PRC1无处不在模块的晶体结构与核细胞组结合在一起
Robert K McGinty1, Ryan C Henrici2, Song Tan1
1Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Nature
|October 31, 2014
概括
聚合物抑制复合物1 (PRC1) 使用其E3-E2酶复合物来无处不在的基因组H2A. 晶体结构揭示了PRC1如何通过与催化部位不同的相互作用来识别核酶体基质.
科学领域:
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 分子生物学分子生物学
- 结构生物学 结构生物学
背景情况:
- 多组 (PcG) 蛋白质是重要的表观遗传调节剂.
- PRC1复合物无处不在地基因组 H2A Lys119,影响基因表达.
- 通过PRC1识别核细胞的机制仍然是难以捉摸的.
研究的目的:
- 通过PRC1.1.阐明核细胞基质识别的分子机制.
- 确定PRC1无处不在活动的结构基础.
主要方法:
- 在X射线晶体学.
- 生物化学测定 (隐含)
主要成果:
- 人类Ring1B-Bmi1-UbcH5c E3-E2复合物的晶体结构与核素核粒子结合.
- 通过与多个核酶体表面的相互作用来识别基质识别.
- 揭示了E2酶 (UbcH5c) 在基质结合中的新型作用.
结论:
- PRC1通过远离催化部位的相互作用来实现基质特异性.
- E2酶在核细胞识别中起着意想不到的作用.
- 结构洞察力有助于了解像BRCA1.1这样的相关酶.
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