FORKHEAD BOX1通过组蛋白乙酰转移酶HAC1和转录因子TGA7、ABF2/3促进叶片衰老

Yaning Zhao, Hairong Liu, Jie Cao, Shuya Tan, Dawei Cheng, Shichun Li, Murao Zhang, Ruxue Zhang, Zhonghai Li
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引用次数: 0

摘要

叶片衰老是一个受复杂遗传和表观遗传网络影响的严格调控的发育过程。在这里,我们发现了AtFOX1,一个以前未被表征的叉头盒蛋白,在拟南芥(Arabidopsis thaliana)中,作为叶片衰老的积极调节因子。功能缺失的AtFOX1突变体表现为延缓衰老,而过表达的AtFOX1则加速了这一过程。机制上,AtFOX1结合TGACG序列特异性结合蛋白7 (TGA7)启动子中的GTAAAA基序,募集拟南芥CBP家族1组蛋白乙酰转移酶(HAC1),增强组蛋白H3赖氨酸9 (H3K9)乙酰化,促进TGA7转录。遗传分析表明,atfox1介导的衰老需要HAC1的功能,而TGA7作用于HAC1的下游。此外,TGA7直接激活ABA-RESPONSIVE ELEMENT BINDING FACTOR 2 (ABF2)和ABF3,这是aba诱导的叶片衰老的关键调节因子。ABF2/3/4功能的破坏减轻了TGA7或AtFOX1过表达引起的过早衰老表型。总之,我们的研究结果揭示了以atfox1为中心的调控模块控制拟南芥叶片衰老。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FORKHEAD BOX1 promotes leaf senescence via the histone acetyltransferase HAC1 and the transcription factors TGA7 and ABF2/3
Leaf senescence is a tightly regulated developmental process influenced by complex genetic and epigenetic networks. Here, we identified AtFOX1, a previously uncharacterized forkhead box (FOX) protein in Arabidopsis (Arabidopsis thaliana), as a positive regulator of leaf senescence. Loss-of-function AtFOX1 mutants exhibit delayed senescence, whereas AtFOX1 overexpression accelerated this process. Mechanistically, AtFOX1 binds to the GTAAAA motif in the TGACG SEQUENCE-SPECIFIC BINDING PROTEIN 7 (TGA7) promoter, recruiting ARABIDOPSIS HISTONE ACETYLTRANSFERASE OF THE CBP FAMILY 1 (HAC1) to enhance histone H3 lysine 9 (H3K9) acetylation and promote TGA7 transcription. Genetic analyses demonstrated that AtFOX1-mediated senescence requires HAC1 function, while TGA7 acts downstream of HAC1. Furthermore, TGA7 directly activates ABA-RESPONSIVE ELEMENT BINDING FACTOR 2 (ABF2) and ABF3, key regulators of age- and ABA-induced leaf senescence. Disruption of ABF2/3/4 function mitigated the premature senescence phenotype resulting from TGA7 or AtFOX1 overexpression. Collectively, our findings reveal a AtFOX1-centered regulatory module controlling leaf senescence in Arabidopsis.
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