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亚分子细节水平的异染色质形成模拟模型。

A simulation model of heterochromatin formation at submolecular detail.

作者信息

Williams Michael R, Xiaokang Yan, Hathaway Nathaniel A, Kireev Dmitri

机构信息

Center for Integrative Chemical Biology and Drug Discovery, University of North Carolina, Chapel Hill, NC 27513, USA.

Division of Chemical Biology and Medicinal Chemistry, UNC Eshelman School of Pharmacy, Chapel Hill, NC 27599, USA.

出版信息

iScience. 2022 Jun 14;25(7):104590. doi: 10.1016/j.isci.2022.104590. eCollection 2022 Jul 15.

Abstract

Heterochromatin is a physical state of the chromatin fiber that maintains gene repression during cell development. Although evidence exists on molecular mechanisms involved in heterochromatin formation, a detailed structural mechanism of heterochromatin formation needs a better understanding. We made use of a simple Monte Carlo simulation model with explicit representation of key molecular events to observe molecular self-organization leading to heterochromatin formation. Our simulations provide a structural interpretation of several important traits of the heterochromatinization process. In particular, this study provides a depiction of how small amounts of HP1 are able to induce a highly condensed chromatin state through HP1 dimerization and bridging of sequence-remote nucleosomes. It also elucidates structural roots of a yet poorly understood phenomenon of a nondeterministic nature of heterochromatin formation and subsequent gene repression. Experimental chromatin assay provides an unbiased estimate of time scale of repressive response to a heterochromatin-triggering event.

摘要

异染色质是染色质纤维的一种物理状态,在细胞发育过程中维持基因抑制。尽管存在关于异染色质形成所涉及分子机制的证据,但异染色质形成的详细结构机制仍需更深入了解。我们利用一个简单的蒙特卡罗模拟模型,明确表示关键分子事件,以观察导致异染色质形成的分子自组织过程。我们的模拟为异染色质化过程的几个重要特征提供了结构解释。特别是,本研究描述了少量的异染色质蛋白1(HP1)如何通过HP1二聚化和连接序列遥远的核小体诱导高度浓缩的染色质状态。它还阐明了异染色质形成和随后基因抑制的非确定性这一尚未得到充分理解的现象的结构根源。实验性染色质分析为对异染色质触发事件的抑制反应的时间尺度提供了无偏差估计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42cb/9254115/4b202b8f6638/fx1.jpg

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