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本文引用的文献

1
Ethylene induces combinatorial effects of histone H3 acetylation in gene expression in Arabidopsis.乙烯在拟南芥基因表达中诱导组蛋白H3乙酰化的组合效应。
BMC Genomics. 2017 Jul 17;18(1):538. doi: 10.1186/s12864-017-3929-6.
2
Phosphorylation of CBP20 Links MicroRNA to Root Growth in the Ethylene Response.CBP20的磷酸化作用将微小RNA与乙烯反应中的根系生长联系起来。
PLoS Genet. 2016 Nov 21;12(11):e1006437. doi: 10.1371/journal.pgen.1006437. eCollection 2016 Nov.
3
EIN2-dependent regulation of acetylation of histone H3K14 and non-canonical histone H3K23 in ethylene signalling.EIN2 依赖性调节乙烯信号传导中组蛋白 H3K14 和非典型组蛋白 H3K23 的乙酰化。
Nat Commun. 2016 Oct 3;7:13018. doi: 10.1038/ncomms13018.
4
Cryptochromes Interact Directly with PIFs to Control Plant Growth in Limiting Blue Light.隐花色素直接与光敏色素相互作用因子相互作用,以控制弱蓝光下的植物生长。
Cell. 2016 Jan 14;164(1-2):233-245. doi: 10.1016/j.cell.2015.12.018. Epub 2015 Dec 24.
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Histone deacetylation-mediated cellular dedifferentiation in Arabidopsis.拟南芥中组蛋白去乙酰化介导的细胞去分化
J Plant Physiol. 2016 Feb 1;191:95-100. doi: 10.1016/j.jplph.2015.12.006. Epub 2015 Dec 15.
6
Transcriptome-Wide Identification of RNA Targets of Arabidopsis SERINE/ARGININE-RICH45 Uncovers the Unexpected Roles of This RNA Binding Protein in RNA Processing.拟南芥富含丝氨酸/精氨酸蛋白45的RNA靶标的全转录组鉴定揭示了这种RNA结合蛋白在RNA加工中的意外作用。
Plant Cell. 2015 Dec;27(12):3294-308. doi: 10.1105/tpc.15.00641. Epub 2015 Nov 24.
7
Epigenetic Modifications and Plant Hormone Action.表观遗传修饰与植物激素作用
Mol Plant. 2016 Jan 4;9(1):57-70. doi: 10.1016/j.molp.2015.10.008. Epub 2015 Oct 28.
8
Gene-specific translation regulation mediated by the hormone-signaling molecule EIN2.激素信号分子 EIN2 介导的基因特异性翻译调控。
Cell. 2015 Oct 22;163(3):684-97. doi: 10.1016/j.cell.2015.09.036.
9
EIN2-directed translational regulation of ethylene signaling in Arabidopsis.EIN2 指导的拟南芥乙烯信号转导的翻译调控。
Cell. 2015 Oct 22;163(3):670-83. doi: 10.1016/j.cell.2015.09.037.
10
Auxin-regulated chromatin switch directs acquisition of flower primordium founder fate.生长素调节的染色质开关引导花原基起始细胞命运的获得。
Elife. 2015 Oct 13;4:e09269. doi: 10.7554/eLife.09269.

EIN2 介导乙烯响应中组蛋白乙酰化的直接调控。

EIN2 mediates direct regulation of histone acetylation in the ethylene response.

机构信息

Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX 78712.

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712.

出版信息

Proc Natl Acad Sci U S A. 2017 Sep 19;114(38):10274-10279. doi: 10.1073/pnas.1707937114. Epub 2017 Sep 5.

DOI:10.1073/pnas.1707937114
PMID:28874528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5617289/
Abstract

Ethylene gas is essential for developmental processes and stress responses in plants. Although the membrane-bound protein EIN2 is critical for ethylene signaling, the mechanism by which the ethylene signal is transduced remains largely unknown. Here we show the levels of H3K14Ac and H3K23Ac are correlated with the levels of EIN2 protein and demonstrate EIN2 C terminus (EIN2-C) is sufficient to rescue the levels of H3K14/23Ac of at the target loci, using CRISPR/dCas9-EIN2-C. Chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) and ChIP-reChIP-seq analyses revealed that EIN2-C associates with histone partially through an interaction with EIN2 nuclear-associated protein1 (ENAP1), which preferentially binds to the genome regions that are associated with actively expressed genes both with and without ethylene treatments. Specifically, in the presence of ethylene, ENAP1-binding regions are more accessible upon the interaction with EIN2, and more EIN3 proteins bind to the loci where ENAP1 is enriched for a quick response. Together, these results reveal EIN2-C is the key factor regulating H3K14Ac and H3K23Ac in response to ethylene and uncover a unique mechanism by which ENAP1 interacts with chromatin, potentially preserving the open chromatin regions in the absence of ethylene; in the presence of ethylene, EIN2 interacts with ENAP1, elevating the levels of H3K14Ac and H3K23Ac, promoting more EIN3 binding to the targets shared with ENAP1 and resulting in a rapid transcriptional regulation.

摘要

乙烯气体对植物的发育过程和应激反应至关重要。虽然膜结合蛋白 EIN2 对乙烯信号转导至关重要,但乙烯信号转导的机制在很大程度上仍然未知。在这里,我们展示了 H3K14Ac 和 H3K23Ac 的水平与 EIN2 蛋白的水平相关,并证明使用 CRISPR/dCas9-EIN2-C,EIN2 C 端(EIN2-C)足以挽救靶基因座上的 H3K14/23Ac 的水平。染色质免疫沉淀 followed by deep sequencing (ChIP-seq) 和 ChIP-reChIP-seq 分析表明,EIN2-C 通过与 EIN2 核相关蛋白 1 (ENAP1) 的相互作用与组蛋白部分相关,ENAP1 优先结合与有和没有乙烯处理的活跃表达基因相关的基因组区域。具体来说,在乙烯存在的情况下,ENAP1 与 EIN2 的相互作用使 ENAP1 结合区域更容易接近,并且更多的 EIN3 蛋白结合到 ENAP1 富集的位点,以快速响应。总之,这些结果揭示了 EIN2-C 是调节乙烯反应中 H3K14Ac 和 H3K23Ac 的关键因素,并揭示了 ENAP1 与染色质相互作用的独特机制,可能在没有乙烯的情况下保留开放染色质区域;在乙烯存在的情况下,EIN2 与 ENAP1 相互作用,提高 H3K14Ac 和 H3K23Ac 的水平,促进更多的 EIN3 与与 ENAP1 共享的靶标结合,并导致快速的转录调控。