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Article

Genome-Wide Identification and Expression Analysis of Auxin Response Factor (ARF) Gene Family in Longan (Dimocarpus longan L.)

by
Yuan Peng
1,2,†,
Ting Fang
1,2,†,
Yiyong Zhang
1,2,
Mengyuan Zhang
1,2 and
Lihui Zeng
1,2,*
1
College of Horticulture, Fujian Agriculture and Forestry University, Fuzhou 350002, China
2
Institute of Genetics and Breeding in Horticultural Plants, Fujian Agriculture and Forestry University, Fuzhou 350002, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Plants 2020, 9(2), 221; https://doi.org/10.3390/plants9020221
Submission received: 18 January 2020 / Revised: 5 February 2020 / Accepted: 5 February 2020 / Published: 8 February 2020
Browse Figures
Versions Notes

Abstract

:
Auxin response factor (ARF) is the key regulator involved in plant development. Despite their physiological importance identified in various woody plants, the functions of ARF genes in longan were still not clear. In this study, 17 longan ARF genes (DlARF) were identified using the reference longan genome data. According to the phylogenetic relationships among longan, Arabidopsis and apple, DlARFs were divided into four classes. Most DlARFs showed a closer relationship with ARFs from apple than those from Arabidopsis. The analysis of gene structure and domain revealed high similarity of different ARF genes in the same class. Typical features of B3-type DNA binding domain (DBD) motif, Auxin Resp motifs, and a highly conserved C-terminal Phox and Bem1 (PB1) domain were present in all DlARFs except for DlARF-2,-3,-13 which lacked PBI domain. Expression profiles of 17 DlARF genes in longan different tissues showed that some DlARF genes were tissues-specific genes. Analysis of three longan transcriptomes showed seven DlARFs (DlARF-1,-2,-6,-8,-9,-11,-16) had higher expression levels during floral bud differentiation of common longan and in the buds of ‘Sijimi’, suggesting these genes may promote floral bud differentiation in longan. Further qPCR analysis showed that among seven DlARF genes, the expression levels of DlARF-2,-6,-11,-16 increased significantly during the physiological differentiation stage of longan floral buds, confirming that they may play a role in flowering induction. Promoter sequence analysis revealed cis-elements related to flowering induction such as low-temperature responsiveness motif and circadian control motif. Motifs linked with hormone response for instance Auxin, MeJA, Gibberellin, and Abscisic acid were also found in promoters. This study provides a comprehensive overview of the ARF gene family in longan. Our findings could provide new insights into the complexity of the regulation of ARFs at the transcription level that may be useful to develop breeding strategies to improve development or promote flowering in longan.

1. Introduction

Auxin is a vital regulator of plant growth, and plays important roles not only in diverse aspects of plant development such as control of leaf vascular patterning [1], apical dominance [2], establishment of embryonic axis [3], and root geotropism phototropism of the stem [4], but also in fruit development and controlling circadian flower opening and closure [5,6]. Indeed, different growth regulators influenced flower formation, which are dependent on the physiological stage of the explant, particularly its endogenous hormone levels [7]. Previously, the floral transition will be initiation by an endogenous increase in the levels of indole-3-acetic acid (IAA) influenced by Thidiazuron of Dendrobium [8]. Over the past 30 years, it has been clearly certificated that auxins can exert rapid and specific effects on genes at the molecular levels [9]. Many gene families, such as auxin/indole-3-acetic acid (Aux/IAA), gretchen hagen 3 (GH3), small auxin-up RNA (SAUR), and auxin response factor (ARF), were involved in auxin signal transduction, forming a complex auxin signal regulation network at the molecular level [10]. In this regulatory pathway, ARF is an important transcription factor family, which DNA binding domain (DBD) can specifically bind to TGTCTC auxin response elements (AuxREs) in the target gene promoter to participate in auxin signal transduction and regulate auxin responsive genes expression [11]. A working model for ARF activation responses to auxin is now well-established [12]. Under lower auxin concentration, Aux/IAA proteins form dimers with ARFs proteins inhibit ARF activity by recruiting the co-repressor TOPLESS (TPL), which results in the repression of auxin responsive genes [13]. At higher auxin concentration, Aux/IAAs proteins bind to the SCFTIR1/AFB complex and rapidly become ubiquitinated and degraded, allowing ARFs to release and activate transcription of its target genes [14].
Considering the roles of ARFs in various physiological and developmental, ARF gene families have been identified and characterized in many plants such as Arabidopsis thaliana, potato (Solanum tuberosum), rice(Oryza sativa), papaya (Carica papaya), and chickpea (Cicer arietinum) [15,16,17,18,19]. Although biochemical and genetic analyses have established a crucial function for ARF genes in plant growth and development, current knowledge of the biological roles of individual ARFs is mainly from the characterization of model plants Arabidopsis, rice and tomato. In Arabidopsis, ARF2 regulates leaf senescence and floral organ abscission independently of the ethylene and cytokinin response pathways [20]; ARF6, NPH4/ARF7, and ARF8 affect leaf and inflorescence growth, promoting hypocotyl elongation [21,22]. In rice, negative regulation of OsARF18 expression by OsmiR160 is critical for rice normal growth and development [23]; OsARF12 is regarded as one of major player in phosphate-induced auxin responses, indicating that ARFs might be involved in phosphate homeostasis in crops [24]. In tomato, SlARF7 acts as a negative regulator of fruit set after pollination and fertilization, and moderates auxin response during fruit growth [25]; SlARF4 controls chlorophyll accumulation in fruit and down-regulation of SlARF4 results in a dark-green immature fruit phenotype with increased chloroplasts [26]. In addition, genome-wide identification and expression analyses of the ARF family suggest that the expression of many ARF genes is altered in various species in responsive to abiotic stresses, such drought, salt, or cold [27,28]. Together, ARF family genes play an important role in regulating plant growth and development, and in plant responses to multiple signaling transduction pathways. However, to our knowledge, ARF gene family of longan (Dimocarpus longan) still remains unexplored.
Longan is an important subtropical fruit tree of Sapindaceae family, which is grown in many subtropical and tropical countries with most of the production in Southeast Asia and Australia [29]. As an edible drupe fruit and source of traditional medicine, longan is grown in most areas of Southern China, including Guangdong, Guangxi, Fujian, Sichuan, Yunnan, and Hainan [30]. Considering the significance of ARFs in plant growth and development, information on ARF gene family of longan is needed for better understanding. In this study, a comprehensive analysis of ARF family genes was conducted in longan based on its genomic sequence and three transcriptome databases [31,32,33]. A total 17 Dimocarpus longan ARF (DlARF) genes were identified and their physical and chemical properties, conserved motifs, genomic structures, evolutionary relationship and functional classification were analyzed. Moreover, expression and promoter cis-acting elements of DlARF genes were investigated. Our results will provide valuable information for understanding the classification and putative functions of DlARFs and make more insight into the molecular basis of auxin responses in longan.

2. Materials and Methods

2.1. Plant Materials

Longan (cultivar ‘Honghezi’) plants are in experimental field of Fujian Agriculture and Forestry University. The shoot tips from branches that were expected to bloom were collected monthly over a period of 4 months from October 2018 to January 2019. The samples were stored at −80 °C.
‘Honghezi’ seedlings were grown for six month, which were used for hormonal treatments. Plants were treated with abscisic acid (ABA, 50 mM), methyl jasmonate (MeJA, 100 mM), gibberellic acid (GA3, 50 mM), and 6-benzylaminopurine (6-BA, 75 mM) for 4 h at 26 ± 2 °C, respectively. Five plants were used in each treatment. Meanwhile, five seedlings have no treatments as a control. The leaves were immediately frozen in liquid nitrogen and stored at −80 °C until RNA extraction. Collect three samples per treatment and each sample was made by pooling at least five plants.

2.2. Identification of ARF Genes in Dimocarpus Longan

The Arabidopsis ARFs (AtARFs) gene sequences were downloaded from NCBI gene database (https://www.ncbi.nlm.nih.gov) according to the Gene ID [9], the longan genomic were obtained from GigaScience (http://gigadb.org) and the apple (Malus domestica) ARFs family were loaded from GDR Gene Database (https://www.rosaceae.org). The Arabidopsis ARFs protein sequence were used as queries to search against longan genome and the putative genes were identified based on a local BLASTP search at the score value of e-30.0 value. The 17 longan ARF genes were further confirmed by the hidden Markov model (HMM) profiles of the ARF gene family which include B3 DNA binding (Pfam 02362), Auxin Resp (Pfam 06507), and PB1 domains (Pfam 02309). The molecular weight (MW) and isoelectric points (PI) of longan ARF family proteins were obtained from ExPASy tool [34], and the Amino-acid content of the MR domain in DlARFs was calculated using InterPro (http://www.ebi.ac.uk/interpro).

2.3. Sequence Alignment and Phylogenetic Tree

Multiple alignment of ARF proteins were analyzed by MUSCLE progress of MEGA6.0. Based on this alignment, a bootstrapped neighbor-joining (NJ) tree was constructed using MEGA (version 6.0) with the bootstrap test replicated 1000 times [35]. Classified and annotated of ARF protein sequences by using iTOL (https://itol.embl.de/itol.cgi).

2.4. Gene Structure and Domain Analysis of DlARFs

Conserved domains of DlARF proteins were identified using the InterPro, the original annotation file in gff3 format of longan genome was downloaded from GigaScience (http://gigadb.org), CDS and UTR domain of DlARFs were analyzed and annotated by TBtools [36]. The cis-acting elements of DlARFs gene promoter were analyzed using PlantCARE [37].

2.5. RNA Isolation and Quantitative Real Time (qRT-PCR)

RNA was extracted with EASY spin plus complex plant RNA kit provided by Aidlab company (Beijing, China), reverse transcription RNA into a single-stranded cDNA by using the PrimeScriptTM RT reagent kit and gDNA Eraser kit provided by TaKaRa. The primers were designed by DNAMAN8.0 software and tested to ensure amplification of single discrete bands with no primer-dimers. Product size from 140bp to 200bp. Primer sequences are shown in detail in the Supplementary Table S1. Longan actin gene was used as the reference gene for expression analyzing [38]. The qRT-PCR experiment used CFX96 real-time PCR Detection system (Bio-Rad laboratories, Hercules, CA, USA) and TB Green mixture (TaKaRa Bio, Shiga, Japan). The relative expression of specific gene was quantitated with the 2−ΔΔCt calculation method [39].

3. Results

3.1. Identification of DlARF Gene Family in Longan

A BLASTp search was implemented against the longan genome using Arabidopsis ARF genes as queries to perceive putative genes encoding the ARF. A total 17 ARF genes were identified in longan. All the high-quality reads of longan were assembled into 51,392 contigs and 17,367 scaffolds (≥200 bp) [31], 17 ARF genes were concentrated in the scaffold range from number 41 to 905. According to their position from the top to the bottom on the scaffold, 17 ARFs were named from DlARF1 to DlARF17 (Figure 1).
Physical and chemical properties of 17 DlARF genes were listed in Table 1, including isoelectric point (PI), molecular weight (MW) and coding sequence length (CDS). The length of 17 DlARF proteins varied from 575 (DlARF3) to 1498 aa (DlARF6), with an average of 845 aa. They had the lowest MW of 63.54 KDa (DlARF3) and the highest MW of 132.00 KDa (DlARF1), with an average of 93.86 KDa. The PI varied from 5.27 (DlARF16) to 8.03 (DlARF14), with an average of 6.39. Furthermore, all DlARF proteins are unstable, hydrophobic protein, suggesting that they might play roles in different subcellular environments.

3.2. Phylogenetic Analysis and Classification of DlARF Genes

To investigate the phylogenetic relationship of DlARFs, the neighbor-joining (NJ) method [35] was used to construct a phylogenetic tree consisting of 17 DlARFs, 21 AtARFs of Arabidopsis and 31 MdARFs of apple. The phylogenetic distribution indicated there were higher homologous between longan and apple, possibly due to they are both woody fruit trees, however, there still more than 50% homology between longan with Arabidopsis. All ARFs analyzed were divided into four classes (classⅠ, classⅡ, classⅢ, and classⅣ) (Figure 2). ClassⅠ contained the most ARF numbers (6 DlARFs, 8 MdARFs and 13 AtARFs) and was further divided into two subgroups. ClassⅡ included five DlARFs. ClassⅢ and classⅣ included one and four DlARFs, separately. DlARF13 was in an isolated branch which lacks of Arabidopsis orthologs.

3.3. Structure Analysis and Motif Composition of DlARF Genes

By comparing the corresponding genomic DNA sequences, exon and intron structures of DlARF genes were obtained. The results showed that different classes contained different exon numbers, ranging from 2 to 22 (Figure 3). For instance, there were 12–22 exons in DlARF-4,-6,-10,-11,-14, and -15 which were all grouped in classI. There were 13–18 exons in DlARF-1,-8,-9,-12 and DlARF-16 which belonged to classⅡ. DlARF2 in classⅢ contained 18 exons, and DlARF-3,-5,-7,-17 in class Ⅳ had the smallest number of exons which ranged from 2 to 4.
In addition to structural analysis, the pattern of conserved domains between ARF subclasses can also provide some clues on classification (Figure 4). It was reported that the typical features of ARF protein are B3-type DBD motif, Auxin Resp motifs, and a highly conserved C-terminal PB1 domain [15]. Our results showed that most of DlARF proteins had these three typical domains except for DlARF2 in class Ⅲ, DlARF3 in class Ⅳ, and DlARF13 which lacked C-terminal PB1 domain.

3.4. Expression Profiles of DlARF Genes in Different Plant Tissues

To explore the putative functions of DlARFs, FPKM (Fragments per Kilobase of transcript per million mapped reads) values were used to assess the expression pattern of 17 DlARF genes in nine different tissues of longan (Figure 5). The expression levels of DlARF-1,-6,-8,-11 were ubiquitously abundant in all tissues. DlARF1 had higher expression in stems and roots, DlARF6 had the higher expression levels in young fruits and pulp, DlARF8 had the highest expression level in pulp, whereas DlARF5 and DlARF14 were absent from nine tissues (FPKM value < 3). DlARF-3,-17,-13,-15 had lower expression levels in nine tissues (FPKM value < 30). DlARF-2,-4,-7 were tissue-specific genes, DlARF2 showed pericarp-specific expression, DlARF4 showed root-specific expression, while DlARF7 was leaf-specific gene.

3.5. Expression Profiles of DlARF Genes in Different Longan Varieties

‘Shixia’ and ‘Lidongben’ are common longan varieties exhibiting seasonal flowering traits, while ‘Sijimi’ is a specific variety with continuous flowering trait. Firstly, the expression patterns of 17 DlARF genes were analyzed using RNA-seq databases of apical buds during floral bud development in ‘Shixia’ [33]. In Guangdong Province of China, apical buds in November are at the stage of before the emergence of floral primordia, apical buds in December are at the stage of floral organ differentiation which is characterized by the appearance of red dot, and apical buds in January is characterized by the appearance of the first inflorescence [33]. The results showed that there were nine DlARFs (DlARF-1,-2,-4,-6,-8,-9,-10,-11,-16) that showed higher transcript levels in November and December in ‘Shixia’ (Figure 6a). In addition, the expression levels of 17 DlARFs were compared between ‘Sijimi’ and ‘Lidongben’ using the RNA-seq databases, which were collected from apical buds of grafting newly-sprouting [32] (Figure 6b). The results showed that seven DlARFs (DlARF-1,-2,-6,-8,-9,-11,-16) had higher expression levels in ‘Sijimi’ than in ‘Lidongben’. Taken together, seven genes (DlARF-1,-2,-6,-8,-9,-11,-16) showed higher expression in both analyses.

3.6. Expression Patterns of Seven DlARF Genes during Floral Bud Physiological Differentiation of Longan

Real-time qPCR was performed further to explore the expression patterns of seven DlARF genes (DlARF-1,-2,-6,-8,-9,-11, -16) during floral bud physiological differentiation of longan (Figure 7). In Fujian Province, China, the physiological differentiation stage of longan floral buds is in November and December [40]. The expression of DlARF-2,-6,-11 showed a trend of increasing first and then decreasing, peaking in the November or December. DlARF16 showed the opposite tendency, the expression level decreased in December and increased significantly in January. The transcript levels of DlARF1 and ARF18 did not change obviously from October to January.

3.7. Cis-Element Prediction in Promoters of Seven DlARF Genes

The distribution of cis-elements may reflect the potential up-stream regulatory factors of genes. Thus, the 1500 bp upstream sequence of DlARF-1,-2, -6, -8, -9,-11, -16 was obtained from the longan genome and analyzed, the putative cis-elements of these promoters were shown in Table S2.
Cis-elements related to circadian control were found in DlARF-6,-8,-9,-11 promoters. In addition, an LTR motif related to low-temperature responsiveness was also found in the promotor of DlARF-1,-8,-9. Among seven promoters, five promoters (DlARF-6,-8,-9,-11,-16) contained one or more AuxREs motif. CGTCA/TGACG motif involved in MeJA responsiveness was found in the promotor sequence of DlARF-6,-8,-11,-13,-16. DlARF-1,-6 had GARE-motif, which involved in gibberellin responsive. The promoter of DlARF-1,-2,-6,-9,-16 had ABRE motif, which involved in abscisic acid responsiveness.

3.8. Expression Patterns of Seven DlARFs with Hormone Treatments

Hormones play a very important role in the process of flowering [41]. Hormone-response motifs were found in the promoters of DlARFs, therefore the expression of seven DlARF genes in response to hormone treatments was investigated by qRT-PCR (Figure 8). The results showed that the expression levels of all seven DlARF genes declined in response to different hormone treatments. DlARF-1,-6,-9,-11 had a significant decrease in expression levels.

4. Discussion

Auxin influences developmental processes from embryogenesis to senescence in plants, including that causing apical dominance, controlling embryo development, and promoting the floral transition [41,42,43]. ARFs is one of the important transcriptional regulator families to regulating the auxin transduction [15,44].
In this study, 17 DlARFs were identified in longan. The comprehensive phylogenetic analysis showed that longan ARFs could be divided into four subgroups, the same as previous phylogenetic classifications of ARFs in other species such as apple, banana [18], Arabidopsis [15], and rice [17].
The identification and classification of the DlARF gene family was supported by gene structure and conserved domain analyses. ARF proteins in higher plants are composed of three modular and portable domains, which range in size from 69 to 129 kDa and are defined by their N-terminal DBD [45]. The typical ARF protein contains a conserved N-terminal B3-type DBD, which is required for efficient binding to AuxRE [9], a variable middle region (MR) that functions as an activation domain (AD) or repression domain (RD), and a carboxyl-terminal Phox and Bem1 (PB1) domain (CTD: domain III/IV), which is involved in protein–protein interactions by dimerizing with auxin/indole-3-acetic acid (Aux/IAA) family genes as well as ARFs [15,46]. All DlARFs have a typical DBD domain. Additionally, most DlARFs contain a CTD domain, suggesting they can form dimers with ARFs or Aux/IAA proteins.
ARF binds to AuxRE motif in the promoters of auxin-regulated genes by activating (AD domain) or repressing (RD domain) which depend on a middle domain (MR) [47]. In Arabidopsis, the AD is enriched in glutamine (Q), leucine (L) and serine (S) residues and the RD is enriched in glycine (G), leucine (L), serine (S), and proline (P) residues [48]. The detailed protein sequence analysis revealed that the glutamine (Q), leucine (L) and serine (S) regions were found in the MR of DlARF-1,-7,-9,-12,-16, indicating these genes were more likely acting as activators. On the other hand, DlARF-2,-6,10,-11,-13,-15 and DlARF17 were found to be rich in the glycine (G), leucine (L), serine (S), and proline (P) regions rich in the MR, indicating they are more likely acting as repressors. The activator/repressor ratio among DlARFs is 0.35, which is higher than that in Medicago (0.26) but lower than that in Arabidopsis (0.59). However, the mechanisms of activation and repression are still unclear [49].
Tissue expression analyses revealed that 17 DlARF genes had different expression patterns in different tissues. DlARF-6,-10,-11 which were clustered into classⅠ showed higher expression in leaf, pulp, and young fruit. In Arabidopsis, the functions of ARF genes in the same class were involved in controlling leaf senescence and floral organ abscission [20], so DlARF-6,-10,-11 might have similar functions in regulating leaf senescence. DlARF-1,-8,-9,-12,-16 in classⅡ showed higher expression in stem, root, and flower, there have been reported that AtARF genes in classⅡ played an important role in plant growth and development, such as regulating flower maturation and fertilization, promoting fruit development [22,50], therefore, they might also play an important role in flower growth. DlARF2 in classⅢ and DlARF-3,-5,-7,-17 in classⅣ showed lower expression in all nine tissues. There were few studies in the same category genes in Arabidopsis or apple, their functions remain unclear. DlARF13, a special gene, was clustered in an isolated class. DlARF13 shares 35% identity at the amino acid level with the Citrus sinensis ARF14 (Cs7g02210.1), which was also clustered to an isolated class [27] (Figure S1). This separated class is absent from herbaceous annual plants, such as Arabidopsis, cassava, and rice, but present in sweet orange and other woody perennials, so it might be a woody preferential specific clade [15,17,19].
It has been reported that free endogenous IAA was intimate correlated with the early stage of flower bud differentiation, high concentration of IAA, which act in apical bud will promote flowering. [36,51,52,53]. Seven DlARFs genes (DlARF-1,-2,-6,-8,-9,-11,-16) have been identified to show higher expression levels during longan floral bud induction and flower organ development. At the same time, these seven genes showed higher expression in the grafting newly-sprouting buds of ‘Sijimi’. ‘Sijimi’ has a continuous blossoming trait, the newly-sprouting buds in ‘Sijimi’ are speculated to have the capacity of continuous flowering after maturity [32]. These results suggest that these seven DlARF genes may play a role in promoting floral bud differentiation in longan. According to previous research, down-regulation of SlARF6 and SlARF8 by miR167 leads to floral development defects and female sterility in tomatoes. SlARF6 and SlARF8 have conserved roles in controlling growth and development of vegetative and flower organs in dicots [54]. DlARF8 and DlARF1, which were similar with tomato SlARF6 and showed a high expression in flowers, may have the same roles in controlling flower organ development.
Further analysis showed that the expression levels of DlARF-2,-6,-11,-16 increase significantly during the physiological differentiation stage of floral buds, indicating they might play an important role in flowering induction. In Arabidopsis, AtARF2 mRNA are present in roots, leaves and flowers [48], and promotes transitions between multiple stages of development [20,22]. DlARF6, a homologous gene of AtARF2, which expression increased during flower bud physiological differentiation period, peaked in November, may be similar with AtARF2, participating in the regulation of flowering transition. In Arabidopsis, AtARF1 acts in a partially redundant manner with AtARF2 [20]. The transcript of DlARF11 (homolog gene of AtARF1) also was abundant in the buds during the physiological differentiation period, suggesting it may have partially redundant manner with DlARF6. AtARF3 not only integrated the function of AGAMOUS (AG) and APETALA2 (AP2) in floral meristem determinacy [55], but also regulated floral meristem determinacy by repressing cytokinin biosynthesis and signaling [56]. DlARF2 (similar to AtARF3), showed high expression level during the flower bud differentiation, and it also highly expressed during the physiological differentiation stage, suggesting that DlARF2 might have the same function in floral meristem determinacy. AtARF5 (the homologous gene of DlARF16), is critically required for embryonic root and flower formation [57]. DlARF16 showed a higher expression level in flower and root, so it might play a role in root and flower development of longan.
Environmental conditions and endogenous circadian rhythms adjust the flowering time and thereby enable plants to reproduce. Low temperature is required for flowering induction in longan. Cis-elements analysis reveals some flowering-related motifs such as low-temperature respond and circadian control [58], suggesting these DlARFs response to low temperature and circadian rhythms and then regulate flowering. There was also an enrichment of cis-elements linked with hormone response. Many hormones have been reported to be involved in the regulation of flower opening or formation with relation to both internal and external cues, such as gibberellic acid, which is able to induce flowering at low temperature and control onset of flower formation in Arabidopsis. Jasmonic acid facilitates flower opening and floral organ development through the up-regulated expression of SlMYB21 in tomato [59,60,61]. The result of real time PCR experiment revealed seven DlARFs responded to cytokinin, MeJA, Gibberellin, and Abscisic acid. In potato, the expression of StARFs under various phytohormone treatments (GA3, ABA, auxin, cytokinin) were analyzed, most StARF members slightly decrease or even unchanged in response to hormones [16]. In sweet orange, CiARFs present at low levels at 6 h with the IAA treatment and up-regulated at 12 h by IAA and NPA treatments [27]. Our results are similar with CiARFs in response to 6 h IAA treatment.

Supplementary Materials

The following are available online at https://www.mdpi.com/2223-7747/9/2/221/s1, Table S1: The primer sequences of seven DlARFs and reference gene in longan, Table S2: Analysis of cis-elements in flower bud differentiation related ARF genes in longan, Figure S1: Protein sequences alignment between CiARF14 and DlARF13.

Author Contributions

Y.P., T.F., and L.Z. conceived and designed the analysis. Y.P., T.F., Y.Z., and M.Z. performed the analysis. Y.P. wrote and edited the manuscript and edited the manuscript. L.Z. and T.F. revised the manuscript. Y.P. and T.F. contributed equally to this manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Construction of Plateau Discipline of Fujian Province (102/71201801101).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Mattsson, J.; Ckurshumova, W.; Berleth, T. Auxin signaling in Arabidopsis leaf vascular development. Plant Physiol. 2003, 131, 1327–1339. [Google Scholar] [CrossRef] [Green Version]
  2. Phillips, I.D. Apical Dominance. Annu. Rev. Plant Physiol. 2003, 26, 341–367. [Google Scholar] [CrossRef]
  3. Robert, H.S.; Park, C.; Gutièrrez, C.L.; Wójcikowska, B.; Pěnčík, A.; Novák, O.; Chen, J.; Grunewald, W.; Dresselhaus, T.; Friml, J.; et al. Maternal auxin supply contributes to early embryo patterning in Arabidopsis. Nat. Plants 2018, 4, 548–553. [Google Scholar]
  4. Friml, J.; Wiśniewska, J.; Benková, E.; Mendgen, K.; Palme, K. Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis. Nature 2002, 415, 806. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Gong, H.; Peng, Y.; Zou, C.; Wang, D.; Xu, Z.; Bai, S. A simple treatment to significantly increase signal specificity in immunohistochemistry. Plant Mol. Biol. Rep. 2006, 24, 93–101. [Google Scholar] [CrossRef]
  6. Ke, M.; Gao, Z.; Chen, J.; Qiu, Y.; Zhang, L.; Chen, X. Auxin controls circadian flower opening and closure in the waterlily. BMC Plant Biol. 2018, 18, 143. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Shizufumi, T.; Atsushi, M.; Hiroshi, H. Regulation by Abscisic Acid of In Vitro Flower Formation in Torenia Stem Segments. Plant Cell Physiol. 1985, 26, 675–682. [Google Scholar]
  8. Ferreiraa, W.M.; Kerbauyb, G.B.; Krausb, J.E.; Pescadorc, R.; Suzuki, R.M. Thidiazuron influences the endogenous levels of cytokinins and IAA during the flowering of isolated shoots of Dendrobium. J. Plant Physiol. 2006, 163, 1126–1134. [Google Scholar] [CrossRef]
  9. Gretchen, H.; Tom, G. Auxin-responsive gene expression: Genes, promoters and regulatory factors. Plant Mol. Biol. 2002, 49, 373–385. [Google Scholar]
  10. Woodward Andrew, W.; Bonnie, B. Auxin: Regulation, Action, and Interaction. Ann. Bot. 2005, 95, 707–735. [Google Scholar] [CrossRef] [Green Version]
  11. Liscum, E.; Reed, J.W. Genetics of Aux/IAA and ARF action in plant growth and development. Plant Mol. Biol. 2002, 49, 387. [Google Scholar] [CrossRef] [PubMed]
  12. Mohammad, S.; Rammyani, B.; Mark, E. SCFTIR1/AFB-based auxin perception: Mechanism and role in plant growth and development. Plant Cell 2015, 27, 9–19. [Google Scholar]
  13. Szemenyei, H.; Hannon, M.; Long, J.A. TOPLESS Mediates Auxin-Dependent Transcriptional Repression During Arabidopsis Embryogenesis. Science 2008, 319, 1384–1386. [Google Scholar] [CrossRef] [PubMed]
  14. Wang, R.; Estelle, M. Diversity and specificity: Auxin perception and signaling through the TIR1/AFB pathway. Curr. Opin. Plant Biol. 2014, 21, 51–58. [Google Scholar] [CrossRef] [Green Version]
  15. Guilfoyle, T.J.; Hagen, G. Auxin response factors. Curr. Opin. Plant Biol. 2007, 10, 453–460. [Google Scholar] [CrossRef]
  16. Song, S.; Hao, L.; Zhao, P.; Zhong, Y.; Xu, N.; Zhang, H.; Liu, N. Genome-wide Identification, Expression Profiling and Evolutionary Analysis of Auxin Response Factor Gene Family in Potato (Solanum tuberosum Group Phureja). Sci. Rep. 2019, 9, 1755. [Google Scholar] [CrossRef]
  17. Wang, D.; Pei, K.; Fu, Y.; Sun, Z.; Li, S.; Liu, H.; Tang, K.; Han, B.; Tao, Y. Genome-wide analysis of the auxin response factors (ARF) gene family in rice (Oryza sativa). Gene 2007, 394, 13–24. [Google Scholar] [CrossRef]
  18. Liu, K.; Yuan, C.; Li, H.; Lin, W.; Yang, Y.; Shen, C.; Zheng, X. Genome-wide identification and characterization of auxin response factor (ARF) family genes related to flower and fruit development in papaya (Carica papaya L.). BMC Genom. 2015, 16, 901. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Die, J.V.; Gil, J.; Millan, T. Genome-wide identification of the auxin response factor gene family in Cicer arietinum. BMC Genom. 2018, 19, 301. [Google Scholar] [CrossRef] [Green Version]
  20. Ellis, C.M.; Nagpal, P.; Young, J.C.; Hagen, G.; Guilfoyle, T.J.; Reed, J.W. AUXIN RESPONSE FACTOR1 and AUXIN RESPONSE FACTOR2 regulate senescence and floral organ abscission in Arabidopsis thaliana. Development 2005, 132, 4563–4574. [Google Scholar] [CrossRef] [Green Version]
  21. Reed, J.W.; Wu, M.F.; Reeves, P.H.; Hodgens, C.; Yadav, V.; Hayes, S.; Pierik, R. Three Auxin Response Factors Promote Hypocotyl Elongation. Plant Physiol. 2018, 178, 864–875. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Nagpal, P.; Ellis, C.M.; Weber, H.; Ploense, S.E.; Barkawi, L.S.; Guilfoyle, T.J.; Hagen, G.; Alonso, J.M.; Cohen, J.D.; Farmer, E.E.; et al. Auxin response factors ARF6 and ARF8 promote jasmonic acid production and flower maturation. Development 2005, 132, 132–4107. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Huang, J.; Li, Z.; Zhao, D. Deregulation of the OsmiR160 Target Gene OsARF18 Causes Growth and Developmental Defects with an Alteration of Auxin Signaling in Rice. Sci. Rep. 2016, 6, 29938. [Google Scholar] [CrossRef] [PubMed]
  24. Attia, K.A.; Abdelkhalik, A.F.; Ammar, M.H.; Wei, C.; Yang, J.; Lightfoot, D.A.; El-Sayed, W.M.; El-Shemy, H.A. Antisense phenotypes reveal a functional expression of OsARF1, an auxin response factor, in transgenic rice. Curr. Issues Mol. Biol. 2009, 11 (Suppl. 1), i29. [Google Scholar]
  25. De Jong, M.; Wolters-Arts, M.; Feron, R.; Mariani, C.; Vriezen, W.H. The Solanum lycopersicum auxin response factor 7 (SlARF7) regulates auxin signaling during tomato fruit set and development. Plant J. 2010, 57, 160–170. [Google Scholar] [CrossRef] [PubMed]
  26. Brian, J.; Pierre, F.; Enrique, O.; Hicham, Z.; Li, Z.; Alain, L.; Claude, P.J.; Mondher, B. Down-regulation of DR12, an auxin response factor homolog, in the tomato results in a pleiotropic phenotype including dark green and blotchy ripening fruit. Plant J. 2002, 32, 603–613. [Google Scholar]
  27. Li, S.; OuYang, W.; Hou, X.; Xie, L.; Hu, C.; Zhang, J. Genome-wide identification, isolation and expression analysis of auxin response factor (ARF) gene family in sweet orange (Citrus sinensis). Front. Plant Sci. 2015, 6, 119. [Google Scholar] [CrossRef] [Green Version]
  28. Hu, W.; Zuo, J.; Hou, X.; Yan, Y.; Wei, Y.; Liu, J.; Li, M.; Xu, B.; Jin, Z. The auxin response factor gene family in banana: Genome-wide identification and expression analyses during development, ripening, and abiotic stress. Front. Plant Sci. 2015, 6, 742. [Google Scholar] [CrossRef] [Green Version]
  29. Matsumoto Tracie, K. Genes uniquely expressed in vegetative and potassium chlorate induced floral buds of Dimocarpus longan. Plant Sci. 2006, 170, 500–510. [Google Scholar] [CrossRef]
  30. Park, S.J.; Dong, H.P.; Dong, H.K.; Lee, S.; Yoon, B.H.; Jung, W.Y.; Lee, K.T.; Cheong, J.H.; Ryu, J.H. The memory-enhancing effects of Euphoria longan fruit extract in mice. J. Ethnopharmacol. 2010, 128, 160–165. [Google Scholar] [CrossRef]
  31. Lin, Y.; Min, J.; Lai, R.; Wu, Z.; Chen, Y.; Yu, L.; Cheng, C.; Jin, Y.; Tian, Q.; Liu, Q.; et al. Genome-wide sequencing of longan (Dimocarpus longan Lour.) provides insights into molecular basis of its polyphenol-rich characteristics. GigaScience 2017, 6, 1–14. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Jia, T.; Wei, D.; Meng, S.; Allan, A.C.; Zeng, L. Identification of Regulatory Genes Implicated in Continuous Flowering of Longan (Dimocarpus longan L.). PLoS ONE 2014, 9, e114568. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Jue, D.; Sang, X.; Liu, L.; Shu, B.; Wang, Y.; Liu, C.; Wang, Y.; Xie, J.; Shi, S. Comprehensive analysis of the longan transcriptome reveals distinct regulatory programs during the floral transition. BMC Genom. 2019, 20, 126. [Google Scholar] [CrossRef] [PubMed]
  34. Wilkins, M.R.; Gasteiger, E.; Bairoch, A.; Sanchez, J.C.; Williams, K.L.; Appel, R.D.; Hochstrasser, D.F. Protein identification and analysis tools in the ExPASy server. Methods Mol. Biol. 1999, 112, 531–552. [Google Scholar]
  35. Saitou, N.; Nei, M. The neighbor-joining method: A new method for reconstructing phylogenetic trees. Mol. Biol. Evol. 1987, 4, 406–425. [Google Scholar]
  36. Chen, C.; Xia, R.; Chen, H.; He, Y. TBtools, a Toolkit for Biologists integrating various HTS-data handling tools with a user-friendly interface. bioRxiv 2018. [Google Scholar] [CrossRef]
  37. Lescot, M.; Déhais, P.; Thijs, G.; Marchal, K.; Moreau, Y.; van de Peer, Y.; Rouzé, P.; Rombauts, S. PlantCARE, a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences. Nucleic Acids Res. 2002, 30, 325–327. [Google Scholar] [CrossRef]
  38. Wu, J.; Zhang, H.; Liu, L.; Li, W.; Wei, Y.; Shi, S. Validation of Reference Genes for RT-qPCR Studies of Gene Expression in Preharvest and Postharvest Longan Fruits under Different Experimental Conditions. Front. Plant Sci. 2016, 7, 780. [Google Scholar] [CrossRef] [Green Version]
  39. Livak, K.J.; Schmittgen, T.D. Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method. Methods 2001, 25, 402–408. [Google Scholar] [CrossRef]
  40. Su, M.; Liu, Z.; Zhuang, Y. Effects of endogenous hormones in bearing basal shoots of ‘Shuizhang’ longan on floral bud differentiation. J. Trop. Crops 1997, 18, 66–71. [Google Scholar]
  41. Hou, Z.; Huang, W. Immunohistochemical localization of IAA and ABP1 in strawberry shoot apexes during floral induction. Planta 2005, 222, 678–687. [Google Scholar] [CrossRef]
  42. Jenik Pablo, D.; Barton, M.K. Surge and destroy: The role of auxin in plant embryogenesis. Development 2005, 132, 3577–3585. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Leyser, O. The fall and rise of apical dominance. Curr. Opin. Genet. Dev. 2005, 15, 468–471. [Google Scholar] [CrossRef] [PubMed]
  44. Tim, U.; Jane, M.; Gretchen, H.; Guilfoyle Tom, J. Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements. Plant Cell 1997, 9, 1963–1971. [Google Scholar]
  45. Guilfoyle, T.; Hagen, G.; Ulmasov, T.; Murfett, J. How does auxin turn on genes? Plant Physiol. 1998, 118, 341–347. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Piya, S.; Shrestha, S.K.; Binder, B.; Stewart, N.; Hewezi1, T. Protein-protein interaction and gene co-expression maps of ARFs and Aux/IAAs in Arabidopsis. Front. Plant Sci. 2014, 5, 744. [Google Scholar] [CrossRef] [Green Version]
  47. Li, S.; Xie, Z.; Hu, C.; Zhang, J. A Review of Auxin Response Factors (ARFs) in Plants. Front. Plant Sci. 2016, 7, 47. [Google Scholar] [CrossRef] [Green Version]
  48. Tim, U.; Gretchen, H.; Tom, G.J. Dimerization and DNA binding of auxin response factors. Plant J. 1999, 19, 309–319. [Google Scholar]
  49. Mark, R.; Sébastien, P.; Dolf, W. Auxin Response Factors: Output control in auxin biology. J. Exp. Bot. 2018, 69, 179–188. [Google Scholar]
  50. Barbara, M.; Colette, A.H.T.; Xiang, D.; Nerys, W.; González, L.L.; Saiko, Y.; Margo, S.; Raju, D.; Dolf, W. Auxin response cell-autonomously controls ground tissue initiation in the early Arabidopsis embryo. Proc. Natl. Acad. Sci. USA 2017, 114, E2533–E2539. [Google Scholar]
  51. Ding, S.F.; Chen, W.S.; Su, C.; Du, B.S.; Twitchin, B.; Bhaskar, V.K. Changes in free and conjugated indole-3-acetic acid during early stage of flower bud differentiation in Polianthes tuberosa. Plant Physiol. Biochem. 1999, 37, 161–165. [Google Scholar] [CrossRef]
  52. Wang, H.; Zhao, J.; Wang, X.; Shi, X.; Wang, B.; Zheng, X.C.; Liu, F. The Influence of Changes of Endogenous Hormones in Shoot on the Grapes Flower Bud Differentiation in Greenhouse. Scientia Agricultura Sinica 2014, 134, 1065–1071. [Google Scholar]
  53. Yang, Z.; Huang, X.; Chen, Y. Changes of Endogenous Hormone Level during Flower Development in On-season and Off-season Longan. J. Anhui Agric. Sci. 2019, 47, 47–50. [Google Scholar]
  54. Liu, N.; Wu, S.; van Houten, J.; Wang, Y.; Ding, B.; Fei, Z.; Clarke, T.H.; Reed, J.W.; van der Knaap, E. Down-regulation of AUXIN RESPONSE FACTORS 6 and 8 by microRNA 167 leads to floral development defects and female sterility in tomato. J. Exp. Bot. 2014, 65, 2507–2520. [Google Scholar] [CrossRef] [Green Version]
  55. Liu, X.; Dinh, T.T.; Li, D.; Shi, B.; Li, Y.; Cao, X.; Guo, L.; Pan, Y.; Jiao, Y.; Chen, X. AUXIN RESPONSE FACTOR 3 integrates the functions of AGAMOUS and APETALA2 in floral meristem determinacy. Plant J. 2014, 80, 629–641. [Google Scholar] [CrossRef] [Green Version]
  56. Zhang, K.; Wang, R.; Zi, H.; Li, Y.; Cao, X.; Li, D.; Guo, L.; Tong, J.; Pan, Y.; Jiao, Y.; et al. AUXIN RESPONSE FACTOR3 Regulates Floral Meristem Determinacy By Repressing Cytokinin Biosynthesis and Signaling. Plant Cell 2018, 30, 705–2017. [Google Scholar] [CrossRef] [Green Version]
  57. Przemeck, G.K.; Mattsson, J.; Hardtke, C.S.; Sung, Z.R.; Berleth, T. Studies on the role of the Arabidopsis gene MONOPTEROS in vascular development and plant cell axialization. Planta 1996, 200, 229–237. [Google Scholar] [CrossRef]
  58. Fowler, S.; Lee, K.; Onouchi, H.; Samach, A.; Richardson, K.; Morris, B.; Coupland, G.; Putterill, J. GIGANTEA: A circadian clock-controlled gene that regulates photoperiodic flowering in Arabidopsis and encodes a protein with several possible membrane-spanning domains. Embo J. 1999, 18, 4679–4688. [Google Scholar] [CrossRef] [Green Version]
  59. Galvão, V.C.; Collani, S.; Horrer, D.; Schmid, M. Gibberellic acid signaling is required for ambient temperature-mediated induction of flowering in Arabidopsis thaliana. Plant J. 2015, 84, 949–962. [Google Scholar] [CrossRef] [Green Version]
  60. Yamaguchi, N.; Winter, C.M.; Wu, M.; Kanno, Y.; Yamaguchi, A.; Seo, M.; Wagner, D. Gibberellin acts positively then negatively to control onset of flower formation in Arabidopsis. Science 2014, 344, 638–641. [Google Scholar] [CrossRef]
  61. Tomoko, N.; Takamasa, S.; Yumiko, T.; Rie, I.; Tetsuya, H.; Hitoshi, S.; Sumie, I. Jasmonic acid facilitates flower opening and floral organ development through the upregulated expression of SlMYB21 transcription factor in tomato. Biosci. Biotechnol. Biochem. 2018, 82, 292–303. [Google Scholar]
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Figure 1. The location in scaffold of Dimocarpus longan auxin response factor (DlARF) family. The scaffold numbers and size are indicated at the top and bottom of each bar, respectively. The scale is in kilo bases (kb).
Figure 1. The location in scaffold of Dimocarpus longan auxin response factor (DlARF) family. The scaffold numbers and size are indicated at the top and bottom of each bar, respectively. The scale is in kilo bases (kb).
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Figure 2. The phylogenetic analysis of ARF family genes of Arabidopsis, apple, and longan. Tree was constructed via neighbor-joining method with 1000 bootstrap replications.
Figure 2. The phylogenetic analysis of ARF family genes of Arabidopsis, apple, and longan. Tree was constructed via neighbor-joining method with 1000 bootstrap replications.
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Figure 3. Gene structure analysis of DlARFs family genes. The blue boxes, yellow boxes, and the black lines indicate upstream/downstream, exons, and introns, respectively.
Figure 3. Gene structure analysis of DlARFs family genes. The blue boxes, yellow boxes, and the black lines indicate upstream/downstream, exons, and introns, respectively.
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Figure 4. Analysis of conserved domain in DlARFs proteins. All conserved domains were identified by MEME database with the complete amino acid sequences of DlARFs.
Figure 4. Analysis of conserved domain in DlARFs proteins. All conserved domains were identified by MEME database with the complete amino acid sequences of DlARFs.
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Figure 5. Expression analysis of DlARF genes in different tissues of longan.
Figure 5. Expression analysis of DlARF genes in different tissues of longan.
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Figure 6. Expression analysis of DlARF genes from different varieties. (a): expression of DlARFs in apical buds of ‘Shixia’ from November to January of the following year; (b): expression of DlARFs in the buds of the ‘Lidongben’ and ‘Sijimi’. Note: SX is Shixia, SJM is Sijimi, LDB is lidongben.
Figure 6. Expression analysis of DlARF genes from different varieties. (a): expression of DlARFs in apical buds of ‘Shixia’ from November to January of the following year; (b): expression of DlARFs in the buds of the ‘Lidongben’ and ‘Sijimi’. Note: SX is Shixia, SJM is Sijimi, LDB is lidongben.
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Figure 7. Expression patterns of seven DlARF genes during floral bud physiological differentiation of longan. The x-axis indicates months and the y-axis indicates the relative gene expression. Values with the different letter (a, b, c) were significantly different when assessed using Duncan’s multiple range test (p < 0.05).
Figure 7. Expression patterns of seven DlARF genes during floral bud physiological differentiation of longan. The x-axis indicates months and the y-axis indicates the relative gene expression. Values with the different letter (a, b, c) were significantly different when assessed using Duncan’s multiple range test (p < 0.05).
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Figure 8. Expression patterns of DlARF genes under various hormonal stresses. The x-axis indicates various treatments and the y-axis indicates the relative gene expression; (p < 0.05, n = 3). Values with the different letter (a, b, c) were significantly different when assessed using Duncan’s multiple range test (p < 0.05).
Figure 8. Expression patterns of DlARF genes under various hormonal stresses. The x-axis indicates various treatments and the y-axis indicates the relative gene expression; (p < 0.05, n = 3). Values with the different letter (a, b, c) were significantly different when assessed using Duncan’s multiple range test (p < 0.05).
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Table
Table 1. Physical and chemical properties of ARFs in longan.
Table 1. Physical and chemical properties of ARFs in longan.
Gene NameGene IdentifierExon NumbersPIMW (kDa)Genomic PositionORF Length (bp)Homolog in ArabidopsisMR Domain (Amino Acid Content)
DlARF1Dlo.020240.1186.66132.00scaffold41:473073-4813723558AtARF6QSL
DlARF2Dlo.022331.1186.6180.87scaffold48:620922-6260162238AtARF3GLS
DlARF3Dlo.025765.125.7663.54scaffold59:841815-8452591728AtARF10PSV
DlARF4Dlo.030332.1136.8376.01scaffold78:251174-2545492043AtARF11.18LSV
DlARF5Dlo.002610.126.4872.72scaffold113:973236-9758191986AtARF16GLS
DlARF6Dl0.005415.2226.15166.68scaffold139:542989-5503754497AtARF2EPS
DlARF7Dlo.011077.126.5877.10scaffold209:327655-3304502100AtARF16QSL
DlARF8Dlo.011327.1145.89100.03scaffold211:316240-3246252718AtARF6QSL
DlARF9Dlo.013714.2136.10126.04scaffold253:313870-3217813393AtARF19QSL
DlARF10Dlo.014083.1146.0577.38scaffold260:282418-2860132079AtARF9LSV
DlARF11Dlo.016820.1125.9669.86scaffold321:299097-3040131878AtARF1PSV
DlARF12Dlo.019200.4176.22106.61scaffold382:283090-3004322850AtARF8QSL
DlARF13Dlo.023607.1115.99104.31scaffold518:150916-1561842793 LSV
DlARF14Dlo.024143.1128.0370.51scaffold539:226240:2310341902 GLS
DlARF15Dlo.027785.3126.8788.20scaffold661:72501:766202376AtARF2LSV
DlARF16Dlo.029636.1145.27104.34scaffold738:134978:1414462829AtARF5QSL
DlARF17Dlo.032913.147.2179.38scaffold905:165555-1696102181AtARF16GLS
Note: Q, glutamine; S, serine; L, leucine; P, proline; G, glycine; E, glutamic acid; V, Valine.

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Peng, Y.; Fang, T.; Zhang, Y.; Zhang, M.; Zeng, L. Genome-Wide Identification and Expression Analysis of Auxin Response Factor (ARF) Gene Family in Longan (Dimocarpus longan L.). Plants 2020, 9, 221. https://doi.org/10.3390/plants9020221

AMA Style

Peng Y, Fang T, Zhang Y, Zhang M, Zeng L. Genome-Wide Identification and Expression Analysis of Auxin Response Factor (ARF) Gene Family in Longan (Dimocarpus longan L.). Plants. 2020; 9(2):221. https://doi.org/10.3390/plants9020221

Chicago/Turabian Style

Peng, Yuan, Ting Fang, Yiyong Zhang, Mengyuan Zhang, and Lihui Zeng. 2020. "Genome-Wide Identification and Expression Analysis of Auxin Response Factor (ARF) Gene Family in Longan (Dimocarpus longan L.)" Plants 9, no. 2: 221. https://doi.org/10.3390/plants9020221

APA Style

Peng, Y., Fang, T., Zhang, Y., Zhang, M., & Zeng, L. (2020). Genome-Wide Identification and Expression Analysis of Auxin Response Factor (ARF) Gene Family in Longan (Dimocarpus longan L.). Plants, 9(2), 221. https://doi.org/10.3390/plants9020221

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