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