Control of class II gene transcription during in vitro nucleosome assembly.

Suppr

超能文献

作者信息

Workman J L, Taylor I C, Kingston R E, Roeder R G

机构信息

Department of Molecular Biology, Massachusetts General Hospital, Boston 02114.

出版信息

Methods Cell Biol. 1991;35:419-47. doi: 10.1016/s0091-679x(08)60582-8.

DOI:10.1016/s0091-679x(08)60582-8

PMID:1779863

Abstract

摘要

相似文献

Control of class II gene transcription during in vitro nucleosome assembly.

Methods Cell Biol. 1991;35:419-47. doi: 10.1016/s0091-679x(08)60582-8.

Sequence-specific antirepression of histone H1-mediated inhibition of basal RNA polymerase II transcription.

Science. 1991 Feb 8;251(4994):643-9. doi: 10.1126/science.1899487.

Nucleosomes inhibit the initiation of transcription but allow chain elongation with the displacement of histones.核小体抑制转录起始，但允许在组蛋白移位的情况下进行链延伸。

Cell. 1987 Apr 24;49(2):203-10. doi: 10.1016/0092-8674(87)90561-7.

Binding of transcription factor TFIID to the major late promoter during in vitro nucleosome assembly potentiates subsequent initiation by RNA polymerase II.在体外核小体组装过程中转录因子TFIID与主要晚期启动子的结合增强了随后RNA聚合酶II的起始作用。

Cell. 1987 Nov 20;51(4):613-22. doi: 10.1016/0092-8674(87)90130-9.

Chromatin elongation factors.染色质延伸因子

Curr Opin Genet Dev. 2002 Apr;12(2):156-61. doi: 10.1016/s0959-437x(02)00281-2.

The presence of nucleosomes on a DNA template prevents initiation by RNA polymerase II in vitro.DNA模板上核小体的存在会在体外阻止RNA聚合酶II起始转录。

Cell. 1986 Apr 11;45(1):95-104. doi: 10.1016/0092-8674(86)90541-6.

Eukaryotic RNA polymerase II binds to nucleosome cores from transcribed genes.真核生物RNA聚合酶II与转录基因的核小体核心结合。

Nature. 1983 Feb 10;301(5900):482-8. doi: 10.1038/301482a0.

Activation domains of stably bound GAL4 derivatives alleviate repression of promoters by nucleosomes.稳定结合的GAL4衍生物的激活结构域可减轻核小体对启动子的抑制作用。

Cell. 1991 Feb 8;64(3):533-44. doi: 10.1016/0092-8674(91)90237-s.

FACT, a factor that facilitates transcript elongation through nucleosomes.FACT，一种促进转录本通过核小体进行延伸的因子。

Cell. 1998 Jan 9;92(1):105-16. doi: 10.1016/s0092-8674(00)80903-4.

Nucleosome arrays inhibit both initiation and elongation of transcripts by bacteriophage T7 RNA polymerase.核小体阵列抑制噬菌体T7 RNA聚合酶的转录起始和延伸。

J Mol Biol. 1992 Jan 5;223(1):67-78. doi: 10.1016/0022-2836(92)90716-w.

引用本文的文献

Histone H3 Cleavage Assay for Yeast and Chicken Liver H3 Protease.用于酵母和鸡肝H3蛋白酶的组蛋白H3切割分析

Bio Protoc. 2017 Jan 5;7(1):e2085. doi: 10.21769/BioProtoc.2085.

Histone deacetylase 1 activates PU.1 gene transcription through regulating TAF9 deacetylation and transcription factor IID assembly.组蛋白去乙酰化酶1通过调节TAF9去乙酰化和转录因子IID组装来激活PU.1基因转录。

FASEB J. 2017 Sep;31(9):4104-4116. doi: 10.1096/fj.201700022R. Epub 2017 Jun 1.

DNA Physical Properties and Nucleosome Positions Are Major Determinants of HIV-1 Integrase Selectivity.DNA物理性质和核小体位置是HIV-1整合酶选择性的主要决定因素。

PLoS One. 2015 Jun 15;10(6):e0129427. doi: 10.1371/journal.pone.0129427. eCollection 2015.

Intasome architecture and chromatin density modulate retroviral integration into nucleosome.整合体结构和染色质密度调节逆转录病毒整合入核小体的过程。

Retrovirology. 2015 Feb 7;12:13. doi: 10.1186/s12977-015-0145-9.

Histone deacetylase 1 and p300 can directly associate with chromatin and compete for binding in a mutually exclusive manner.组蛋白去乙酰化酶1和p300可直接与染色质结合，并以互斥方式竞争结合。

PLoS One. 2014 Apr 10;9(4):e94523. doi: 10.1371/journal.pone.0094523. eCollection 2014.

Chromatin modification by PSC occurs at one PSC per nucleosome and does not require the acidic patch of histone H2A.PSC 通过单个核小体发生染色质修饰，并且不依赖于组蛋白 H2A 的酸性斑。

PLoS One. 2012;7(10):e47162. doi: 10.1371/journal.pone.0047162. Epub 2012 Oct 11.

Functional coupling between HIV-1 integrase and the SWI/SNF chromatin remodeling complex for efficient in vitro integration into stable nucleosomes.HIV-1 整合酶与 SWI/SNF 染色质重塑复合物之间的功能偶联，有助于体外高效整合到稳定的核小体中。

PLoS Pathog. 2011 Feb 10;7(2):e1001280. doi: 10.1371/journal.ppat.1001280.

Chromatinized templates reveal the requirement for the LEDGF/p75 PWWP domain during HIV-1 integration in vitro.染色质化模板揭示了HIV-1体外整合过程中对LEDGF/p75 PWWP结构域的需求。

Nucleic Acids Res. 2008 Mar;36(4):1237-46. doi: 10.1093/nar/gkm1127. Epub 2008 Jan 3.

Using atomic force microscopy to study chromatin structure and nucleosome remodeling.使用原子力显微镜研究染色质结构和核小体重塑。

Methods. 2007 Mar;41(3):333-41. doi: 10.1016/j.ymeth.2006.08.016.

Role for Nhp6, Gcn5, and the Swi/Snf complex in stimulating formation of the TATA-binding protein-TFIIA-DNA complex.Nhp6、Gcn5和Swi/Snf复合物在刺激TATA结合蛋白-TFIIA-DNA复合物形成中的作用。

Mol Cell Biol. 2004 Sep;24(18):8312-21. doi: 10.1128/MCB.24.18.8312-8321.2004.

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验