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酵母应激反应过程中的高分辨率染色质动力学

High-resolution chromatin dynamics during a yeast stress response.

作者信息

Weiner Assaf, Hsieh Tsung-Han S, Appleboim Alon, Chen Hsiuyi V, Rahat Ayelet, Amit Ido, Rando Oliver J, Friedman Nir

机构信息

School of Computer Science and Engineering, The Hebrew University, Jerusalem 9190401, Israel; Institute of Life Sciences, The Hebrew University, Jerusalem 9190401, Israel.

Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Mol Cell. 2015 Apr 16;58(2):371-86. doi: 10.1016/j.molcel.2015.02.002. Epub 2015 Mar 19.

Abstract

Covalent histone modifications are highly conserved and play multiple roles in eukaryotic transcription regulation. Here, we mapped 26 histone modifications genome-wide in exponentially growing yeast and during a dramatic transcriptional reprogramming-the response to diamide stress. We extend prior studies showing that steady-state histone modification patterns reflect genomic processes, especially transcription, and display limited combinatorial complexity. Interestingly, during the stress response we document a modest increase in the combinatorial complexity of histone modification space, resulting from roughly 3% of all nucleosomes transiently populating rare histone modification states. Most of these rare histone states result from differences in the kinetics of histone modification that transiently uncouple highly correlated marks, with slow histone methylation changes often lagging behind the more rapid acetylation changes. Explicit analysis of modification dynamics uncovers ordered sequences of events in gene activation and repression. Together, our results provide a comprehensive view of chromatin dynamics during a massive transcriptional upheaval.

摘要

共价组蛋白修饰高度保守,在真核生物转录调控中发挥多种作用。在此,我们在指数生长的酵母中以及在剧烈的转录重编程过程中——对二酰胺应激的反应——全基因组绘制了26种组蛋白修饰。我们扩展了先前的研究,这些研究表明稳态组蛋白修饰模式反映基因组过程,尤其是转录,并显示出有限的组合复杂性。有趣的是,在应激反应过程中,我们记录到组蛋白修饰空间的组合复杂性适度增加,这是由于所有核小体中约3%的核小体瞬时占据罕见的组蛋白修饰状态所致。这些罕见的组蛋白状态大多源于组蛋白修饰动力学的差异,这些差异使高度相关的标记瞬时解偶联,组蛋白甲基化变化缓慢,往往滞后于更快的乙酰化变化。对修饰动力学的明确分析揭示了基因激活和抑制过程中有序的事件序列。总之,我们的结果提供了大规模转录剧变过程中染色质动力学的全面视图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0139/4405355/eca2d935f57f/fx1.jpg

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