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组蛋白密码与高阶染色质折叠:一种假说。

Histone Code and Higher-Order Chromatin Folding: A Hypothesis.

作者信息

Prakash Kirti, Fournier David

机构信息

Department of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA.

Faculty of Biology and Center for Computational Sciences, Johannes Gutenberg University Mainz, 55128 Mainz, Germany.

出版信息

Genom Comput Biol. 2017;3(2). doi: 10.18547/gcb.2017.vol3.iss2.e41. Epub 2017 Jan 30.

Abstract

Histone modifications alone or in combination are thought to modulate chromatin structure and function; a concept termed histone code. By combining evidence from several studies, we investigated if the histone code can play a role in higher-order folding of chromatin. Firstly using genomic data, we analyzed associations between histone modifications at the nucleosome level. We could dissect the composition of individual nucleosomes into five predicted clusters of histone modifications. Secondly, by assembling the raw reads of histone modifications at various length scales, we noticed that the histone mark relationships that exist at nucleosome level tend to be maintained at the higher orders of chromatin folding. Recently, a high-resolution imaging study showed that histone marks belonging to three of the five predicted clusters show structurally distinct and anti-correlated chromatin domains at the level of chromosomes. This made us think that the histone code can have a significant impact in the overall compaction of DNA: at the level of nucleosomes, at the level of genes, and finally at the level of chromosomes. As a result, in this article, we put forward a theory where the histone code drives not only the functionality but also the higher-order folding and compaction of chromatin.

摘要

单独或组合的组蛋白修饰被认为可调节染色质结构和功能;这一概念被称为组蛋白密码。通过整合多项研究的证据,我们研究了组蛋白密码是否能在染色质的高级折叠中发挥作用。首先,利用基因组数据,我们分析了核小体水平上组蛋白修饰之间的关联。我们可以将单个核小体的组成解析为五个预测的组蛋白修饰簇。其次,通过在各种长度尺度上组装组蛋白修饰的原始读数,我们注意到在核小体水平上存在的组蛋白标记关系在染色质折叠的更高层次上往往得以维持。最近,一项高分辨率成像研究表明,属于五个预测簇中三个簇的组蛋白标记在染色体水平上显示出结构上不同且反相关的染色质结构域。这使我们认为组蛋白密码可能对DNA的整体压缩有重大影响:在核小体水平、基因水平,最终在染色体水平。因此,在本文中,我们提出了一种理论,即组蛋白密码不仅驱动染色质的功能,还驱动染色质的高级折叠和压缩。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c830/6594697/1870c25697ff/nihms-1036474-f0001.jpg

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