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组蛋白H2A泛素化并不排除组蛋白H1的结合,但它促进了组蛋白H1与核小体的结合。

Histone H2A ubiquitination does not preclude histone H1 binding, but it facilitates its association with the nucleosome.

作者信息

Jason Laure J M, Finn Ron M, Lindsey George, Ausió Juan

机构信息

Biacore Incorporated, Piscataway, New Jersey 08854, USA.

出版信息

J Biol Chem. 2005 Feb 11;280(6):4975-82. doi: 10.1074/jbc.M410203200. Epub 2004 Nov 16.

Abstract

Histone H2A ubiquitination is a bulky posttranslational modification that occurs at the vicinity of the binding site for linker histones in the nucleosome. Therefore, we took several experimental approaches to investigate the role of ubiquitinated H2A (uH2A) in the binding of linker histones. Our results showed that uH2A was present in situ in histone H1-containing nucleosomes. Notably in vitro experiments using nucleosomes reconstituted onto 167-bp random sequence and 208-bp (5 S rRNA gene) DNA fragments showed that ubiquitination of H2A did not prevent binding of histone H1 but it rather enhanced the binding of this histone to the nucleosome. We also showed that ubiquitination of H2A did not affect the positioning of the histone octamer in the nucleosome in either the absence or the presence of linker histones.

摘要

组蛋白H2A泛素化是一种发生在核小体中连接组蛋白结合位点附近的大规模翻译后修饰。因此,我们采用了多种实验方法来研究泛素化H2A(uH2A)在连接组蛋白结合中的作用。我们的结果表明,uH2A原位存在于含组蛋白H1的核小体中。值得注意的是,使用重组到167bp随机序列和208bp(5S rRNA基因)DNA片段上的核小体进行的体外实验表明,H2A的泛素化并不阻止组蛋白H1的结合,反而增强了该组蛋白与核小体的结合。我们还表明,无论是否存在连接组蛋白,H2A的泛素化都不会影响组蛋白八聚体在核小体中的定位。

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