LpSAPK9 phosphorylates and activates LpABF2/LpABF3 to transactivate expression of chlorophyll catabolic genes and promote leaf senescence in perennial ryegrass

IF 5.7 1区 生物学 Q1 PLANT SCIENCES
Yuwei Yang, Jing Xing, Huanhuan Hao, Hao Guan, Huadong Yang, Tingchao Yin, Yingjun Chi, Bin Xu, Jing Zhang
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引用次数: 0

Abstract

Leaf senescence is an active and tightly controlled process that is particularly important for perennial plants to survive over hostile environmental conditions. The phytohormone ABA plays a vital regulatory role in leaf senescence, and the subclass III SnRK2 family genes, such as SnRK2.2/2.3/2.6, are known as key components in ABA signaling. Yet, the functional roles and molecular mechanisms of subclass I SnRK2s in ABA-mediated leaf senescence remain less well understood. In this study, we characterized one subclass I SnRK2 kinase, LpSAPK9, in perennial ryegrass (Lolium perenne). LpSAPK9 was localized in both the chloroplast and the nucleus, and its gene expression was positively correlated with the process of leaf senescence. Overexpressing LpSAPK9 accelerated developmental and drought/osmotic-induced leaf senescence. The interactive proteins of LpSAPK9, including LpABF2 and LpABF3, were identified using yeast two-hybrid (Y2H) library screening and confirmed by firefly luciferase complementation assay (LCA), bimolecular fluorescence complementation (BiFC), and co-immunoprecipitation (Co-IP) assays. Combining Y1H, in planta transactivation assay, and CUT&Tag-qPCR, we identified that LpABF2 and LpABF3 directly bound promoters of four chlorophyll catabolic genes (LpSGR, LpNYC1, LpNOL, and LpPPH) to activate their transcription. By phosphorylating the S89 and T130 amino acid residues in LpABF2 and the S122 in LpABF3, LpSAPK9 enhances the transcription activities of LpABF2/3 to promote chlorophyll degradation and leaf senescence. Interestingly, LpSAPK9 overexpression not only accelerated these senescence processes but also reduced leaf ABA content and down-regulated ABA biosynthetic genes. Collectively, our results reveal that the LpSAPK9-LpABF2/LpABF3 module coordinately regulates the expression of chlorophyll catabolic genes to control leaf senescence in perennial ryegrass.

LpSAPK9磷酸化并激活LpABF2/LpABF3,反激活叶绿素分解代谢基因的表达,促进多年生黑麦草叶片衰老。
叶片衰老是一个主动和严格控制的过程,对多年生植物在恶劣的环境条件下生存尤为重要。植物激素ABA在叶片衰老过程中起着重要的调控作用,而SnRK2家族III亚类基因SnRK2.2/2.3/2.6是ABA信号传导的关键成分。然而,SnRK2s亚类在aba介导的叶片衰老中的功能作用和分子机制尚不清楚。在本研究中,我们鉴定了多年生黑麦草(Lolium perenne)中SnRK2激酶的一个亚类LpSAPK9。LpSAPK9定位于叶绿体和细胞核,其基因表达与叶片衰老过程呈正相关。过表达LpSAPK9加速了发育和干旱/渗透诱导的叶片衰老。通过酵母双杂交(Y2H)文库筛选鉴定LpSAPK9的互作蛋白LpABF2和LpABF3,并通过萤火虫荧光素酶互补实验(LCA)、双分子荧光互补实验(BiFC)和共免疫沉淀实验(Co-IP)进行鉴定。结合Y1H、in plant transactivation assay和CUT&Tag-qPCR,我们发现LpABF2和LpABF3直接结合4个叶绿素分解代谢基因(LpSGR、LpNYC1、LpNOL和LpPPH)的启动子来激活它们的转录。LpSAPK9通过磷酸化LpABF2中的S89和T130氨基酸残基以及LpABF3中的S122氨基酸残基,增强LpABF2/3的转录活性,促进叶绿素降解和叶片衰老。有趣的是,LpSAPK9过表达不仅加速了这些衰老过程,而且降低了叶片ABA含量,下调了ABA生物合成基因。综上所述,LpSAPK9-LpABF2/LpABF3模块协同调节叶绿素分解代谢基因的表达,控制多年生黑麦草叶片衰老。
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来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
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