拟南芥热胁迫期间蛋白质 SUMOylation 在 miRNA 转录调控中的功能表征

Simin Xia, Yue Chen, Jianbin Lai, Zhonghui Zhang, Chengwei Yang, Danlu Han
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引用次数: 0

摘要

微RNA(miRNA)作为非编码RNA类型的表观遗传调节因子,在植物应对高温胁迫的过程中发挥着重要作用。在 SUMO(小泛素相关修饰因子)胁迫响应(SSR)中,miRNAs 对全局转录调控起着至关重要的作用。然而,其下游调控的分子机制仍不清楚。在本研究中,SUMO 特异性染色质免疫沉淀测序分析检测到了高温胁迫下 miRNA 启动子区域的特异性结合。这种结合与 miRNA 图谱之间的相关性分析表明,SUMO 在染色体上的位置与 miRNA 的表达模式相关,尤其是 miR398a 和 miR824a。相比之下,拟南芥中依赖 SSR 的 SUMO E3 连接酶 SAP AND MIZ 1 的基因敲除突变体与野生型相比,在 SUMO 相关 miRNA 的靶基因表达方面表现出相反的趋势。多组学相关分析发现了 34 个可能参与调控 miRNA 对高温胁迫响应的 SUMO 候选蛋白。因此,我们提出了一个潜在的模型,即高温暴露诱导 SUMO 分子进入细胞核,从而修饰与 miRNA 基因启动子结合的特定转录因子,并可能调控 miRNA 的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional characterization of protein SUMOylation in the miRNA transcription regulation during heat stress in Arabidopsis
MicroRNAs (miRNAs) play an essential role as non‐coding‐RNA‐type epigenetic regulators in response to high‐temperature stress in plants. There are crucial roles for global transcriptional regulation under SUMO (small ubiquitin‐related MOdifier) stress response (SSR). However, the molecular mechanisms underlying its downstream regulation remain unclear. In this study, SUMO‐specific chromatin immunoprecipitation sequencing analysis detected specific binding in the promoter region of miRNAs under high‐temperature stress. A correlation analysis between this binding and miRNA profiling revealed that the location of SUMO on the chromosome was correlated with the expression pattern of miRNAs, particularly miR398a and miR824a. In contrast, knockout mutants of the SSR‐dependent SUMO E3 ligase SAP AND MIZ 1 in Arabidopsis exhibited opposing trends in target gene expression for the SUMO‐related miRNAs compared to the wild type. Multi‐omics correlation analyses identified 34 SUMO‐candidate proteins that might be involved in the regulation of miRNA response to high‐temperature stress. Therefore, we propose a potential model whereby high‐temperature exposure induces nuclear entry of SUMO molecules, modifying specific transcription factors that bind to miRNA gene promoters and potentially regulate miRNA expression.
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