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Chromatin modification contributes to the expression divergence of three TaGS2 homoeologs in hexaploid wheat

机译:染色质修饰有助于六倍体小麦中三个TaGS2同源物的表达差异

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摘要

Plastic glutamine synthetase (GS2) is responsible for ammonium assimilation. The reason that TaGS2 homoeologs in hexaploid wheat experience different selection pressures in the breeding process remains unclear. TaGS2 were minimally expressed in roots but predominantly expressed in leaves, and TaGS2-B had higher expression than TaGS2-A and TaGS2-D. ChIP assays revealed that the activation of TaGS2-B expression in leaves was correlated with increased H3K4 trimethylation. The transcriptional silencing of TaGS2 in roots was correlated with greater cytosine methylation and less H3K4 trimethylation. Micrococcal nuclease and DNase I accessibility experiments indicated that the promoter region was more resistant to digestion in roots than leaves, which indicated that the closed nucleosome conformation of the promoter region was important to the transcription initiation for the spatial-temporal expression of TaGS2. In contrast, the transcribed regions possess different nuclease accessibilities of three TaGS2 homoeologs in the same tissue, suggesting that nucleosome conformation of the transcribed region was part of the fine adjustment of TaGS2 homoeologs. This study provides evidence that histone modification, DNA methylation and nuclease accessibility coordinated the control of the transcription of TaGS2 homoeologs. Our results provided important evidence that TaGS2-B experienced the strongest selection pressures during the breeding process.
机译:塑料谷氨酰胺合成酶(GS2)负责铵同化作用。尚不清楚六倍体小麦中TaGS2同源物在选择过程中经历不同选择压力的原因。 TaGS2在根中表达最少,但主要在叶中表达,并且TaGS2-B的表达高于TaGS2-A和TaGS2-D。 ChIP分析显示,叶片中TaGS2-B表达的激活与H3K4三甲基化增加有关。 TaGS2在根中的转录沉默与更高的胞嘧啶甲基化和更少的H3K4三甲基化相关。微球菌核酸酶和DNase I的可及性实验表明,启动子区域对根部的消化比对叶片更具抵抗力,这表明启动子区域的闭合核小体构象对于TaGS2的时空表达转录起始很重要。相反,转录的区域在同一组织中具有三个TaGS2同源物的不同核酸酶可及性,表明转录区的核小体构象是TaGS2同源物的微调的一部分。这项研究提供的证据表明,组蛋白修饰,DNA甲基化和核酸酶可及性协调了TaGS2同源物转录的控制。我们的结果提供了重要的证据,表明TaGS2-B在育种过程中经历了最强的选择压力。

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