通过PARP1的PAR识别调节了DNA依赖的活动,并独立地刺激了PARP1的催化活性
Waghela Deeksha1, Suman Abhishek1, Eerappa Rajakumara1
1Macromolecular Structural Biology Lab, Department of Biotechnology, Indian Institute of Technology Hyderabad, Sangareddy, India.
The FEBS journal
|July 18, 2023
概括
研究人员在Poly ((ADP-ribose) 聚合酶1 (PARP1) 中发现了新的PAR读取器域,这些域与PARylated蛋白结合. 这一发现揭示了其产物PAR.PAR1对PARP1活性的一种全性调节机制.
科学领域:
- 分子生物学分子生物学
- 生物化学 生物化学
- 基因组学就是基因组学.
背景情况:
- 聚ADP-ribosyl化,主要由聚ADP-ribose) 聚合酶1 (PARP1) 进行,对于DNA损伤后的DNA修复至关重要.
- 通过单链 (SSB) 和双链 (DSB) DNA 断裂刺激PARP1活动,但PAR介导的调节尚未得到充分理解.
研究的目的:
- 在 PARP1.1 中识别和描述新的 PAR 阅读器域.
- 为了阐明PARP1活动的PAR介导全调节的机制.
主要方法:
- 蛋白质领域分析分析
- 具有约束力的分析 (竞争具有约束力的研究)
- 酶活性检测试验测定了酶活性.
主要成果:
- 确定ZnF3,BRCT和WGR域为PARylated蛋白质的高亲和度PAR读取器域.
- ZnF1和ZnF2域优先结合到DNA断裂.
- PAR 结合 PARP1 释放 DNA,由 WGR 域促进.
- PAR产品以催化方式刺激PARP1,但抑制了依赖DNA的刺激.
结论:
- 在 PARP1.1 中发现了专门的高亲和度 PAR 阅读器域.
- 发现了一种新的全性调节机制,其中PAR调节了DNA依赖和DNA独立的PARP1活动.
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