素H2B单双化功能与FACT合作,以调节RNA聚合酶II的延长
Rushad Pavri1, Bing Zhu, Guohong Li
1Howard Hughes Medical Institute, Department of Biochemistry, Division of Nucleic Acids Enzymology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, 683 Hoes Lane, Piscataway, NJ 08854, USA.
Cell
|May 23, 2006
概括
转录活动的标记物 - - 基因组H2B单双基因化 - - 由RNF20/40和UbcH6.6确定. 这个过程需要转录因子,通过染色质促进RNA聚合酶II的延长.
科学领域:
- 分子生物学分子生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 基因规则 基因规则
背景情况:
- 基因组转化后修改通过改变染色质结构来调节基因表达.
- 基因组H2B单双化与活跃转录有关,但其在延长中的建立和作用尚未完全理解.
研究的目的:
- 为了研究建立基质子H2B单双化的分子机制.
- 阐明H2B单双化在RNA聚合酶II转录延长中的作用.
主要方法:
- 使用了与可诱导的促进子重组的染色体转录系统.
- 在体外和体内实验中用于分析蛋白质-DNA相互作用和转录生成.
主要成果:
- 基因组H2B单双化建立取决于转录,PAF复合体和FACT伴侣.
- H2B单双化增强了FACT功能,促进了转录延长和更长的RNA合成.
- 通过核体延长RNA聚合酶II最小需要FACT和招募PAF和H2B单双化机械.
结论:
- 基因组H2B单双化是一种转录依赖的过程,对于高效的转录延长至关重要.
- FACT复合体和PAF/H2B单双化机制是RNA聚合酶II通过核体的关键调节者.
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