National Agri-Food Biotechnology Institute, Knowledge City Sector-81, Mohali, Punjab, 140306, India.
Department of Biotechnology, Panjab University, Chandigarh, 160014, India.
Mol Biol Rep. 2021 Mar;48(3):2473-2483. doi: 10.1007/s11033-021-06282-4. Epub 2021 Apr 8.
Starch is biosynthesized during seed development and this process is regulated by many bZIP proteins in bread wheat. Abscisic acid (ABA), an important phyto-hormone involved in various physiological processes mediated by bZIPs in plants including seed development. The 'Group A' TabZIP transcription factors play important roles in the ABA signaling pathway in Arabidopsis, rice and other cereal crops but their role in regulation of amylose biosynthesis in wheat is limited. In this study 83 'Group A' TabZIPs were characterized by gene expression analysis in wheat amylose mutants. A set of 17 TabZIPs was selected on the basis of differential expression (> 2 fold) in low and high amylose mutants from RNA-seq data and validated by qRT PCR. Based on qRT PCR and correlation analysis out of the 17 TabZIPs six differentially expressed candidate TabZIPs were identified, involving in high amylose biosynthesis. The TabZIP175.2, identified as upregulated in all high amylose lines and TabZIP90.2, TabZIP129.1, TabZIP132.2, TabZIP143 and TabZIP159.2 were found downregulated in all low amylose lines, after exogenous supply of ABA. Proximal promoter analysis of starch pathway genes revealed the presence of ABA-responsive elements (ABREs) that are putative binding sites for bZIPs. Collectively, these findings indicated the involvement of putative six candidate TabZIPs as transcriptional regulators of amylose related genes via an ABA-dependent pathway in wheat. This study could help the investigators to make an informed decision to edit wheat genome for high/low amylose content using gene-editing technologies.
淀粉在种子发育过程中生物合成,这一过程受到许多面包小麦 bZIP 蛋白的调节。脱落酸(ABA)是一种重要的植物激素,参与植物中 bZIP 介导的各种生理过程,包括种子发育。“A 组”TabZIP 转录因子在拟南芥、水稻和其他谷类作物的 ABA 信号通路中发挥重要作用,但它们在调节小麦直链淀粉生物合成中的作用有限。本研究通过对小麦直链淀粉突变体的基因表达分析,对 83 个“A 组”TabZIP 进行了特征描述。根据 RNA-seq 数据中低直链淀粉和高直链淀粉突变体之间差异表达(>2 倍),选择了一组 17 个 TabZIP,并通过 qRT-PCR 进行了验证。基于 qRT-PCR 和相关性分析,从 17 个 TabZIP 中鉴定出 6 个差异表达的候选 TabZIP,涉及高直链淀粉生物合成。TabZIP175.2 在所有高直链淀粉系中均上调表达,TabZIP90.2、TabZIP129.1、TabZIP132.2、TabZIP143 和 TabZIP159.2 在所有低直链淀粉系中均下调表达,这是在外源 ABA 供应后的结果。淀粉途径基因的近端启动子分析表明存在 ABA 反应元件(ABREs),这些元件是 bZIP 的假定结合位点。综上所述,这些发现表明,在小麦中,六个假定的候选 TabZIP 作为直链淀粉相关基因的转录调节剂,通过 ABA 依赖途径参与直链淀粉的生物合成。本研究可以帮助研究人员在使用基因编辑技术编辑小麦基因组以获得高/低直链淀粉含量时做出明智的决策。