subsequently, these constructs were transformed into competent cells of Escherichia coli DH5α [6].The positive clones were identified via PCR and gene sequencing alignment (Tsingke Biotechnology Co., Ltd., Xi'an, China).
The specific sequences of the promoter region of PfGPAT1 and PfLPAT1B genes containing ACGT elements were synthesized by Nanjing Ruiyuan Biotechnology Co., Ltd.(Nanjing, China), and the synthesized sequences were separately ligated into the pHIS2 vector to construct bait vectors pHIS2-proPfGPAT1 and pHIS2-proPfLPAT1B, respectively (Figure S3).
Similarly, PfbZIP85 CDS was cloned and then individually inserted into three expression vectors, including the expression vector pCAMBIA1300/GFP carrying the GFP signal protein, the constitutive plant overexpression vector pCAMBIA1303, and the seedspecific overexpression vector pJC-Gly-DSRB using one-step cloning (the primer sequences are shown in Table S7) to form the expression vectors pCAMBIA1300-PfbZIP85/GFP, pCAMBIA1303-PfbZIP85, and pJC-Gly-DSRB-PfbZIP85 (Figure S3), respectively.
The promoter sequence of the PfLPAT1B gene was cloned from perilla by RT-PCR using total DNA and subsequently inserted into the expression vector pCAMBIA1301 to obtain a recombinant plasmid pCAMBIA1301-proPfLPAT1B (Figure S3).

The Yeast One-Hybrid (Y1H) Assay
The yeast one-hybrid (Y1H) assay was performed following the procedures described by Clontech (Takara).Bait vectors (pHIS2-proPfGPAT1 or pHIS2-proPfLPAT1B) and the AD plasmid (pGADT7) were transformed into Y187 yeast strain competent cells and cultured on SD-TL (Coolaber Technology Company, Beijing, China) medium at 30 • C for 3 d.pHIS2-P53 and pGAD53m were co-transfected into the yeast cell as the positive controls.Similarly, pHIS2-proPfGPAT1 + pGADT7-PfbZIP52 and pHIS2-proPfLPAT1B + pGADT7-PfbZIP85 were co-transformed into the yeast cell as the experimental group, respectively.
The concentration of 3AT for screening the positive colonies was determined by the self-activation detection concentration of 3AT of the pHIS2-proPfGPAT1 and pHIS2-proPfLPAT1B bait vectors.Each sample of pHIS2-proPfGPAT1 + pGADT7-PfbZIP52 or pHIS2-proPfLPAT1B + pGADT7-PfbZIP85 was randomly selected and then spotted on SD-TL and SD-TLH with or without an appropriate concentration of 3AT medium for 3 d to 5 d cultivation.

Subcellular Localization of PfbZIP85 Protein and GUS Assay
To investigate the subcellular localization of PfbZIP85 protein, the recombinant fusion plasmid 35S::PfbZIP85::GFP (pCAMBIA1300-PfbZIP85/GFP) and the control plasmid 35S::GFP were transiently expressed in N. benthamiana leaf epidermal cells through Agrobacterium-mediated transformation [6].After the tobacco plants were grown at 25 • C for more than 36 h, the transfected tobacco leaf samples were treated with DAPI reagent (Solarbio Life Sciences, Beijing, China), followed by observation of fluorescence signals utilizing a laser scanning confocal microscope (Leica TCS SP8).

GUS Stain and GUS Activity Assays
Agrobacterium GV3101 strain harboring 35S::PfbZIP85 and proPfLPAT1B::GUS (pCAMBIA1301-proPfLPAT1B) plasmids were transiently co-infiltrated into tobacco leaves.At the same time, the proPfLPAT1B::GUS plasmid alone was infiltrated into tobacco leaves as the control.After 48 h of culturing, the infiltrated leaves were subjected to GUS staining with a kit (Beijing Huayueyang Science and Technology Co., Ltd., Beijing, China), followed by observation under a stereoscopic microscope.Moreover, an RT-qRCR assay was employed to assess the relative expression level of the GUS gene.

Heterologous Overexpression of PfbZIP85 in Tobacco Plant
The recombinant plant overexpression vector pCAMBIA1303-PfbZIP85 and the seedspecific vector pJC-Gly-DSRB-PfbZIP85 were genetically transformed in tobacco by the Agrobacterium-mediated method, respectively.The leaves of aseptic tobacco seedlings were transformed via Agrobacterium infiltration [71].And then, the positive transgenic tobacco plants were identified using RT-PCR (primer sequences seen in Table S7).Subsequently, the positive transgenic tobacco plants were selected for phenotypic assessment.

Lipid Extraction and Fatty Acid Analysis
Total lipids were extracted from seeds or leaf tissues using chloroform-methanol-KCl (2:1:1, v/v/v) according to the method of Vanhercke et al. [13].The specific operation is carried out according to the following steps: Freeze-dried perilla seeds, tobacco seeds, and leaf tissues were transferred to a 10 mL stopper glass test tube containing a chloroformmethanol mixture and mixed with shaking on a vortex mixer for 10 min, and then 0.1 M KCl was supplemented and mixed for a further 5 min.Finally, the mixture was centrifuged at 4000 rpm for 10 min to collect the lower lipid phase.The remaining phase was washed once with chloroform, and the lipid phase was subsequently combined with the earlier extract.The collected chloroform was completely evaporated to dryness with nitrogen gas (N 2 ) and stored at −20 • C until further use.
Neutral lipid classes (TAG) were separated from total lipids by thin-layer chromatography (TLC) using a silica gel plate (100 mm × 200 mm, 0.20-0.25 mm thickness) with the developing agent of hexane-methyl tert-butyl ether-acetic acid (80:20:2, v/v/v), and then visualized by staining with iodine vapor.The TAG strip on the silicone plate was carefully scraped off using a blade and transferred into a stopper glass test tube, and then the fatty acid methyl ester (FAME) was prepared following the modified methods by Li et al. [72].0.5 mL of sodium methanolic solution (containing 0.001% BHT) was added to the aforementioned glass test tube, followed by the addition of tri-heptadecanoin (tri-17:0) (10 mg/mL in chloroform) as an internal standard.The test tube was sealed and incubated at 80 • C for 2 h.After the test tube containing the mixture was cooled, 0.5 mL of hexane (containing 0.001% BHT) and 1 mL of 0.9% KCl solution were added to each test tube and then mixed well.The mixture was centrifuged at 4000 rpm for 8 min.The top layer was collected and then completely evaporated to dryness with N 2 , followed by the addition of 0.2 mL of hexane to dissolve the extract and transferring into GC auto-sampler vials.
FAMEs were detected and analyzed utilizing an Agilent 7890B gas chromatograph (GC) equipped with a hydrogen flame detector and a G3903-63011 column (30 m × 0.25 mm × 0.25 µm).The initial temperature was 50 • C for 0.5 min, then to 194 • C at 30 • C/min, holding for 3.5 min, and then to 240 • C at 5 • C/min, holding for one min.The temperature of the FID detector was set at 280 • C, with hydrogen flowing at a rate of 40 mL/min, air at 400 mL/min, and nitrogen at 25 mL/min.The evaporator temperature was set at 250 • C. The split flow was not used, and the injection volume was 1 µL.The areas for each fatty acid, including the tri-17:0 standard, were collected and subsequently used to calculate the TAG content (µg/mg or µg/seed) and each fatty acid level (% of TAG).

Analysis of Other Agronomy Traits in Transgenic Tobacco Lines
The starch, protein, and soluble sugar contents of PfbZIP85-expressing tobacco plants were determined using assay kits specific for starch, protein, and soluble sugar content (Beijing Solarbio Science and Technology Co., Ltd., Beijing, China), respectively.In addition, the leaf dry weight, photosynthetic rate (Pn), thousand-seed weight, and germination rate of PfbZIP85-expressing plants were detected quantitatively.

Data Analysis
All samples were tested in triplicate, at least.The software DPS (new version 9.01) was used to statistically analyze the data with the single-factor multiple comparison method.Values are presented as mean ± SD (n = 3).Different lowercase letters indicate significant differences between treatments at p < 0.05.

Conclusions
In the present study, 101 PfbZIP TF members were first identified in the P. frutescens genome, being classified into eleven different groups (Group A, B, C, D, E, F, G, H, I, S, and UC) based on phylogenetic, gene structure, and protein conserved motif analysis.The diverse expression patterns were detected for different PfbZIP genes during perilla seed development.Particularly, PfbZIP52 expression exhibited a positive correlation with that of the PfGPAT1 gene, whereas the expression of PfbZIP85 displayed a significantly negative correlation with that of the PfLPAT1B gene.The Y1H assay and GUS activity test revealed that PfbZIP85 TF negatively regulated PfLPAT1B expression through physical interaction with the promoter of the PfLPAT1B gene.Functional characterization of PfbZIP85 in heterogeneous tobacco plants evidenced that PfbZIP85 mediated regulation of FA/oil biosynthesis and accumulation by modulating expressions of the lipid-related enzyme genes.These findings provide a valuable foundation for further functional examination of PfbZIP members, advancing our understanding of the PfbZIP-mediated regulation network for the biosynthesis of vegetable oils enriched with target FAs.

Figure 1 .
Figure 1.Phylogenetic tree of bZIP members from P. frutescens and Arabidopsis.The PfbZIP proteins (blue solid circle) and AtbZIP proteins (red solid circle) were classified into distinct groups in the phylogenetic tree.Different colors on the periphery indicate the distinct subgroups of bZIP proteins.

Figure 1 .
Figure 1.Phylogenetic tree of bZIP members from P. frutescens and Arabidopsis.The PfbZIP proteins (blue solid circle) and AtbZIP proteins (red solid circle) were classified into distinct groups in the phylogenetic tree.Different colors on the periphery indicate the distinct subgroups of bZIP proteins.

Figure 2 .
Figure 2. Multiple sequence alignments of the PfbZIP protein domains from P. frutescens.The basic region (BR) and leucine zipper (LZ) are shown by solid and dotted lines, respectively.

Figure 2 .
Figure 2. Multiple sequence alignments of the PfbZIP protein domains from P. frutescens.The basic region (BR) and leucine zipper (LZ) are shown by solid and dotted lines, respectively.

Figure 3 .
Figure 3. Synteny analysis of bZIP members between P. frutescens and the other two plant species.(A) Synteny examination of inter-chromosomal associations of PfbZIP genes.All PfbZIP gene pairs in the P. frutescens genome were indicated by red lines.(B) Synteny of bZIP members between P. frutescens, A. thaliana, and S. indicum.The synteny bZIP gene pairs between P. frutescens, A. thaliana, or S. indicum were emphasized using red lines.The collinear blocks of other genes between P. frutescens and A. thaliana, or S. indicum, were shown with gray lines.

Figure 3 .
Figure 3. Synteny analysis of bZIP members between P. frutescens and the other two plant species.(A) Synteny examination of inter-chromosomal associations of PfbZIP genes.All PfbZIP gene pairs in the P. frutescens genome were indicated by red lines.(B) Synteny of bZIP members between P. frutescens, A. thaliana, and S. indicum.The synteny bZIP gene pairs between P. frutescens, A. thaliana, or S. indicum were emphasized using red lines.The collinear blocks of other genes between P. frutescens and A. thaliana, or S. indicum, were shown with gray lines.

Figure 4 .
Figure 4. GO and KEGG enrichment analysis and expression profiles of PfbZIP genes during perilla seed development.(A) The distinct seed developmental stages of the perilla variety 'Jinzisu 1'.(B) GO enrichment analysis of PfbZIP gene family members.(C) KEGG enrichment analysis of PfbZIP gene family members.(D) Heat map of the PfbZIP gene expression patterns in developing seeds of P. frutescens.(E) The relative expression levels of the selected PfbZIP genes were detected by RT-qPCR in seed development.Values are presented as mean ± SD (n = 3).

Figure 4 .
Figure 4. GO and KEGG enrichment analysis and expression profiles of PfbZIP genes during perilla seed development.(A) The distinct seed developmental stages of the perilla variety 'Jinzisu 1'.(B) GO enrichment analysis of PfbZIP gene family members.(C) KEGG enrichment analysis of PfbZIP gene family members.(D) Heat map of the PfbZIP gene expression patterns in developing seeds of P. frutescens.(E) The relative expression levels of the selected PfbZIP genes were detected by RT-qPCR in seed development.Values are presented as mean ± SD (n = 3).

Figure 5 .
Figure 5. Prediction and interaction analysis of candidate PfbZIP TF-regulated target genes involved in lipid biosynthesis.(A) Total lipid dynamic accumulation in the developing seed of perilla.The total lipid contents are expressed by the mass of esterified fatty acids.(B) Heat map of expression correlation between eight PfbZIP TFs and key lipid-related enzyme genes.Red indicates a positive correlation, while blue indicates a negative correlation.* represents a significant difference at p < 0.05.** represents a significant difference at p < 0.01.*** represents a significant difference at p < 0.001.(C) Yeast one-hybrid assay of PfbZIP52 and PfbZIP85 with promoters of the PfGPAT1 and PfLPAT1B genes, respectively.

Figure 5 .
Figure 5. Prediction and interaction analysis of candidate PfbZIP TF-regulated target genes involved in lipid biosynthesis.(A) Total lipid dynamic accumulation in the developing seed of perilla.The total lipid contents are expressed by the mass of esterified fatty acids.(B) Heat map of expression correlation between eight PfbZIP TFs and key lipid-related enzyme genes.Red indicates a positive correlation, while blue indicates a negative correlation.* represents a significant difference at p < 0.05.** represents a significant difference at p < 0.01.*** represents a significant difference at p < 0.001.(C) Yeast one-hybrid assay of PfbZIP52 and PfbZIP85 with promoters of the PfGPAT1 and PfLPAT1B genes, respectively.

Figure 6 .
Figure 6.(A) Subcellular localization of PfbZIP85 in tobacco leaf cells.The fluorescence signals were observed using a laser-scanning confocal microscope (Leica TCS SP8).Scale bars = 50 µm.(B) GUS staining in the infiltrated tobacco leaves.Left, tobacco leaves infiltrated with the proPfLPAT1B::GUS plasmid alone.Right, tobacco leaves co-infiltrated with 35S::PfbZIP85 and proPfLPAT1B::GUS plasmids.(C) Expression analysis of the GUS gene in the transiently infected tobacco leaves.Values are presented as mean ± SD (n = 3).'a' and 'b' indicate significant differences at p < 0.05.

Figure 6 .
Figure 6.(A) Subcellular localization of PfbZIP85 in tobacco leaf cells.The fluorescence signals were observed using a laser-scanning confocal microscope (Leica TCS SP8).Scale bars = 50 µm.(B) GUS staining in the infiltrated tobacco leaves.Left, tobacco leaves infiltrated with the proPfLPAT1B::GUS plasmid alone.Right, tobacco leaves co-infiltrated with 35S::PfbZIP85 and proPfLPAT1B::GUS plasmids.(C) Expression analysis of the GUS gene in the transiently infected tobacco leaves.Values are presented as mean ± SD (n = 3).'a' and 'b' indicate significant differences at p < 0.05.

Figure 7 .
Figure 7. Analysis of TAG content and major FAs in TAG in the transgenic tobacco lines.(A) Transgenic tobacco plants.(B,C) Contents of total TAG and key TAG-associated FAs in PfbZIP85-expressing tobacco leaves.(D) Transgenic tobacco seeds.(E,F) Contents of total TAG and key TAG-associated FAs in PfbZIP85-expressing tobacco seeds.LDW, the dry weight of tobacco leaves.WT, untransformed tobacco plant.OE-1/-2/-3, the transgenic tobacco lines overexpressing the PfbZIP85

Figure 7 .
Figure 7. Analysis of TAG content and major FAs in TAG in the transgenic tobacco lines.(A) Transgenic tobacco plants.(B,C) Contents of total TAG and key TAG-associated FAs in PfbZIP85-expressing tobacco leaves.(D) Transgenic tobacco seeds.(E,F) Contents of total TAG and key TAG-associated FAs in PfbZIP85-expressing tobacco seeds.LDW, the dry weight of tobacco leaves.WT, untransformed tobacco plant.OE-1/-2/-3, the transgenic tobacco lines overexpressing the PfbZIP85 gene.The TAG contents are expressed by the mass of esterified fatty acids.Values are presented as mean ± SD (n = 3).Different lowercase letters indicate significant differences at p < 0.05.

Figure 9 .
Figure 9. Expression analysis of genes associated with FA/oil biosynthesis in the transgenic tobacco plant overexpressing PfbZIP85.The N. tabacum actin gene was used as the internal control gene.WT, untransformed tobacco plant.OE-1/-2/-3, the PfbZIP85-expressing tobacco lines.Values are presented as mean ± SD (n = 3).Different lowercase letters indicate significant differences between different samples at p < 0.05.

Figure 9 .
Figure 9. Expression analysis of genes associated with FA/oil biosynthesis in the transgenic tobacco plant overexpressing PfbZIP85.The N. tabacum actin gene was used as the internal control gene.WT, untransformed tobacco plant.OE-1/-2/-3, the PfbZIP85-expressing tobacco lines.Values are presented as mean ± SD (n = 3).Different lowercase letters indicate significant differences between different samples at p < 0.05.

Figure 10 .
Figure 10.Mechanistic model of FA/TAG biosynthesis mediated by the PfbZIP85 TF.For simp only one TAG molecule is displayed, and certain intermediates or reactions are omitted.Th downward arrow indicates the reduction in oil content.

Figure 10 .
Figure 10.Mechanistic model of FA/TAG biosynthesis mediated by the PfbZIP85 TF.For simplicity, only one TAG molecule is displayed, and certain intermediates or reactions are omitted.The blue downward arrow indicates the reduction in oil content.

Table 1 .
Prediction of cis-elements in promoter regions of genes related to FA biosynthesis in perilla.