Ethylene Response Factor MaERF012 Modulates Fruit Ripening by Regulating Chlorophyll Degradation and Softening in Banana

Ethylene response factors (ERFs) are one of largest plant-specific transcription factor families involved in fruit ripening. However, the regulatory mechanism by which ERFs modulate fruit yellowing and softening remains unknown in banana. We previously found that the transcription of MaERF012 was closely related to ‘Fenjiao’ banana fruit ripening. Herein, we found that MaERF012 was differentially expressed in the fruit pulp and peel and was closely related to fruit ripening. MaERF012 activated the promoter activity of one chlorophyll degradation gene (MaSGR1), two starch degradation genes (MaGWD1 and MaAMY3), and three cell wall degradation genes (MaPL8, MaEXP-A8, and MaXYL23-like), which were tested by EMSA, Y1H, and DLR. Transient overexpression of MaERF012 accelerates fruit ripening by promoting fruit yellowing and softening by up-regulating the transcription of chlorophyll, starch, and cell wall degradation genes. Over-expression of MaERF012 alters the transcriptome profiles of the fruit peel and pulp, and the differentially expressed genes were mainly enriched in starch and sucrose metabolism, plant hormone signal transduction, biosynthesis of secondary metabolism, and fructose and mannose metabolism. Overall, the data showed that MaERF012 acts as a transcriptional activator by regulating fruit ripening by activating the transcription of chlorophyll, starch, and cell wall degradation genes.


Introduction
Banana (Musa acuminata L.) fruit ripening is a complicated biochemical and physiological process that causes physical changes including color change (from green to yellow), softening [1], and the appearance of aromatic substances [2]. Chlorophyll (Chl) degradation is a common natural occurrence during the ripening of green to yellow fruit peels [3], which is a multi-step enzymatic process [4]. The mechanism of Chl degradation has been well reported in plants [5]; however, few previous studies have reported the regulation of Chl degradation in fruit. In apple, MdPUB24 modulates ubiquitination of MdBEL7 to accelerate Chl degradation by activating the promoter activity of MdCLH, MdPPH2, and MdRCCR2 [4]. In lychee, LcABF1/2/3 promotes fruit Chl degradation by increasing the expression of LcSGR, LcPAO, LcCLH, and LcNYC [5]. Previous studies on banana have identified many nonfluorescent Chl catabolites (NCCs), fluorescent catabolites (FCCs), and stay-green protein (SGR) genes related to Chl degradation [3,6,7]. Additionally, MaLUL2 inhibited fruit Chl degradation by repressing the transcription of MaNYC1, MaSGR1, MaSGR2, MaPPH, The selected pretreated fruit were split into four groups randomly. Control (natural ripening) and ethephon treatment (1000 nL· L −1 ethephon (ETH) solution for 1 min immersion) groups each contained 180 fingers of bananas, which were divided into 18 subgroups (each with 10 fingers) and stored separately in chambers at 25 • C for ripening. The suitable 1-MCP treatment group (400 nL·L −1 for 1 h (1-MCP400)) and the high-concentration 1-MCP treatment group (3200 nL·L −1 for 1 h (1-MCP3200)) each contained 270 fingers of bananas, which were similarly split into 27 subgroups (each with 10 fingers) and stored separately in chambers at 25 • C. After 5 days of storage, the fruit were treated with 1000 nL·L −1 ethephon (ETH) solution for 1 min immersion and then stored at 25 • C for ripening. This group's fruit were collected at 0 d, 0.25 d (6 h), 1 d, 3 d, and 5 d after storage. Moreover, the 1-MCP400 group was also collected at 1, 3, and 5 d after ethephon treatment and the 1-MCP3200 group was collected at 1, 3, 5, 7, and 9 d after ethephon treatment ( Figure 1). ually separated into individual fingers, and fruit with uniform maturity and without ual defects were selected. The bananas were then dipped in a 0.2% (w/v) hypochlo solution for 10 min and soaked in a 500 µL·L −1 mixture of iprodione (Huifeng, Yangzh China) and prochloraz (Kuaida, Yangzhou, China) for 1 min.
The selected pretreated fruit were split into four groups randomly. Control (nat ripening) and ethephon treatment (1000 nL L −1 ethephon (ETH) solution for 1 min imm sion) groups each contained 180 fingers of bananas, which were divided into 18 subgro (each with 10 fingers) and stored separately in chambers at 25 °C for ripening. The suit 1-MCP treatment group (400 nL L −1 for 1 h (1-MCP400)) and the high-concentratio MCP treatment group (3200 nL L −1 for 1 h (1-MCP3200)) each contained 270 finger bananas, which were similarly split into 27 subgroups (each with 10 fingers) and sto separately in chambers at 25 °C. After 5 days of storage, the fruit were treated with 1 nL L −1 ethephon (ETH) solution for 1 min immersion and then stored at 25 °C for ripen This group's fruit were collected at 0 d, 0.25 d (6 h), 1 d, 3 d, and 5 d after storage. Moreo the 1-MCP400 group was also collected at 1, 3, and 5 d after ethephon treatment and 1-MCP3200 group was collected at 1, 3, 5, 7, and 9 d after ethephon treatment (Figure The color index was evaluated using the fruit ripening index, which was assessed a scale from 1 to 7 as described by Zhu et al. [28]. For ethylene production, three fruit w weighed and individually placed in an airtight container equipped with a rubber top for 2 h at 25 °C, and triplicate samples of 1 mL of headspace gas were taken for ethy production according to the method of Zhu et al. [28]. Fruit and pulp firmness was m ured according to the methods described by Zhu et al. [28]. Fruit firmness (N) was pressed as the mean of three measurements. The color index was evaluated using the fruit ripening index, which was assessed on a scale from 1 to 7 as described by Zhu et al. [28]. For ethylene production, three fruit were weighed and individually placed in an airtight container equipped with a rubber topper for 2 h at 25 • C, and triplicate samples of 1 mL of headspace gas were taken for ethylene production according to the method of Zhu et al. [28]. Fruit and pulp firmness was measured according to the methods described by Zhu et al. [28]. Fruit firmness (N) was expressed as the mean of three measurements.

RNA Extraction and Transcript Analysis
RNA was extracted from 'Fenjiao' banana fruit peels and pulp using an RNA Extraction Kit (Aidlab Biotechnologies Co., Ltd., Beijing, China) and then reversed to cDNA using a Reverse Transcription Kit (Takara, Japan). RT-qPCR was conducted according to Song et al. [12]. The reaction system contained 10 µL of SYBR Premix Ex Taq, 1 µL of upstream and 1 µL of downstream primers, 100 ng of cDNA, and a volume of sterile deionized water leading to a final volume of 20 µL. The same set of reaction conditions was for all primers: 95 • C for 30 s, followed by 40 cycles at 95 • C for 5 s, 60 • C for 15 s, and finally 72 • C for 20 s. The expression levels of genes on day 0 were set as the calibrator. MaACTIN was set as the reference gene for the expression assay [29].

Subcellular Localization
Subcellular location was analyzed according to Ding et al. [30]. The full coding sequence (CDS) of MaERF012, excluding the stop codon, was inserted into the pEAQ-GFP vector, which was stored in our laboratory, and a pEAQ-GFP vector with no insert was used as the control. The MaERF012-pEAQ-GFP and pEAQ-GFP vectors were separately transformed in the Agrobacterium tumefaciens strain GV3101, and the MaERF012-pEAQ-GFP and pEAQ-GFP vectors were then allowed to separately infiltrate into N. benthamiana leaves. After 36 h of infiltration, the subcellular location was detected using a universal fluorescence microscope (Zeiss Axioskop 2 Plus, Zeiss, Oberkochen, Germany). All transient expression assays were repeated at least three times.

Dual-Luciferase Transient Expression (DLR) Assays
ERF TFs regulate download target genes by binding the GCC-box motif in their promoters [31]. Several Chl, cell wall, and starch degradation genes were identified in our previous work, and we found that the promoter sequence of four Chl degradationrelated genes (MaSGR1, MaNYC, MaPPH, and MaNOL), four cell wall degradation-related genes (MaPL8, MaEXP-A8, MaSUR14-like, and MaXYL23-like), and three starch degradationrelated genes (MaBAM3, MaGWD1, and MaAMY3) contained the GCC-box motif. These genes were individually transformed into the pGreenII 0800-LUC vector as a reporter, and the CDS of MaERF012 was transformed into the pGreenII 62-SK vector as an effector. The pGreenII 0800-LUC and pGreenII 62-SK vectors were stored in our laboratory. The effector and reporter plasmids were co-infiltrated into N. benthamiana leaves. After 48 h of infiltration, DLR was detected according to the method of Song et al. [12]. Briefly, a DLR Assay kit (Promega, Madison, WI, USA) was used, and at least six independent replicates were conducted for each combination.

Yeast One-Hybrid (Y1H) Assay
Y1H assays were carried out using the Matchmaker Gold Yeast One-Hybrid System (Clontech, Fitchburg, WI, USA). The promoters of MaSGR1, MaGWD1, MaAMY3, MaPL8, MaEXP-A8, and MaXYL23-like were cloned into pAbAi, which was stored in our laboratory. It was then linearized and separately introduced into the Y1H Gold strain. The CDS of MaERF012 was ligated to the pGADT7 vector and subsequently introduced into the yeast strain. It was then transferred into the aforementioned bait reporter yeast strain containing the promoters of MaSGR1, MaGWD1, MaAMY3, MaPL8, MAEXP-A8, and MaXYL23-like. Their interaction was tested according to the method of Song et al. [12].

Electrophoretic Mobility Shift Assay (EMSA)
The CDS of MaERF012, excluding the stop codon, was cloned into the pGEX-4T-1 vector (which was stored in our laboratory) to obtain the GST-MaERF012 recombinant plasmid and was then transformed into BM Rosetta (DE3) cells following the method of Song et al. (2022). The GST-MaERF012 protein was induced by 0.5 mM isopropyl-β-Dthiogalactopyranoside (IPTG) (Car. no. 9030; TaKaRa, Tokyo, Japan) at 28 • C for 6 h and purified using a GST Purification Kit (Cat. No. 635619, Clontech, Takara, Dalian, China) according to the manufacturer's protocol.
The probes that contained the GCC-box (GCCGCC/GGCGGC) sequence derived from the promoters of the Chl degradation-related gene (MaSGR1), two starch degradationrelated genes (MaGWD1 and MaAMY3), and three cell wall degradation genes (MaPL8, MaEXP-A8, and MaXYL23-like) were labeled with biotin using the PierceTM Biotin 3 End The CDS of MaERF012 was cloned into the pMDC32 vector, which was stored in our laboratory. The 'Fenjiao' banana fruits were then infected as described previously [9]. The fruits were stored at 22 • C and relative humidity was set at 90%. The ethylene production, color index, firmness, and transcript level were tested and collected according to methods described above.
The empty vector and OE-MaERF012 banana fruit pulp and peel samples collected on day 3 were further investigated via RNA-Seq analysis using an Illumina HiSeq platform. Triple biological replicates were used for each sampling time point. Clustered profiles with a fold-change of ≥2 and a p-value ≤ 0.05 were considered to be differentially expressed genes (DEGs). A heat map was drawn using TBtools [32].

Data Analysis
All experiments were conducted in triplicate or six times in a completely randomized design. The results are presented as the mean ± SD using three or six independent biological replicates; statistical significance was analyzed with ANOVA followed by Duncan's multiple range test using SPSS version 16.0 (SPSS, Inc., Chicago, IL, USA). Charts were created using SigmaPlot 12.0 (Systat Software Inc., San Jose, CA, USA). All primers used in the present study are listed in Table S1.

Characterization of MaERF012
As shown in Figure 1, different 1-MCP treatments were employed in the present study, of which suitable 1-MCP treatment inhibited fruit ripening, while a high concentration of 1-MCP caused a ripening disorder in 'Fenjiao' banana fruits, as described in a previous study [3]. The transcript level of MaERF012 increased with fruit ripening, but 1-MCP treatment significantly repressed its expression in 'Fenjiao' banana pulp and peel during storage. In the peel and pulp, the transcription of MaERF012 in the suitable 1-MCP treatment could recover from ethephon treatment after 5 days of storage. However, in the high-concentration 1-MCP treatment, the expression of MaERF012 could recover from ethephon treatment in the pulp but not in the peel after 5 days of storage ( Figure 2A), which was similar to our previous study [3].
As shown in Figure S1, we found that MaERF012 protein contained 188 amino acids and an AP2/ERF domain. To understand which group MaERF012 belongs to, tomato, papaya, and other banana ERF proteins were used for phylogenetic analysis. As shown in Figure S2, MaERF012 was closely related to SlERF014. Additionally, we found that MaERF012 was located in the cell nucleus ( Figure 2B).

MaERF012 Activates the Transcription Activity of Chl, Starch, and Cell Wall Degradation Genes
The promoter fragments of four Chl degradation-related genes (MaSGR1, MaNYC, MaPPH, and MaNOL), three starch degradation-related genes (MaBAM3, MaGWD1, and MaAMY3) and four cell wall degradation-related genes (MaEXP-A8, MaPL8, MaSUR14-like, and MaXYL23-like) containing the GCC-box motif were cloned to the reporter vector, and the CDS of MaERF012 was inserted into the MaERF012-SK effector vector ( Figures S3 and S4). As shown in Figure 3A, the LUC activity of MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like was significantly higher (2-3 fold) in the presence of MaERF012 compared to the control group; however, the LUC activity of MaNYC, MaPPH, MaNOL, MaBMY3, and MaSUR14-like in the presence of MaERF012 was not significantly different compared to the control. These data indicate that MaERF012 enhanced the promoter activity of MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like, while MaERF012 had no effect on the promoter activities of MaNYC, MaPPH, MaNOL, MaBMY3, and MaSUR14-like [3]. The promoter fragment of MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like was then inserted into pAbAi and introduced into the Y1H Gold strain to detect the basal activity of MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like. No basal activity was found for the MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like promoters in yeast ( Figure 3B). AD-MaERF012 was transformed into the Y1H reporter strain, and the MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like promoter grew well in the presence of AbA, suggesting that MaERF012 could bind to the promoter of MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like ( Figure 3B). Moreover, an EMSA was performed to verify the interaction. The GST-MaERF012 protein was obtained as shown in Figure S5, which was used for the EMSA assay. The findings indicate that MaERF012 interacts with the promoter fragment of MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like. In addition, MaERF012 cannot bind to the promoter fragment when GGCGGC mutates to AAAAAA ( Figure 4). As shown in Figure S1, we found that MaERF012 protein contained 188 amino acids and an AP2/ERF domain. To understand which group MaERF012 belongs to, tomato, papaya, and other banana ERF proteins were used for phylogenetic analysis. As shown in Figure S2, MaERF012 was closely related to SlERF014. Additionally, we found that MaERF012 was located in the cell nucleus ( Figure 2B).

Overexpression of MaERF012 Promotes 'Fenjiao' Banana Ripening
To further verify whether MaERF012 mediates fruit ripening by modulating Chl, cell wall, and starch degradation, transient overexpression of MaERF012 was performed in 'Fenjiao' banana. As shown in Figure 5A, the overexpression of MaERF012 significantly increased the transcript level of MaERF012, which suggests that an MaERF012-overexpressing (OE) line was successfully created for 'Fenjiao' banana. The overexpression of MaERF012 markedly promotes fruit peel coloring from green to yellow and accelerates fruit softening, ethylene production, and color change compared to the empty vector control ( Figure 5B-F). The expression of MaSGR1 in 'Fenjiao' banana peel and the transcription of MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like in 'Fenjiao' banana pulp was significantly induced in MaERF012-overexpressing lines compared to the control ( Figure 5G).  Figure 3B). Moreover, an EMSA was performed to verify the interaction. The GST-MaERF012 protein was obtained as shown in Figure S5, which was used for the EMSA assay. The findings indicate that MaERF012 interacts with the promoter fragment of MaSGR1, MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like. In addition, MaERF012 cannot bind to the promoter fragment when GGCGGC mutates to AAAAAA (Figure 4).    pressing (OE) line was successfully created for 'Fenjiao' banana. The overexpression of MaERF012 markedly promotes fruit peel coloring from green to yellow and accelerates fruit softening, ethylene production, and color change compared to the empty vector control ( Figure 5B-F). The expression of MaSGR1 in 'Fenjiao' banana peel and the transcription of MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like in 'Fenjiao' banana pulp was significantly induced in MaERF012-overexpressing lines compared to the control ( Figure 5G).

Transcriptomic Analysis of MaERF012 Overexpression in 'Fenjiao' Banana
As shown in Figure 5, the overexpression of MaERF012 significantly promotes fruit ripening. To obtain a global overview of the expression changes in MaERF012-overexpressing fruits, we analyzed the DEGs across MaERF012-overexpressing and control lines with RNA-Seq. Figure 6A shows that 2151 DEGs were identified in MaERF012-overexpressing and control lines in 'Fenjiao' banana peel, including 814 up-regulated genes and 1337 downregulated genes. Among the top 30 enriched metabolic pathways, the DEGs were most enriched in metabolic pathways, biosynthesis of secondary metabolites, phenylpropanoid biosynthesis, flavonoid biosynthesis, starch and sucrose metabolism, and plant hormone signal transduction ( Figure 6B). We further analyzed the expression profiles and signaling pathway of ethylene synthesis, the ABA signaling pathway, and Chl, cell wall, and starch degradation-related genes. As shown in Figure 7, the overexpression of MaERF012 induced the transcription of most genes associated with ethylene synthesis and its signaling pathway, the ABA signaling pathway, and Chl, cell wall, and starch degradation in 'Fenjiao' banana peel. Specifically, MaACS, MaACO, MaEBF1, and MaERF4-like had increased transcription in ethylene synthesis and the signaling pathway. MaPYL4-like and MaABI5-like showed increased transcription in the ABA signaling pathway. MaSGR1 and MaPPH showed increased transcription in Chl degradation. MaBAM3 and MaAMY3 had increased transcription in the starch signaling pathway, and MaEXP-A8, MaPL8, and MaXYL23 had increased transcription in cell wall degradation.   Moreover, as shown in Figure 8A, 4977 DEGs were identified across MaERF012-ove expressing and control lines in 'Fenjiao' banana pulp, including 1663 up-regulated gene Moreover, as shown in Figure 8A, 4977 DEGs were identified across MaERF012overexpressing and control lines in 'Fenjiao' banana pulp, including 1663 up-regulated genes and 3314 down-regulated genes. Among the top 30 metabolic pathways, the DEGs were most enriched in the biosynthesis of secondary metabolites, the biosynthesis of antibiotics, the biosynthesis of amino acids, starch and sucrose metabolism, plant hormone signal transduction, and fructose and mannose metabolism pathways ( Figure 8B). The expression profiles of ethylene synthesis and the signaling pathway, the ABA signaling pathway, and cell wall and starch degradation-related genes were also analyzed in 'Fenjiao' banana pulp. As shown in Figure 9, the overexpression of MaERF012 induced the transcription of most genes associated with ethylene synthesis and signaling, ABA signaling, and starch and cell wall degradation. Specifically, MaACS3, MaACO, and MaEBF1 in ethylene synthesis and its signaling pathway showed up-regulation. MaPYL8-like and MaABI5-like were up-regulated in the ABA signaling pathway. MaBAM1 and MaAMY2 showed increased expression in the starch signaling pathway. MaEXP-A8, MaPL8, and MaXYL23 had increased expression in cell wall degradation. However, the expression of MaGWD1 was repressed in RNA-Seq data.

Discussion
Yellowing and softening are two vital indicators of banana fruit ripening, which are co-determined due to Chl, cell wall, and starch degradation [6,9]. 'Fenjiao' banana fruit accumulates an abundance of starch in the cell wall to maintain banana firmness, and the fruit was harvested at an 85-90% maturity stage in terms of green peel [9,27]. During fruit ripening, yellowing correlates with Chl degradation [5], and softening is closely associated with starch and cell wall degradation [9]. 'Fenjiao' bananas are a climacteric fruit, ripening quickly due to peak ethylene production after harvesting [12]. Treatments involving 1-MCP have been widely used in flowers, vegetables, and fruits to prolong shelf-life [33,34]. Our previous study found that the use of a low-concentration 1-MCP treatment effectively prolongs storage time for fruit, allowing fruit to ripen normally after ethephon treatment. However, the use of a high concentration of 1-MCP caused a ripening disorder (fruit pulp can soften but the peel does not turn yellow), even after treatment with ethephon [3].
The ERF TF family, a downstream component of the ethylene signaling pathway, has been reported to modulate plant growth, stress response, and fruit development and ripening [17,35]. However, the mechanisms by which most ERFs modulate climacteric fruit ripening are still unknown. Herein, we demonstrated that the expression of MaERF012 was induced with fruit ripening and inhibited by 1-MCP treatment (suitable and unsuitable treatment). However, the expression of MaERF012 could recover under suitable 1-MCP treatment followed by ethephon treatment in both the pulp and peel. Under the highconcentration 1-MCP treatment, the expression of MaERF012 in fruit peel did not recover following ethephon treatment (Figure 2). The uneven expression of MaERF012 in fruit peel and pulp may be due to a fruit ripening disorder partially induced by high-concentration 1-MCP treatment. The results indicate that MaERF012 may modulate a fruit ripening disorder caused by the high-concentration 1-MCP treatment, which is consistent with our previous work [3].
Several ERFs have been shown to be involved in Chl degradation. PyERF3 interacts with PybHLH3 and PyMYB114 proteins to form protein complexes that mediate red coloration in pear fruit [36]. In citrus, CitERF13 and CitERF6 modulate Chl degradation in fruit by directly activating the transcription of CitPPH [37,38]. In lemon, ClERF114 may regulate fruit Chl degradation by modulating ClNCED5, ClPPH, and ClCLH1 [39]. In tomato, SlERF16 promotes fruit degreening by activating the transcription of SlPPH genes [38]. The reduced expression of SlERF.F12 represses tomato fruit ripening and color changes [40]. Four Chl degradation genes (MaPPH1, MaNCY1, MaNOL, and MaSGR1) were previously identified and found to be closely associated with a fruit ripening disorder caused by high-concentration 1-MCP treatment [3]. Herein, we found that the promoters of MaPPH1, MaNCY1, MaNOL, and MaSGR1 contained a GCC-box, which may be modulated by ERFs. In addition, MaERF012 can directly interact with the MaSGR1 promoter by binding the GCC-box motif. Additionally, the promoter activity of MaSGR1 was induced by MaERF012 (Figures 3 and 4). The high-concentration 1-MCP treatment severely inhibited the transcription of MaERF012, and the transcription of MaERF012 could not recover after ethephon treatment in the peel, which may be the main cause of abnormal yellowing in 'Fenjiao' bananas.
Several studies have previously indicated that ERF TFs also regulate fruit softening by modulating starch and cell wall degradation. In kiwifruit, AdERF9 represses the transcription level of the cell wall degradation gene AdXET5 during fruit ripening [41]. PpeERF2 inhibited cell wall degradation by inhibiting the transcriptional activation activity of PpePG1 in peach [26]. In papaya, CpERF9 modulates cell wall degradation by inhibiting the promoter activity of CpPG5 and CpPME1/2 [20]. In tomato, the overexpression of SlERF.B3 represses the onset of ripening, improves ethylene production, and promotes fruit softening [17,18]; SlERF.F12 represses the expression of SlPG2a and SlPL by directly interacting with their promoter sequence in banana [39]. Additionally MaERF9 modulates fruit softening by regulating eight cell wall degradation-related genes (MaPL2, MaPME3, MaPG1, MaEXP1/2/3/5, and MaXET7) [42]. Our previous work identified three starch and four cell wall degradation genes [3] that contain a GCC-box motif in their promoter sequence. The present study found that MaERF012 can directly bind to the GCC-box motif in the promoters of MaGWD1, MaAMY3, MaEXP-A8, MaPL8, and MaXYL23-like. The promoter activity of these genes was induced by MaERF012 (Figures 3 and 4). Although the high-concentration 1-MCP treatment markedly inhibited the transcription of MaERF012 in pulp, the transcription of MaERF012 was able to recover after ethephon treatment; thus, the expression level of genes associated with starch and cell wall degradation were able to recover to a normal level, allowing the pulp of 'Fenjiao' banana to normally soften. These results support that MaERF012 is involved in modulating the fruit softening process.
Additionally The overexpression of MaERF012 alters the transcriptome profiles of the fruit peel and pulp, and the DEGs were mainly enriched in the biosynthesis of secondary metabolism, fructose and mannose metabolism, starch and sucrose metabolism, and plant hormone signal transduction. Taken together, our data showed that MaERF012 acts as a transcriptional activator and regulates fruit ripening by activating the transcription of Chl, starch, and cell wall degradation genes. These data further indicated that MaERF012 modulates fruit degreening and softening, hence playing a role in the ripening of 'Fenjiao' banana.

Conclusions
Overall, this study identified MaERF012 as a new transcriptional activator with the role of activating the transcriptional activity of genes associated with Chl, starch, and cell wall degradation by directly interacting with their promoters. Moreover, transient overexpression of MaERF012 promotes the ripening of fruit by promoting Chl, starch, and cell wall degradation in fruit. However, under the high-concentration 1-MCP treatment, the expression of MaERF012 was significantly repressed, which then markedly repressed the expression of genes related to Chl, starch, and cell wall degradation that are regulated by MaERF012. The high-concentration 1-MCP treatment caused an uneven expression of MaERF012 in fruit peel and pulp after ethephon treatment, which significantly inhibited the transcription of MaERF012 in the peel and pulp; the transcription of MaERF012 was able to recover after ethephon treatment in the pulp but not in the peel (Figure 10). This uneven expression of MaERF012 affected the degreening and fruit softening process and caused a ripening disorder in 'Fenjiao' banana. Together, our results revealed that the transcriptional regulatory network of MaERF012 is involved in Chl, starch, and cell wall degradation during fruit ripening in 'Fenjiao' banana.
Foods 2022, 11, x FOR PEER REVIEW 18 of 20 expression of MaERF012 was significantly repressed, which then markedly repressed the expression of genes related to Chl, starch, and cell wall degradation that are regulated by MaERF012. The high-concentration 1-MCP treatment caused an uneven expression of MaERF012 in fruit peel and pulp after ethephon treatment, which significantly inhibited the transcription of MaERF012 in the peel and pulp; the transcription of MaERF012 was able to recover after ethephon treatment in the pulp but not in the peel ( Figure 10). This uneven expression of MaERF012 affected the degreening and fruit softening process and caused a ripening disorder in 'Fenjiao' banana. Together, our results revealed that the transcriptional regulatory network of MaERF012 is involved in Chl, starch, and cell wall degradation during fruit ripening in 'Fenjiao' banana. Supplementary Materials: The following supporting information can be downloaded at: www.mdpi.com/xxx/s1, Figure S1. Multiple alignment of MaERF012 (XM_009415777.2) protein with other ERF proteins, Figure S2. Phylogenetic analysis of MaERF012 and other ERF proteins, Figure S3. Picture of the effector and reporter vectors, Figure S4. The location of GCC-box motifs in the promoters of three Chl degradation, three starch, and four cell wall degradation genes, Figure  S5. The recombinant proteins of GST-MaERF012 were tested by gel-stained SDS-PAGE, Table S1. Primers used in the present study. Data Availability Statement: The date are available from the corresponding author.

Conflicts of Interest:
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/foods11233882/s1, Figure S1. Multiple alignment of MaERF012 (XM_009415777.2) protein with other ERF proteins, Figure S2. Phylogenetic analysis of MaERF012 and other ERF proteins, Figure S3. Picture of the effector and reporter vectors, Figure S4. The location of GCC-box motifs in the promoters of three Chl degradation, three starch, and four cell wall degradation genes, Figure S5. The recombinant proteins of GST-MaERF012 were tested by gel-stained SDS-PAGE, Table S1. Primers used in the present study. Data Availability Statement: The date are available from the corresponding author.

Conflicts of Interest:
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.