CTD氨酸酸化损害了RNA聚合酶II的终结因子招募
Andreas Mayer1, Martin Heidemann, Michael Lidschreiber
1Gene Center and Department of Biochemistry, Center for Integrated Protein Science Munich, Ludwig-Maximilians-Universität München, Feodor-Lynen-Strasse 25, 81377 Munich, Germany.
概括
的RNA聚合酶II.
科学领域:
- 分子生物学分子生物学
- 基因表达 基因表达
- 生物化学 生物化学
背景情况:
- RNA聚合酶II的C端域 (CTD) 通过招募因子调节转录.
- CTD包括保存的七倍重复.
- CTD酸化模式对于协调转录周期至关重要.
研究的目的:
- 为了研究酵母RNA聚合酶IICTD上的新酸化位点.
- 确定Tyr(1) 酸化在转录过程中对因子招募的功能影响.
- 阐明CTD酸化在协调转录周期阶段中的作用.
主要方法:
- 在酵母中分析酸化RNA聚合酶IICTD.
- 生物化学测定以评估结合CTD的因子.
- 染色体免疫沉以在体内映射酸化模式.
主要成果:
- 酵母RNA聚合酶IICTD除了在其他位点外,在Tyr(1) 处被酸化.
- 酸化增强了延长因子Spt6的结合.
- Tyr(1) 酸化抑制了终结因子Nrd1,Pcf11和Rtt103.3的招募.
- CTD Tyr(1) 酸化在转录过程中受到空间调节,不包括基因体的终结因子.
结论:
- CTD酸化,包括在Tyr(1),作为一个关键的监管机制.
- 不同的酸化模式决定了因子招募和转录周期的进展.
- 一个扩展的CTD代码,基于Tyr{1},Ser{2}和Ser{5}酸化,解释了转录协调.
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