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

机译:染色质改性有助于三个标签2在六倍体小麦中的三个标签2同源物的发散

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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。标签2在六倍体小麦中的同源素在繁殖过程中经历不同的选择压力的原因尚不清楚。标签2在根中以根本表示,但主要在叶子中表达,而TAGS2-B的表达比TAGS2-A和TAGS2-D更高。芯片测定显示,叶片中的标签2-B表达的活化与H3K4三甲基化增加相关。标签2在根中的转录沉默与更大的胞嘧啶甲基化和更少的H3K4三甲基化相关。微息肉核酸酶和DNase I可访问性实验表明,启动子区域比叶片在根中的消化更耐消化,这表明启动子区域的闭合核体构象对TABS2的空间表达的转录起始至关重要。相反,转录区域在同一组织中具有三个标签2同源物质的不同核酸酶可见度,表明转录区域的核心符合是标签2同源物质的微调的一部分。本研究规定了组蛋白改性,DNA甲基化和核酸酶可达性协调标签2同源物的转录的控制。我们的结果提供了重要的证据,即Tags2-B在繁殖过程中经历了最强的选择压力。

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