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TEM1 组合结合到并招募一个 Polycomb 因子来抑制的花发育转变。

TEM1 combinatorially binds to and recruits a Polycomb factor to repress the floral transition in .

机构信息

National Key Laboratory of Plant Molecular Genetics and Shanghai Center for Plant Stress Biology, Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 201602, China.

Key Laboratory of Molecular Design for Plant Cell Factory of Guangdong Higher Education Institutes, Institute of Plant and Food Science, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.

出版信息

Proc Natl Acad Sci U S A. 2021 Aug 31;118(35). doi: 10.1073/pnas.2103895118.

Abstract

TEMPRANILLO 1 (TEM1) is a transcriptional repressor that participates in multiple flowering pathways and negatively regulates the juvenile-to-adult transition and the flowering transition. To understand the molecular basis for the site-specific regulation of () by TEM1, we determined the structures of the two plant-specific DNA-binding domains in TEM1, AP2 and B3, in complex with their target DNA sequences from the gene 5'-untranslated region (5'-UTR), revealing the molecular basis for TEM1 specificity for its DNA targets. In vitro binding assays revealed that the combination of the AP2 and B3 binding sites greatly enhanced the overall binding of TEM1 to the 5'-UTR, indicating TEM1 combinatorically recognizes the gene 5'-UTR. We further showed that TEM1 recruits the Polycomb repressive complex 2 (PRC2) to the 5'-UTR. The simultaneous binding of the TEM1 AP2 and B3 domains to is necessary for deposition of H3K27me3 at the 5'-UTR and for the flowering repressor function of TEM1. Overall, our data suggest that the combinatorial recognition of 5'-UTR by TEM1 ensures H3K27me3 deposition to precisely regulate the floral transition.

摘要

紫鹃 1(TEM1)是一种转录抑制剂,参与多种开花途径,并负调控幼年期到成年期的过渡和开花过渡。为了了解 TEM1 对 ()的特异性调控的分子基础,我们确定了 TEM1 中两个植物特异性 DNA 结合域 AP2 和 B3 与它们的靶 DNA 序列的结构,该靶 DNA 序列来自基因 5'-非翻译区(5'-UTR),揭示了 TEM1 对其 DNA 靶标特异性的分子基础。体外结合实验表明,AP2 和 B3 结合位点的组合大大增强了 TEM1 对 5'-UTR 的整体结合,表明 TEM1 组合识别基因 5'-UTR。我们进一步表明,TEM1 将多梳抑制复合物 2(PRC2)募集到 5'-UTR。TEM1 的 AP2 和 B3 结构域同时结合到 是在 5'-UTR 处沉积 H3K27me3 和 TEM1 的开花抑制功能所必需的。总的来说,我们的数据表明,TEM1 对 5'-UTR 的组合识别确保了 H3K27me3 的沉积,从而精确地调控了花的过渡。

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