Jahan Sanzida, Davie James R
Manitoba Institute of Child Health, University of Manitoba, Winnipeg, Manitoba R3E 3P4 Canada.
Manitoba Institute of Child Health, University of Manitoba, Winnipeg, Manitoba R3E 3P4 Canada.
Adv Biol Regul. 2015 Jan;57:173-84. doi: 10.1016/j.jbior.2014.09.003. Epub 2014 Sep 17.
The mammalian genome encodes eleven protein arginine methyltransferases (PRMTs) that are involved in the transfer of a methyl group from S-adenosylmethionine (AdoMet) to the guanidino nitrogen of arginine. The substrates for these enzymes range from histones to several nuclear and cytoplasmic proteins. Methylation of histones by PRMTs can block the docking site for other reader/effector molecules and thus this modification can interfere with histone code orchestration. Several members of the PRMTs have roles in chromatin organization and function. Although PRMT aberrant expression is correlated with several diseases including cancer, the underlying mechanisms are still obscure in most cases.
哺乳动物基因组编码11种蛋白质精氨酸甲基转移酶(PRMT),这些酶参与将甲基从S-腺苷甲硫氨酸(AdoMet)转移至精氨酸的胍基氮上。这些酶的底物范围从组蛋白到多种核蛋白和胞质蛋白。PRMT介导的组蛋白甲基化可阻断其他读取器/效应分子的对接位点,因此这种修饰会干扰组蛋白编码编排。PRMT的几个成员在染色质组织和功能中发挥作用。尽管PRMT异常表达与包括癌症在内的多种疾病相关,但在大多数情况下其潜在机制仍不清楚。