Thompson Paul R, Fast Walter
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina 29208, USA.
ACS Chem Biol. 2006 Aug 22;1(7):433-41. doi: 10.1021/cb6002306.
Protein citrullination, a once-obscure post-translational modification (PTM) of peptidylarginine, has recently become an area of significant interest because of its suspected role in human disease states, including rheumatoid arthritis and multiple sclerosis, and also because of its newfound role in gene regulation. One protein isozyme responsible for this modification, protein arginine deiminase 4 (PAD4), has also been proposed to "reverse" epigenetic histone modifications made by the protein arginine methyltransferases. Here, we review the in vivo and in vitro studies of transcriptional regulation by PAD4, evaluate conflicting evidence for its ability to use methylated peptidylarginine as a substrate, and highlight promising areas of future work. Understanding the interplay of multiple arginine PTMs is an emerging area of importance in health and disease and is a topic best addressed by novel tools in proteomics and chemical biology.
蛋白质瓜氨酸化是肽基精氨酸一种曾经鲜为人知的翻译后修饰(PTM),由于其在包括类风湿性关节炎和多发性硬化症在内的人类疾病状态中可能发挥的作用,以及在基因调控方面新发现的作用,最近已成为一个备受关注的领域。一种负责这种修饰的蛋白质同工酶,即蛋白质精氨酸脱亚氨酶4(PAD4),也被认为可以“逆转”由蛋白质精氨酸甲基转移酶进行的表观遗传组蛋白修饰。在这里,我们回顾了PAD4对转录调控的体内和体外研究,评估了其将甲基化肽基精氨酸用作底物能力的相互矛盾的证据,并强调了未来工作中前景广阔的领域。了解多种精氨酸PTM之间的相互作用是健康与疾病领域一个新出现的重要领域,也是蛋白质组学和化学生物学中的新工具最适合解决的一个话题。