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在HDAC6-RNF168轴调节H2A/H2A.X无处不在,使双链断裂修复
Lingyu Qiu1, Wenchao Xu1, Xiaopeng Lu1
1International Cancer Center, Guangdong Key Laboratory of Genome Instability and Human Disease Prevention, Marshall Laboratory of Biomedical Engineering, Department of Biochemistry and Molecular Biology, Shenzhen University Medical School, Shenzhen 518055, China.
Nucleic acids research
|July 28, 2023
概括
基因组脱乙酶6 (HDAC6) 负面调节DNA双链断裂 (DSB) 修复. 这涉及HDAC6降解,促进修复因子招募和DNA修复,提供潜在的癌症治疗策略.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 癌症研究 癌症研究
背景情况:
- 已知基因组脱乙酶6 (HDAC6) 能调节DNA损伤信号通路.
- 它在DNA双链断裂 (DSB) 修复中的作用仍然在很大程度上未被描述.
研究的目的:
- 研究HDAC6在DNA双链断裂 (DSB) 修复中的作用.
- 阐明HDAC6影响DSB修复的分子机制.
主要方法:
- 细胞测试检查蛋白质相互作用和局部化.
- 乌比基化和蛋白质体降解研究.
- 评估DNA修复因子的招募和DNA修复效率.
主要成果:
- HDAC6以一种独立于酶活性的方式负面调节DSB修复.
- HDAC6 阻止了 RNF168 在未受压力的细胞中使 H2A/H2A.X 无处不在.
- DSBs触发了RNF168介导的HDAC6的泛化和降解,促进了H2A/H2A.X泛化和像53BP1和BRCA1.1这样的修复因子的招募.
结论:
- 一个新的HDAC6-RNF168调节轴控制H2A/H2A.X无处不在状态.
- 这个轴对于高效的DSB维修至关重要.
- 准这一轴可以克服癌细胞对基因毒性损伤的抵抗力,从而提出一种潜在的治疗策略.
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