转录合的H3K36三甲基化由Set2在与FACT协调的结构基础
Tomoya Kujirai1,2, Haruhiko Ehara2, Tomoko Ito1
1Laboratory of Chromatin Structure and Function, Institute for Quantitative Biosciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
基因组H3K36三甲基化 (H3K36me3) 确保了转录的准确性. 这项研究揭示了Set2酶针对RNA聚合酶II延长复合体背后的核细胞重组,由Spt6指导,以沉积H3K36me3.3.
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.
- 染色体生物学 染色体生物学
背景情况:
- 在H3K36 (H3K36me3) 的基因组三甲基化对转录忠实性至关重要.
- 这种修饰是由Set2在RNA聚合酶II延伸复合体 (EC) 的转录延伸过程中催化.
研究的目的:
- 为了阐明转录合H3K36me3沉积的机制.
- 了解Set2与EC和核细胞相互作用的结构基础.
主要方法:
- 低温电子显微镜 (cryo-EM) 用于确定结构复杂.
- 生物化学测试用于研究酶-核酶相互作用.
主要成果:
- 通过set2介导的H3K36me3沉积发生在核细胞体上,核细胞体在EC后面重组.
- 基因组辅导体FACT抑制H3K36me3在下游核细胞体上,确保Set2准上游核细胞体.
- 低温EM结构显示,Set2被EC的Spt6子单元定,逐步捕获H3的N端尾部.
- 破坏Set2-EC相互作用会影响转录合的H3K36me3沉积.
结论:
- 阐明了转录合H3K36me3沉积的基于结构的机制.
- Set2的精确准确保了H3K36me3沉积在重组核细胞上,保持了转录的真实性.
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