IPA1 Negatively Regulates Early Rice Seedling Development by Interfering with Starch Metabolism via the GA and WRKY Pathways

Abstract

Ideal Plant Architecture 1 (IPA1) encodes SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 14 (SPL14) with a pleiotropic effect on regulating rice development and biotic stress responses. To investigate the role of IPA1 in early seedling development, we developed a pair of IPA1/ipal-NILs and found that seed germination and early seedling growth were retarded in the ipa1-NIL. Analysis of the soluble sugar content, activity of amylase, and expression of the α-amylase genes revealed that the starch metabolism was weakened in the ipa1-NIL germinating seeds. Additionally, the content of bioactive gibberellin (GA) was significantly lower than that in the IPA1-NIL seeds at 48 h of imbibition. Meanwhile, the expression of GA synthesis-related gene OsGA20ox1 was downregulated, whereas the expression of GA inactivation-related genes was upregulated in ipa1-NIL seeds. In addition, the expression of OsWRKY51 and OsWRKY71 was significantly upregulated in ipa1-NIL seeds. Using transient dual-luciferase and yeast one-hybrid assays, IPA1 was found to directly activate the expression of OsWRKY51 and OsWRKY71, which would interfere with the binding affinity of GA-induced transcription factor OsGAMYB to inhibit the expression of α-amylase genes. In summary, our results suggest that IPA1 negatively regulates seed germination and early seedling growth by interfering with starch metabolism via the GA and WRKY pathways.

1. Introduction

Seed germination is a complex and diverse process that plays an important role in ensuring the continuity of life. Generally, germination starts with water uptake and the reactivation of diverse metabolism processes in the quiescent seed, followed by emergence of the radical and coleoptile [1]. In rice, many nutrients accumulate in the endosperm during seed maturation. As germination progresses, these reserves are hydrolyzed into metabolizable nutrients by a series of hydrolases, then absorbed by the scutellum epithelium and transported to the embryonic axis [2,3]. Thus, the efficient degradation and utilization of seed reserves are particularly important to seed germination and early seedling development.

Starch is the major reserve in rice seed that provides a major carbon source for generating energy and metabolites. During seed germination and early seedling growth, starch is degraded by the concerted action of various hydrolases, including α-amylase, β-amylase, debranching enzyme, and α-glucosidase [4]. Among them, α-amylase is the most abundant hydrolase in rice. It catalyzes the hydrolysis of α-1,4-glucosidic bonds of starch at random sites to generate α-glucose and α-maltose [5,6]. After seed imbibition, α-amylase is synthesized in the aleurone layer and scutellum to break down starch granules. Generally, the expression of rice α-amylase gene αAmys (also called RAmys) is positively and negatively regulated by gibberellin and sugar, respectively [7,8]. After imbibition, GA induces the expression of OsGAMYB (also called MYBGA), which directly binds to the GA response element (GARE) and activates the expression of αAmys [9,10]. Meanwhile, the expression of αAmys is strongly induced by sugar starvation and repressed by various sugars produced during mobilization of endosperm stores [7,11,12]. These results show the complicated regulatory mechanisms of α-amylase.

The GA contents in germinating seeds are determined by GA biosynthesis and metabolism. In brief, GA biosynthesis is catalyzed by the combined actions of ent-copalyl diphosphate synthase (CPS), ent-kaurene synthase (KS), ent-kaurene oxidase (KO), ent-kaurene acid oxidase (KAO), GA 20-oxidase (GA20ox), and GA 3-oxidase (GA3ox), whereas it is inactivated by GA 2-oxidase (GA2ox) [13,14]. The endogenous bioactive GA contents and seed germination rates are correlated with the expression levels of these enzyme-related genes. In a germination-defactive1 (gd1) mutant, the expressions of GA biosynthesis-associated genes OsGA20ox1, OsGA20ox2, and OsGA3ox2 were suppressed, while the expression of the GA inactivation gene OsGA2ox3 was dramatically upregulated, resulting in decreased endogenous GA₄ content and the inhibition of seed germination [15]. Meanwhile, the GA content was significantly lower in the germinating seed embryo of an OsGA20ox2 loss-of-function mutant, which resulted in a delayed seed germination [16].

In Arabidopsis and rice, changes in the expression level of miR156 affect seed dormancy [17,18]. As a target of miR156, the Ideal Plant Architecture 1 (IPA1), which encodes a transcription factor OsSPL14, a member of the SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) family in rice, is an important regulator of plant development [19,20,21]. In ipa1 mutant plants, one nucleotide substitution located in the miR156 recognition site perturbs the miR156-regulated degradation of IPA1 mRNA, leading to an ideal plant architecture with reduced tiller number, increased lodging resistance and panicle branches and, thus, an increase in yield [19,20]. In addition, IPA1 was also identified as a vital regulator to participate in biotic stress response [22,23]. Here, with a pair of IPA1/ipa1-NILs developed in our laboratory, we found that IPA1 negatively regulates the processes of seed germination and early seedling growth. To elucidate the mechanism, we examined the amylase activity, GA content, and expression of the related genes in the NILs. Meanwhile, the relationship between IPA1 and two transcriptional repressors (WRKY51 and WRKY71) was investigated, respectively. Our work suggests that the elevated levels of IPA1 expression retards seed germination and early seedling growth through GA and WRKY pathways. These findings provide new insight into understanding the function of IPA1 in seedling development.

2. Results

2.1. ipa1 Retards Seed Germination and Early Seedling Growth of Rice

To investigate the role of the IPA1 gene in rice seedling development, we developed a pair of IPA1/ipa1-NILs and compared the expression pattern of IPA1 in germinating seeds. We found that IPA1 expression was significantly higher in the ipa1-NIL seeds after 24 h imbibition compared with the IPA1-NIL seeds (Figure 1A). In a germination experiment, the initiation time of seed sprouting was delayed by approximately 12 h compared to that of the IPA1-NIL seeds (Figure 1B). Meanwhile, the percentage of germinated ipa1-NIL seeds was significantly decreased from 36 to 96 h after the initial imbibition (Figure 1B). Additionally, the plateau values of seed germination peaked later for ipa1-NIL, although no significant difference was found in germination percentage after 108 h (Figure 1B). Moreover, with the dehulled seeds of NILs, we found that the shoot was significantly decreased in the ipa1-NIL seeds at 48 h after initial imbibition (Figure 1C). Then, the root and shoot lengths were recorded for intact seeds. At 96 h after germination in Petri dishes, the shoot length was decreased by 22.66% and the root length was decreased by 24.53% in the ipa1-NIL seedlings compared with those of the IPA1-NIL seedlings (Figure 1D). Overall, these results indicate that IPA1 participates in seed germination and early seedling growth in rice and that ipa1 could retard these processes.

2.2. IPA1 Negatively Regulates Starch Metabolism during Seed Germination and Early Seedling Growth

Sugar is a direct source of energy for seedling vigor. To investigate whether IPA1 regulates seed germination and early seedling growth by modulating sugar accumulation, the sugar content was detected in IPA1/ipa1-NILs. We found that the soluble sugar content of the ipa1-NIL seeds was decreased by 11.63%, 19.05%, and 6.80% after 12, 48, and 96 h imbibition, in the embryo, respectively (Figure 2A), while no significant difference between the NILs was found in the endosperm except for 96 h after initial imbibition (Figure 2A). Amylase is a major enzyme involved in the hydrolysis of starch to soluble sugar during seed germination and seedling growth. At 12 and 48 h of imbibition, the total amylase activity in ipa1-NIL seeds was decreased by 40% and 23.08%, respectively, with the α-amylase activity decreasing by 73.67% and 16.67%, respectively (Figure 2B). Then, the transcript levels of genes encoding α-amylases were measured. The expression of RAmy1A and RAmy1C was significantly lower in ipa1-NIL seeds at 12–24 h of imbibition (Figure 2C,D). Meanwhile, at 12 h of imbibition, RAmy3B/C, RAmy3D, and RAmy3E were significantly downregulated in the ipa1-NIL seeds (Figure 2E–G). It has been reported that the RAmy3 subfamily of genes, especially RAmy3D, are induced by sugar starvation during germination and early seedling growth [24,25]. In the present study, the expression of RAmy3D was induced quickly in the ipa1-NIL seeds, and the levels of RAmy3D were 2.16-, 2.63-, and 5.21-fold higher compared to that in the IPA1-NIL seeds at 24, 36, and 48 h after imbibition, respectively (Figure 2F). Similarly, RAmy3B/C and RAmy3E were also upregulated in the ipa1-NIL seeds at 48 h after imbibition (Figure 2E,G). Additionally, two sucrose transporter genes OsSUT1 and OsSUT4 were found to be downregulated by 62.72% and 54.86% in ipa1-NIL, respectively, at 12 h of imbibition, and then they were induced to be upregulated (Figure 2H,I), the same as to that of RAmy3D. Taken together, these results suggest that IPA1 negatively regulates starch metabolism during germination and early seedling growth.

2.3. The Retarding Effect of Seed Germination and Early Seeding Growth in the ipa1-NIL Seeds Caused by GA Defect

In germinating grains, bioactive GAs are synthesized in the embryo and transported to the aleurone layer to trigger αAmys expression [26]. In our study, the total contents of the bioactive GAs were markedly decreased in the ipa1-NIL seeds at 48 h of imbibition (Figure 3A). Among them, the contents of GA₃, GA₄, and GA₇ were decreased by 22.86%, 11.90%, and 56.18%, respectively (Figure 3A). It has been reported that GAs could induce the expression of OsGAMYB, thereby upregulating the expression of the α-amylase genes [25]. In the present study, the expression of OsGAMYB was downregulated significantly in ipa1-NIL seeds during germination (Figure 3B). Meanwhile, when exogenous GA₃ was applied, the germination rate of the ipa1-NIL seeds was markedly accelerated (Figure 3C–E), and the shoot and root lengths of the ipa1-NIL seeds were significantly increased after 96 h germinated on filter paper soaked with GA₃ solution (Figure 3F,G). These data suggest that ipa1 retards the seed germination and early seedling growth at least via a mechanism mediated by a reduction in the abundance of bioactive GAs.

2.4. Enhanced GA Deactivation in the ipa1-NIL

Bioactive gibberellins are regulated by changes in biosynthetic and deactivation processes. To investigate how the bioactive GAs were decreased in the ipa1-NIL seeds, the expression of GA biosynthetic and inactivated genes was analyzed in the NILs (Figure 4). OsGA20ox1, a representative gene in the third step of GA biosynthesis, was significantly downregulated in the ipa1-NIL during 12–36 h of seed imbibition (Figure 4C), although no significant difference was observed in the expression levels of the GA synthesis-related genes OsCPS1, OsKAO and OsGA20ox2 between the NILs except for OsKAO at the point of 36 h (Figure 4A,B,D). The GA2ox enzymes are involved in GA deactivation in rice. In this study, the OsGA2ox3, OsGA2ox6, and OsGA2ox8 were upregulated in ipa1-NIL during almost the entire imbibition period (Figure 4E,G), and OsGA2ox9 also showed a higher expression level in ipa1-NIL after 36 h, although it was downregulated in the beginning (Figure 4H). Overall, elevated expression of IPA1 enhanced the deactivation process of GAs during seed germination and early seedling growth.

2.5. IPA1 Directly Binds to OsWRKY51 and OsWRKY71 and Promotes Their Expression

Previous studies have demonstrated that OsWRKY51 and OsWRKY71 could suppress the GA-induced expression of α-amylase genes by interfering with the transactivator OsGAMYB [27], and IPA1 was found to be enriched in the OsWRKY51 promoter [28]. In this study, we found that the expression levels of OsWRKY51 and OsWRKY71 in ipa1-NIL seeds were significantly upregulated after 24 h imbibition (Figure 5A,B). By transient dual-luciferase (LUC) assays with rice protoplasts, we found that IPA1 promoted expression of the luciferase reporter gene driven by the OsWRKY51 and OsWRKY71 promoter, respectively (Figure 5C,D). As a transcription factor, IPA1 could regulate the expression of its target genes by binding to the core motif GTAC and/or TGGGCC/T in promoters [28]. Then, we conducted sequence analyses and identified four and eight GTAC motifs in the OsWRKY51 and OsWRKY71 promoter, respectively (Figure 5E,F). Yeast one-hybrid (Y1H) assays were performed to evaluate if IPA1 directly binds to the promoters of OsWRKY51 and OsWRKY71. The cells co-transformed with bait and the prey vectors could grew well on SD/−Leu/−Ura/AbAi plates (Figure 5E,F), indicating that IPA1 can directly bind to the promoters of OsWRKY51 and OsWRKY71. Taking these results together, we conclude that OsWRKY51 and OsWRKY71 are the direct target genes of IPA1.

3. Discussion

IPA1/OsSPL14 is a pleiotropic gene that plays an intricate role in rice plant development and stress response [19,23,29]. In ipa1 plants, a point mutation in the miR156 recognition site perturbed the miR156-regulated degradation of IPA1 mRNA, leading to changed plant architecture [19]. Previous studies have reported that the overexpression of IPA1 or knockout of miR156 enhances seed dormancy [18,22]. Here, we found that the expression level of IPA1 was rapidly upregulated in the soaked ipa1-NIL seeds (Figure 1A). Based on the seed germination rate as well as shoot and root lengths of NILs (Figure 1B–D), our study suggested that the higher expression level of IPA1 in ipa1-NIL delayed seed germination and retarded early seedling growth.

Seed germination and embryo growth rely on the energy supplied by starch decomposition. In the endosperm, starch is decomposed into soluble sugars that are transported into the germinating embryo axis [11,30]. In addition, the enzyme α-amylase is responsible for the degradation of reserve carbohydrate to soluble sugars [31]. In the embryo, soluble sugars provide substrates and energy for fueling embryonic development. In the present study, a lower soluble sugar content was found in the ipa1-NIL embryo (Figure 2A). Further analyses found that the activity of α-amylase was significantly decreased in ipa1-NIL seeds (Figure 2B). Therefore, the delayed germination and retarded early seedling growth in ipa1-NIL seeds could be caused by the suppression of starch metabolism.

It has been reported that GA plays a critical role in promoting seed germination [1]. In plants, GA₁, GA₃, GA₄, and GA₇ are the major bioactive GA forms [13]. Our results revealed that the contents of GA₃, GA₄, and GA₇ were dramatically decreased in ipa1-NIL compared with those in the IPA1-NIL seeds (Figure 3A). These findings are consistent with a previous study which showed that the content of GA₃ and GA₇ was decreased in the fresh seeds of the miR156 mutant [18]. Therefore, we further investigated the effect of exogenous GA on the seed germination of the NILs and, as a result, GA₃-promoted germination and seedling growth were clearly observed in ipa1-NIL seeds (Figure 3C–G), although previous studies have reported that the exogenous GA application has little effect on the germination of the miR156 mutant or IPA1-OE seeds [18,22]. Altogether, these results support the hypothesis that the elevated expression of IPA1 delays seed germination and retards early seedling growth mainly through the GA pathway.

The contents of bioactive GAs were cooperatively regulated by biosynthesis and inactivation. In rice, OsGA20ox and OsGA2ox are involved in GA biosynthesis and inactive during seed germination, respectively [15,32]. To explore the mechanisms of how ipa1 downregulates the content of GAs, the expression levels of GA synthesis- and inactivation-related genes were investigated. For the GA synthesis-related genes, our results demonstrated that OsGA20ox1 was markedly downregulated in the ipa1-NIL seeds during germination (Figure 4C). Although the ChIP-qPCR and EMSA assays demonstrated that IPA1 could directly bind to the GTAC-containing regions in the promoters of the two GA synthesis-related genes OsCPS1 and OsKAO [18], no obvious difference was found in the expression of OsCPS1 and OsKAO between the NILs (Figure 4A,B). For the GA inactivation-related genes, OsGA2ox3, OsGA2ox6, OsGA2ox8, and OsGA2ox9 were generally upregulated in ipa1-NIL. Therefore, the lower expression level of the GA synthesis-related gene OsGA20ox1 and the higher level of the GA inactivation-related genes could lead to the lower contents of GAs in ipa1-NILs seeds.

The OsGAMYB gene is a GA-regulated transcription factor required for the transcriptional activation of α-amylase genes [7,33]. In the ipa1-NIL seeds, the expression level of OsGAMYB was significantly lower (Figure 3B). Meanwhile, RAmy1A and RAmy1C were significantly downregulated during the early stage of germination and RAmy3B/C, RAmy3D, and RAmy3E were also downregulated in the beginning. Interestingly, RAmy3B/C, RAmy3D, and RAmy3E, especially RAmy3D, were then upregulated quickly, which might be induced by sugar starvation as reported in the previous studies [24,25]. These observations suggested that IPA1 negatively regulates the early seedling development of rice by interfering with starch metabolism via the GA pathway.

The GA response in the aleurone cells is influenced by various factors. In recent decades, many members of the WRKY family have been reported to participate in GA-mediated seed germination. In rice, OsWRKY24 can bind to the Amy32b promoter and independently suppress GA induction of the Amy32b expression [34]. Recently, OsWRKY72 was identified as a negative regulator in rice germination to suppress GA accumulation through the “LRK1-OsKO2” pathway in the aleurone layer [35]. OsWRKY51 and OsWRKY71 function as heterologous dimers and directly interfere with GA-induced transcription factor OsGAMYB to inhibit the expression of αAmys [27,36]. Although OsWRKY51 does not bind to the Amy32b promoter in vitro, it could interact with OsWRKY71 to enhance the binding affinity of OsWRKY71 to the W-box [27]. In the present study, we found that the transcript levels of OsWRKY51 and OsWRKY71 were significantly upregulated in ipa1-NIL seeds (Figure 5A,B). As a transcription factor, IPA1 could regulate the expression of its target genes by binding to the core motif GTAC and/or TGGGCC/T in promoters [28]. Based on the results of the Y1H and transient dual-luciferase assays, our results suggested that IPA1 can directly activate the expression of OsWRKY51 and OsWRKY71 (Figure 5E,F), which further influences the binding affinity of OsGAMYB to the promoter of αAmys, thus downregulating its expression.

Recently, the expanding knowledge on IPA1 has led to the proposal of IPA1 as a pleiotropic gene to improve agronomic traits in rice [22,23]. Seed germination and early seedling development are the traits we were concerned with here. Generally, when the seeds are soaked in water, their GA level increases dramatically so as to promote seed germination [26]. In our study, the expression of IPA1 was upregulated quickly in the germinating seeds of the ipa1-NIL. Meanwhile, the GA synthesis-related gene OsGA20ox1 and the GA inactivation-related genes such as OsGA2ox3, OsGA2ox6, OsGA2ox8, and OsGA2ox9 were detected to be downregulated and upregulated, respectively. As a result, the GA level was decreased and then the expression of OsGAMYB was downregulated in ipa1-NIL. Additionally, IPA1 could promote the expression of OsWRKY51 and OsWRKY71 directly, which would influence the binding affinity of OsGAMYB to the α-amylase genes. Therefore, our results suggested that IPA1 retards seed germination and early seedling growth by interfering with starch metabolism via both the GA and WRKY pathways.

4. Materials and Methods

4.1. Plant Materials

To generate near-isogenic lines (NILs) of ipa1 and IPA1, the ipa1-containing japonica line Shaoniejing (SNJ) [19] was crossed with an indica cultivar Yuetai B (IPA1/IPA1) to develop the Yuetai B/SNJ F₁ plants. Then, the F₁ plants were backcrossed with Yuetai B to develop the BC₁F₁ plants. Subsequently, one of the BC₁F₁ plants was self-crossed for six generations to develop Yuetai B/SNJ BC₁F₇ plants. Using marker-assisted selection, a BC₁F₇ plant with the genotype IPA1/ipa1 on the IPA1 locus was obtained. In the self-crossed progeny of this BC₁F₇ plant, the plants with the genotype IPA1/IPA1 were identified as IPA1-NIL, whereas the plants with the genotype ipa1/ipa1 were identified as ipa1-NIL.

4.2. Seed Germination Analysis

Sterilized NIL seeds were incubated at 30 °C in the dark with water, 10 μM GA₃, or 30 μM GA₃. Three replicates (more than 50 seeds/replicate) were analyzed for each treatment. The seed germination rate was calculated at different time points after imbibition. A seed was considered to have germinated when the radicle or shoot length was longer than 1 mm.

4.3. Determination of α-Amylase Activity

The amylase activity was quantitatively determined by a modified version of the 3,5-dinitrosalicylic acid method, as described in previous studies [37,38]. Briefly, the seeds were incubated in the water at 28 °C. After 12 and 48 h incubation, the seeds were collected and ground in liquid nitrogen. Powder (0.5 g) was used for enzyme extraction. To determine the α-amylase activity, 1 mL crude enzyme extract was incubated in the water at 70 °C for 15 min to inhibit the activity of β-amylase. The additional 1 mL enzyme extract was not heated and used to measure the total amylase activity. Then, each enzyme extract was mixed with 1 mL of 1% (w/v) soluble starch dissolved in citric acid buffer (pH = 5.6). After heating in a water bath at 40 °C for 5 min, 2 mL 3,5-dinitrosalicylic acid reagent was added, and the mixture was boiled for 5 min. The absorbance of the mixture was measured at wavelengths of 540 nm. Three replicates were analyzed for each treatment.

4.4. Measurement of Soluble Sugar Content

The soluble sugar content was quantified by the anthrone method [39] with minor modifications. The embryos and endosperms of germinating seeds were collected from each replicate at 12, 48, and 96 h and immediately dried to a constant weight at 70 °C. Subsequently, the sample was ground, and 0.01 g powder was mixed with 800 μL of 80% (v/v) ethanol. The mixture was heated at 80 °C for 30 min, cooled, centrifuged at 3000 rpm (664× g) for 10 min, and diluted to a volume of 2 mL with 80% (v/v) ethanol. The reaction mix contained 200 μL extract and 1 mL reagent was heated at 95 °C for 15 min. The absorbance of samples was finally recorded at 620 nm. The soluble content was calculated using glucose as the standard. Three replicates were analyzed for each treatment.

4.5. Measurement of Endogenous Bioactive GA Content

The endogenous GA contents in seeds were determined as described in [40]. In brief, the dehulled seeds were ground in liquid nitrogen, and 120 mg powder was mixed with 1.2 mL 80% (v/v) methanol at 4 °C. After centrifugation at 12,000× g for 15 min at 4 °C, the supernatant was dried under a stream of N₂. Then, the residues were dissolved in 30% methanol and centrifuged. The supernatant was collected for LC-MS analysis.

4.6. RNA Extraction and qPCR

After 12, 24, 36, and 48 h incubation, total RNA from the germinating seeds was extracted with TRIzol reagent (Invitrogen, Carlsbad, CA, USA). First-strand cDNA was synthesized from 2 μg RNA in a total of 20 μL reaction system with an ABScript III RT Master Mix with gDNA Remover (ABclonal, Wuhan, China) according to the manufacturer’s instructions. Synthesized cDNAs were used for qPCR with 2× Universal SYBR Green Fast qPCR Mix (ABclonal, Wuhan, China) on a CFX384^TM real-time PCR Detection System (Bio-Rad, Hercules, CA, USA). The primers used for qPCR are listed in Table S1. PCR thermal cycling conditions were as follows: initial denaturation, 95 °C for 5 min; 40 cycles of denaturation 95 °C for 10 sec, annealing and extension at 60 °C for 30 s; followed by melting and plate reading. Three biological replicates were included for each sample. The OsActin gene expression was used as an internal control to normalize the expression of target genes.

4.7. Dual-Luciferase Assay

The dual-luciferase assays were performed according to a previously described method [29]. The promoter of OsWRKY51 and OsWRKY71 was amplified from the genomic DNA (primer pairs listed in Table S1) and cloned into the upstream of the LUC reporter gene to generate the ProOsWRKY51-LUC and ProOsWRKY71-LUC reporter construct, respectively. The luciferase gene from Renilla reniformis (Ren) under control of the CaMV 35S promoter was used as an internal control. The cDNA of IPA1 was amplified (primer pairs listed in Table S1) and inserted into the HindIII/BamHI digested pRGV vector [41] to generate the Ubi:IPA1 effector construct. The combined reporter and effector plasmids were co-transformed into rice protoplasts as described in [42]. An empty pRGV vector co-transformed with the reporter construct was used as a vector control. The LUC activity was measured with the Dual-Luciferase Assay Kit (Promega, Beijing, China) according to the manufacturer’s recommendations, and the relative LUC activity was calculated as the ratio of LUC/Ren.

4.8. Yeast One-Hybrid Assay

The coding region of IPA1-SBP was amplified by PCR and cloned into a pGADT7 vector to produce an IPA1_SBP-AD construct. Various truncated fragments of the promoter regions of OsWRKY51 and OsWRKY71 were amplified and ligated into the pABAi vector to generate the bait vectors. After linearization by the BstBI enzyme, the bait vector co-transformed with the prey vector into the yeast strain Y1HGold. The transformants were grown on SD/−Ura/−Leu plates at 30 °C for 3 days, then grown on SD/−Ura/−Leu/AbAi plates. Yeast strains containing the empty pGADT7 in combination with the bait vector were used as the negative control.