Department of Physiological Chemistry, LMU BioMedical Center, Faculty of Medicine, Ludwig Maximilians University of Munich, Butenandtstrasse 5B, 81377 Munich, Germany.
Curr Opin Struct Biol. 2012 Dec;22(6):721-9. doi: 10.1016/j.sbi.2012.08.005. Epub 2012 Sep 15.
ADP-ribosylation is a post-translational modification of proteins that occurs mostly in response to cellular stress and is catalysed by members of the diverse poly-ADP-ribose (PAR) polymerase (PARP/ARTD) family. The founding member of the family, PARP1, is best recognized for its function as a sensor of DNA strand lesions, but ADP-ribosylation has been implicated in transcriptional regulation, chromatin dynamics, telomere maintenance, apoptosis and neuronal signalling. Here we summarize a number of exciting recent breakthroughs in our understanding of the structural and mechanistic aspects of how PARP1 recognizes DNA, how PARPs are regulated, how ADP-ribose modifications are set onto specific targets and how the cellular machinery recognizes this elusive post-translational modification.
ADP-核糖基化是一种蛋白质的翻译后修饰,主要发生在细胞应激响应时,由多聚 ADP-核糖聚合酶 (PARP/ARTD) 家族成员催化。该家族的创始成员 PARP1 作为 DNA 链损伤的传感器而广为人知,但 ADP-核糖基化已被牵涉到转录调控、染色质动力学、端粒维持、细胞凋亡和神经元信号转导中。在此,我们总结了在理解 PARP1 如何识别 DNA、PARPs 如何被调控、ADP-核糖基修饰如何被施加到特定靶标以及细胞机制如何识别这种难以捉摸的翻译后修饰等方面的一些激动人心的最新突破。