在活细胞中连接染色体化标记定义的蛋白质和基因组
Fangfei Qin1, Boyuan Li2, Hui Wang2
1Synthetic and Functional Biomolecules Center, Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China; Peking-Tsinghua Center for Life Sciences, Academy of Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China; Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China; Shenzhen Bay Laboratory, Shenzhen 518055, China.
我们开发了一种新的SiTomics策略, 这种方法将代谢物与染色质变化联系起来,揭示了基因调节和蛋白质相互作用的新见解.
科学领域:
- 生物化学
- 分子生物学
- 表观遗传学
背景情况:
- 在活细胞中绘制动态基因组修饰具有挑战性.
- 需要一个可通用的,特定于特定地点的 chromatin 分析策略.
研究的目的:
- 开发一个单位解决的多组学 (SiTomics) 策略,用于绘制动态基因组修饰.
- 在活细胞中通过特定的染色体化定义的染色体和基因组.
主要方法:
- 通过利用基因代码扩展来开发SiTomics工具包.
- 用短链脂肪酸刺激细胞观察基因组的变化.
- 整合多组数据,将修改与蛋白质组,基因组和功能联系起来.
主要成果:
- 在刺激时显现出明显的化 (H3K56cr) 和β-化 (H3K56bhb).
- 确定GLYR1是一种调节H3K56cr定位的蛋白质.
- 发现与β-基化相关的超强增强剂.
结论:
- SiTomics可以系统地绘制动态修饰和染色体概况.
- 建立了染色体化标记,蛋白质组,基因组和细胞功能之间的联系.
- SiTomics是一个用于剖析基因组以外的"代谢物-修饰-调节"轴的平台.
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