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组蛋白 H1 缺失的脊椎动物细胞表现出核小体结构的改变。

Histone H1 null vertebrate cells exhibit altered nucleosome architecture.

机构信息

Experimental Research Center for Infectious Diseases, Institute for Virus Research, Kyoto University, Kyoto, Japan.

出版信息

Nucleic Acids Res. 2010 Jun;38(11):3533-45. doi: 10.1093/nar/gkq076. Epub 2010 Feb 15.

DOI:10.1093/nar/gkq076
PMID:20156997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2887950/
Abstract

In eukaryotic nuclei, DNA is wrapped around an octamer of core histones to form nucleosomes, and chromatin fibers are thought to be stabilized by linker histones of the H1 type. Higher eukaryotes express multiple variants of histone H1; chickens possess six H1 variants. Here, we generated and analyzed the phenotype of a complete deletion of histone H1 genes in chicken cells. The H1-null cells showed decreased global nucleosome spacing, expanded nuclear volumes, and increased chromosome aberration rates, although proper mitotic chromatin structure appeared to be maintained. Expression array analysis revealed that the transcription of multiple genes was affected and was mostly downregulated in histone H1-deficient cells. This report describes the first histone H1 complete knockout cells in vertebrates and suggests that linker histone H1, while not required for mitotic chromatin condensation, plays important roles in nucleosome spacing and interphase chromatin compaction and acts as a global transcription regulator.

摘要

在真核细胞核中,DNA 缠绕在核心组蛋白的八聚体周围形成核小体,染色质纤维被认为通过 H1 型连接组蛋白稳定。高等真核生物表达多种组蛋白 H1 变体;鸡拥有六种 H1 变体。在这里,我们生成并分析了鸡细胞中组蛋白 H1 基因完全缺失的表型。H1 缺失细胞表现出全局核小体间距减小、核体积增大和染色体畸变率增加,尽管有适当的有丝分裂染色质结构。表达谱分析显示,多个基因的转录受到影响,在缺乏组蛋白 H1 的细胞中大多下调。本报告描述了脊椎动物中第一个组蛋白 H1 完全敲除细胞,并表明连接组蛋白 H1 虽然不是有丝分裂染色质凝聚所必需的,但在核小体间距和有丝分裂间期染色质紧缩中发挥重要作用,并作为一个全局转录调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/8068136cc55e/gkq076f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/792a765fa8bc/gkq076f1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/630840713138/gkq076f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/66d058e8a316/gkq076f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/94fd62343913/gkq076f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/30cef5408e14/gkq076f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/8068136cc55e/gkq076f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/792a765fa8bc/gkq076f1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/630840713138/gkq076f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/66d058e8a316/gkq076f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/94fd62343913/gkq076f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/30cef5408e14/gkq076f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b1/2887950/8068136cc55e/gkq076f6.jpg

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本文引用的文献

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Genes Dev. 2009 Feb 15;23(4):452-65. doi: 10.1101/gad.1749309. Epub 2009 Feb 4.
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Depletion of human histone H1 variants uncovers specific roles in gene expression and cell growth.人类组蛋白H1变体的缺失揭示了其在基因表达和细胞生长中的特定作用。
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Histone H1 variant, H1R is involved in DNA damage response.
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Histone H1.5 binds over splice sites in chromatin and regulates alternative splicing.组蛋白 H1.5 结合在染色质的剪接位点上,并调节可变剪接。
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A nucleosome-free region locally abrogates histone H1-dependent restriction of linker DNA accessibility in chromatin.无核小体区域局部消除了组蛋白 H1 对染色质中环连 DNA 可及性的依赖限制。
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