Chuang L S, Ian H I, Koh T W, Ng H H, Xu G, Li B F
Chemical Carcinogenesis Laboratory, Institute of Molecular and Cell Biology, National University of Singapore, Kent Ridge Crescent, Singapore 119260, Republic of Singapore.
Science. 1997 Sep 26;277(5334):1996-2000. doi: 10.1126/science.277.5334.1996.
DNA-(cytosine-5) methyltransferase (MCMT) methylates newly replicated mammalian DNA, but the factors regulating this activity are unknown. Here, MCMT is shown to bind proliferating cell nuclear antigen (PCNA), an auxiliary factor for DNA replication and repair. Binding of PCNA requires amino acids 163 to 174 of MCMT, occurs in intact cells at foci of newly replicated DNA, and does not alter MCMT activity. A peptide derived from the cell cycle regulator p21(WAF1) can disrupt the MCMT-PCNA interaction, which suggests that p21(WAF1) may regulate methylation by blocking access of MCMT to PCNA. MCMT and p21(WAF1) may be linked in a regulatory pathway, because the extents of their expression are inversely related in both SV40-transformed and nontransformed cells.
DNA(胞嘧啶-5)甲基转移酶(MCMT)可使新复制的哺乳动物DNA发生甲基化,但调节这种活性的因素尚不清楚。本文表明,MCMT可与增殖细胞核抗原(PCNA)结合,PCNA是DNA复制和修复的辅助因子。PCNA的结合需要MCMT的163至174位氨基酸,在完整细胞中新复制DNA的位点发生,且不改变MCMT的活性。源自细胞周期调节因子p21(WAF1)的肽可破坏MCMT与PCNA的相互作用,这表明p21(WAF1)可能通过阻止MCMT与PCNA结合来调节甲基化。MCMT和p21(WAF1)可能在一条调节途径中相关联,因为在SV40转化细胞和未转化细胞中它们的表达程度呈负相关。