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聚腺苷酸化核糖基化在DNA损伤修复途径中的功能。

Functions of PARylation in DNA Damage Repair Pathways.

作者信息

Wei Huiting, Yu Xiaochun

机构信息

Department of Immunology, Tianjin Key Laboratory of Cellular and Molecular Immunology, MOE Key Laboratory of Immune Microenvironment and Disease, School of Basic Medical Sciences, Tianjin Medical University, Tianjin 300070, China.

Department of Cancer Genetics and Epigenetics, Beckman Research Institute, City of Hope Medical Center, Duarte, CA 91010, USA.

出版信息

Genomics Proteomics Bioinformatics. 2016 Jun;14(3):131-139. doi: 10.1016/j.gpb.2016.05.001. Epub 2016 May 27.

Abstract

Protein poly ADP-ribosylation (PARylation) is a widespread post-translational modification at DNA lesions, which is catalyzed by poly(ADP-ribose) polymerases (PARPs). This modification regulates a number of biological processes including chromatin reorganization, DNA damage response (DDR), transcriptional regulation, apoptosis, and mitosis. PARP1, functioning as a DNA damage sensor, can be activated by DNA lesions, forming PAR chains that serve as a docking platform for DNA repair factors with high biochemical complexity. Here, we highlight molecular insights into PARylation recognition, the expanding role of PARylation in DDR pathways, and the functional interaction between PARylation and ubiquitination, which will offer us a better understanding of the biological roles of this unique post-translational modification.

摘要

蛋白质聚ADP-核糖基化(PARylation)是DNA损伤处广泛存在的一种翻译后修饰,由聚(ADP-核糖)聚合酶(PARP)催化。这种修饰调节许多生物学过程,包括染色质重组、DNA损伤反应(DDR)、转录调控、细胞凋亡和有丝分裂。PARP1作为一种DNA损伤传感器,可被DNA损伤激活,形成PAR链,作为具有高生化复杂性的DNA修复因子的对接平台。在这里,我们重点介绍对PARylation识别的分子见解、PARylation在DDR途径中不断扩展的作用以及PARylation与泛素化之间的功能相互作用,这将有助于我们更好地理解这种独特翻译后修饰的生物学作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818c/4936651/9d2c3405acd0/gr1.jpg

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