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首页> 外文期刊>Plant physiology >The single-stranded DNA-binding protein WHIRLY1 represses WRKY53 expression and delays leaf senescence in a developmental stage-dependent manner in arabidopsis
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The single-stranded DNA-binding protein WHIRLY1 represses WRKY53 expression and delays leaf senescence in a developmental stage-dependent manner in arabidopsis

机译:单链DNA结合蛋白WHIRLY1抑制拟南芥中WRKY53的表达并以发育阶段依赖性的方式延迟叶片衰老。

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Leaf senescence in plants involves both positive and negative transcriptional regulation. In this work, we show evidence for the single-stranded DNA-binding protein WHIRLY1 (WHY1) that functions as an upstream suppressor of WRKY53 in a developmental stage-dependent manner during leaf senescence in Arabidopsis (Arabidopsis thaliana). The why1 mutant displayed an early-senescence phenotype. In this background, the expression levels of both WRKY53 and the senescenceassociated protease gene SAG12 increased. WHY1 bound to the sequence region that contains an elicitor response element motif-like sequence, GNNNAAATT, plus an AT-rich telomeric repeat-like sequence in the WRKY53 promoter in in vivo and in vitro mutagenesis assays as well as in a chromatin immunoprecipitation assay. This binding to the promoter of WRKY53 was regulated in a developmental stage-dependent manner, as verified by chromatin immunoprecipitation-polymerase chain reaction assay. This direct interaction was further determined by a transient expression assay in which WHY1 repressed β-GLUCURONIDASE gene expression driven by the WRKY53 promoter. Genetic analysis of double mutant transgenic plants revealed that WHY1 overexpression in the wrky53 mutant (oeWHY1wrky53) had no effect on the stay-green phenotype of the wrky53 mutant, while a WHY1 knockout mutant in the wrky53 mutant background (why1wrky53) generated subtle change in the leaf yellow/green phenotype. These results suggest that WHY1 was an upstream regulator of WRKY53 during leaf senescence.
机译:植物叶片的衰老涉及正向和负向的转录调控。在这项工作中,我们显示了单链DNA结合蛋白WHIRLY1(WHY1)的证据,该蛋白在拟南芥(Arabidopsis thaliana)叶片衰老过程中以发育阶段依赖的方式充当WRKY53的上游抑制剂。 why1突变体表现出早期衰老的表型。在这种背景下,WRKY53和衰老相关的蛋白酶基因SAG12的表达水平都增加了。 WHY1结合到在体内和体外诱变测定以及染色质免疫沉淀测定中包含在WRKY53启动子中的激发子响应元件基序样序列GNNNAAATT,以及富含AT的端粒重复序列的序列区域。如通过染色质免疫沉淀-聚合酶链反应分析所证实的,与WRKY53的启动子的这种结合以发育阶段依赖性的方式被调节。通过瞬态表达测定法进一步确定这种直接相互作用,其中WHY1抑制了由WRKY53启动子驱动的β-GLUCURONIDASE基因表达。对双突变体转基因植物的遗传分析表明,在wrky53突变体(oeWHY1wrky53)中WHY1过表达对wrky53突变体的保持绿色表型没有影响,而在wrky53突变体背景(why1wrky53)中WHY1敲除突变体在Wyy53突变体中产生了细微变化。叶黄/绿表型。这些结果表明,WHY1是叶片衰老过程中WRKY53的上游调节因子。

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