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首页> 外文期刊>Journal of Molecular Biology >Human Histone Interaction Networks: An Old Concept, New Trends
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Human Histone Interaction Networks: An Old Concept, New Trends

机译:人类组成互动网络:旧概念,新趋势

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To elucidate the properties of human histone interactions on the large scale, we perform a comprehensive mapping of human histone interaction networks by using data from structural, chemical cross-linking and various high-throughput studies. Histone interactomes derived from dierent data sources show limited overlap and complement each other. It inspires us to integrate these data into the combined histone global interaction network which includes 5308 proteins and 10,330 interactions. The analysis of topological properties of the human histone interactome reveals its scale free behavior and high modularity. Our study of histone binding interfaces uncovers a remarkably high number of residues involved in interactions between histones and non-histone proteins, 80-90% of residues in histones H3 and H4 have at least one binding partner. Two types of histone binding modes are detected: interfaces conserved in most histone variants and variant specific interfaces. Finally, dierent types of chromatin factors recognize histones in nucleosomes via distinct binding modes, and many of these interfaces utilize acidic patches among other sites. Interaction networks are available at https://github.com/Panchenko-Lab/Human-histone-interactome. (C) 2020 The Author(s). Published by Elsevier Ltd.
机译:为了在大范围内阐明人类组蛋白相互作用的性质,我们利用结构、化学交联和各种高通量研究的数据,对人类组蛋白相互作用网络进行了全面的映射。来自不同数据源的组蛋白相互作用组显示出有限的重叠和互补。它启发我们将这些数据整合到组合的组蛋白全球相互作用网络中,该网络包括5308种蛋白质和10330种相互作用。对人类组蛋白相互作用组拓扑性质的分析揭示了其无标度行为和高模块性。我们对组蛋白结合界面的研究发现,组蛋白和非组蛋白之间的相互作用涉及大量的残基,组蛋白H3和H4中80-90%的残基至少有一个结合伙伴。检测到两种组蛋白结合模式:在大多数组蛋白变体中保守的界面和变体特异性界面。最后,不同类型的染色质因子通过不同的结合模式识别核小体中的组蛋白,其中许多界面利用酸性斑块和其他位点。互动网络可在https://github.com/Panchenko-Lab/Human-histone-interactome.(C)提交人。爱思唯尔有限公司出版。

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