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本文引用的文献

1
SWI/SNF has intrinsic nucleosome disassembly activity that is dependent on adjacent nucleosomes.SWI/SNF 具有内在的核小体解组装活性,该活性依赖于相邻的核小体。
Mol Cell. 2010 May 28;38(4):590-602. doi: 10.1016/j.molcel.2010.02.040.
2
The chromatin remodeller ACF acts as a dimeric motor to space nucleosomes.染色质重塑因子 ACF 作为二聚体马达将核小体隔开。
Nature. 2009 Dec 24;462(7276):1016-21. doi: 10.1038/nature08621.
3
Differential cofactor requirements for histone eviction from two nucleosomes at the yeast PHO84 promoter are determined by intrinsic nucleosome stability.酵母PHO84启动子处两个核小体上组蛋白去除的差异辅因子需求由内在核小体稳定性决定。
Mol Cell Biol. 2009 Jun;29(11):2960-81. doi: 10.1128/MCB.01054-08. Epub 2009 Mar 23.
4
Activator-dependent recruitment of SWI/SNF and INO80 during INO1 activation.INO1激活过程中依赖激活因子的SWI/SNF和INO80募集
Biochem Biophys Res Commun. 2008 Sep 5;373(4):602-6. doi: 10.1016/j.bbrc.2008.06.079. Epub 2008 Jun 30.
5
The HSA domain binds nuclear actin-related proteins to regulate chromatin-remodeling ATPases.热稳定抗原(HSA)结构域结合核肌动蛋白相关蛋白以调节染色质重塑ATP酶。
Nat Struct Mol Biol. 2008 May;15(5):469-76. doi: 10.1038/nsmb.1403. Epub 2008 Apr 13.
6
ATP-dependent chromatin remodeling shapes the DNA replication landscape.ATP 依赖的染色质重塑塑造了 DNA 复制格局。
Nat Struct Mol Biol. 2008 May;15(5):477-84. doi: 10.1038/nsmb.1419. Epub 2008 Apr 13.
7
Ino80 chromatin remodeling complex promotes recovery of stalled replication forks.INO80染色质重塑复合物促进停滞复制叉的恢复。
Curr Biol. 2008 Apr 22;18(8):566-75. doi: 10.1016/j.cub.2008.03.049. Epub 2008 Apr 10.
8
INO80 meets a fork in the road.INO80 面临着一个抉择点。
Nat Struct Mol Biol. 2008 Apr;15(4):332-4. doi: 10.1038/nsmb0408-332.
9
The Ino80 chromatin-remodeling enzyme regulates replisome function and stability.INO80染色质重塑酶调节复制体的功能和稳定性。
Nat Struct Mol Biol. 2008 Apr;15(4):338-45. doi: 10.1038/nsmb.1413. Epub 2008 Mar 23.
10
A SWI/SNF- and INO80-dependent nucleosome movement at the INO1 promoter.INO1启动子处依赖SWI/SNF和INO80的核小体移动。
Biochem Biophys Res Commun. 2007 Oct 5;361(4):974-9. doi: 10.1016/j.bbrc.2007.07.109. Epub 2007 Jul 30.

INO80 依赖 ATP 的染色质重塑复合物是核小体间隔因子。

The INO80 ATP-dependent chromatin remodeling complex is a nucleosome spacing factor.

机构信息

Department of Biochemistry and Molecular Biology, Southern Illinois University, Carbondale, IL 62901-4413, USA.

出版信息

Mol Cell Biol. 2011 Feb;31(4):662-73. doi: 10.1128/MCB.01035-10. Epub 2010 Dec 6.

DOI:10.1128/MCB.01035-10
PMID:21135121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3028646/
Abstract

The mobilization of nucleosomes by the ATP-dependent remodeler INO80 is quite different from another remodeler (SWI/SNF) that is also involved in gene activation. Unlike that recently shown for SWI/SNF, INO80 is unable to disassemble nucleosomes when remodeling short nucleosomal arrays. Instead, INO80 more closely resembles, although with notable exceptions, the nucleosome spacing activity of ISW2 and ISW1a, which are generally involved in transcription repression. INO80 required a minimum of 33 to 43 bp of extranucleosomal DNA for mobilizing nucleosomes, with 70 bp being optimal. INO80 prefers to move mononucleosomes to the center of DNA, like ISW2 and ISW1a, but does so with higher precision. Unlike ISW2/1a, INO80 does not require the H4 tail for nucleosome mobilization; instead, the H2A histone tail negatively regulates nucleosome movement by INO80. INO80 moved arrays of two or three nucleosomes with 50 or 79 bp of linker DNA closer together, with a final length of ∼30 bp of linker DNA or a repeat length of ∼177 bp. A minimum length of >30 bp of linker DNA was required for nucleosome movement and spacing by INO80 in arrays.

摘要

INO80 通过 ATP 依赖性重塑酶使核小体动员的方式与另一种参与基因激活的重塑酶(SWI/SNF)截然不同。与最近 SWI/SNF 的研究结果不同,INO80 在重塑短核小体阵列时无法解聚核小体。相反,INO80 更类似于(尽管存在明显的例外)ISW2 和 ISW1a 的核小体间隔活性,而 ISW2 和 ISW1a 通常参与转录抑制。INO80 至少需要 33 到 43 个碱基对的核小体外 DNA 来动员核小体,70 个碱基对是最佳的。INO80 倾向于将单核小体移动到 DNA 的中心,就像 ISW2 和 ISW1a 一样,但它的精确度更高。与 ISW2/1a 不同,INO80 不需要 H4 尾巴来动员核小体;相反,H2A 组蛋白尾巴通过 INO80 负调节核小体运动。INO80 将带有 50 或 79 个碱基对连接 DNA 的两个或三个核小体阵列更紧密地移动在一起,最终连接 DNA 的长度约为 30 个碱基对或重复长度约为 177 个碱基对。INO80 在阵列中移动核小体和间隔需要至少 >30 个碱基对的连接 DNA。