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启动子相关的组蛋白乙酰化参与了渗透胁迫诱导的玉米ZmDREB2A基因的转录调控。

Promoter-associated histone acetylation is involved in the osmotic stress-induced transcriptional regulation of the maize ZmDREB2A gene.

作者信息

Zhao Lin, Wang Pu, Yan Shihan, Gao Fei, Li Hui, Hou Haoli, Zhang Qi, Tan Junjun, Li Lijia

机构信息

State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan, 430072, China.

出版信息

Physiol Plant. 2014 Aug;151(4):459-67. doi: 10.1111/ppl.12136. Epub 2013 Dec 27.

DOI:10.1111/ppl.12136
PMID:24299295
Abstract

Epigenetic modifications play a key role in the transcriptional regulation of stress-induced gene expression in plants. In this study, we showed that the overall acetylation levels of histone H3 lysine 9 (H3K9) and H4 lysine 5 (H4K5) in the genome were increased in maize seedlings after mannitol treatment (to mimic osmotic stress). Mannitol treatment significantly induced the upregulation of the maize osmotic stress responsive gene Zea mays dehydration-responsive element binding protein 2A (ZmDREB2A), whereas abscisic acid (ABA) did not result in the induction of this gene. The application of exogenous ABA under osmotic stress conditions strongly repressed the induction of the ZmDREB2A gene. Chromatin immunoprecipitation and chromatin accessibility by real-time PCR experiments revealed that the promoter region of the ZmDREB2A gene was quickly hyperacetylated and decondensed after the mannitol treatment, suggesting that the promoter region is poised for histone acetylation to allow for fast induction of the ZmDREB2A gene. However, under osmotic stress conditions, the ABA treatment decreased the acetylation status and chromatin accessibility to micrococcal nuclease. These results suggest that osmotic stress activates the transcription of the ZmDREB2A gene by increasing the levels of acetylated histones H3K9 and H4K5 associated with the ZmDREB2A promoter region.

摘要

表观遗传修饰在植物应激诱导基因表达的转录调控中起关键作用。在本研究中,我们发现甘露醇处理(模拟渗透胁迫)后,玉米幼苗基因组中组蛋白H3赖氨酸9(H3K9)和H4赖氨酸5(H4K5)的整体乙酰化水平升高。甘露醇处理显著诱导了玉米渗透胁迫响应基因玉米脱水响应元件结合蛋白2A(ZmDREB2A)的上调,而脱落酸(ABA)并未诱导该基因。在渗透胁迫条件下施加外源ABA强烈抑制了ZmDREB2A基因的诱导。染色质免疫沉淀和实时PCR实验检测的染色质可及性表明,甘露醇处理后ZmDREB2A基因的启动子区域迅速发生超乙酰化并解聚,这表明该启动子区域处于组蛋白乙酰化状态以便快速诱导ZmDREB2A基因。然而,在渗透胁迫条件下,ABA处理降低了乙酰化状态以及微球菌核酸酶对染色质的可及性。这些结果表明,渗透胁迫通过增加与ZmDREB2A启动子区域相关的组蛋白H3K9和H4K5的乙酰化水平来激活ZmDREB2A基因的转录。

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