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核小体滑动在蛋白质靶标搜索被覆盖 DNA 位点中的作用。

Role of Nucleosome Sliding in the Protein Target Search for Covered DNA Sites.

机构信息

Center for Theoretical Biological Physics, Rice University, Houston, Texas 77005, United States.

Department of Chemistry, Rice University, Houston, Texas 77005, United States.

出版信息

J Phys Chem Lett. 2023 Aug 10;14(31):7073-7082. doi: 10.1021/acs.jpclett.3c01704. Epub 2023 Aug 1.

Abstract

Associations of transcription factors (TFs) with specific sites on DNA initiate major cellular processes. But DNA in eukaryotic cells is covered by nucleosomes which prevent TFs from binding. However, nucleosome structures on DNA are not static and exhibit breathing and sliding. We develop a theoretical framework to investigate the effect of nucleosome sliding on a protein target search. By analysis of a discrete-state stochastic model of nucleosome sliding, search dynamics are explicitly evaluated. It is found that for long sliding lengths the target search dynamics are faster for normal TFs that cannot enter the nucleosomal DNA. But for more realistic short sliding lengths, the so-called pioneer TFs, which can invade nucleosomal DNA, locate specific sites faster. It is also suggested that nucleosome breathing, which is a faster process, has a stronger effect on protein search dynamics than that of nucleosome sliding. Theoretical arguments to explain these observations are presented.

摘要

转录因子 (TFs) 与 DNA 上特定位置的结合启动了主要的细胞过程。但是真核细胞中的 DNA 被核小体覆盖,核小体阻止 TFs 结合。然而,DNA 上的核小体结构并不是静态的,它们会发生呼吸和滑动。我们开发了一个理论框架来研究核小体滑动对蛋白质靶标搜索的影响。通过对核小体滑动的离散状态随机模型的分析,明确评估了搜索动力学。结果发现,对于较长的滑动长度,无法进入核小体 DNA 的正常 TF 的搜索动力学更快。但是对于更现实的较短滑动长度,即所谓的可以侵入核小体 DNA 的先驱 TF,它们可以更快地定位特定的位点。此外,研究还表明,呼吸作用是一个更快的过程,它对蛋白质搜索动力学的影响比核小体滑动更大。提出了一些理论观点来解释这些观察结果。

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