Kedar Padmini S, Kim Soon-Jong, Robertson Anthony, Hou Esther, Prasad Rajendra, Horton Julie K, Wilson Samuel H
Laboratory of Structural Biology, NIEHS/National Institutes of Health, 111 T.W. Alexander Drive, Research Triangle Park, NC 27709, USA.
J Biol Chem. 2002 Aug 23;277(34):31115-23. doi: 10.1074/jbc.M201497200. Epub 2002 Jun 12.
Proliferating cell nuclear antigen (PCNA) plays an essential role in nucleic acid metabolism as a component of the DNA replication and DNA repair machinery. As such, PCNA interacts with many proteins that have a sequence motif termed the PCNA interacting motif (PIM) and also with proteins lacking a PIM. Three regions in human and rat DNA polymerases beta (beta-pol) that resemble the consensus PIM were identified, and we show here that beta-polymerase and PCNA can form a complex both in vitro and in vivo. Immunoprecipitation experiments, yeast two-hybrid analysis, and overlay binding assays were used to examine the interaction between the two proteins. Competition experiments with synthetic PIM-containing peptides suggested the importance of a PIM in the interaction, and studies of a beta-polymerase PIM mutant, H222A/F223A, demonstrated that this alteration blocked the interaction with PCNA. The results indicate that at least one of the PIM-like sequences in beta-polymerase appears to be a functional PIM and was required in the interaction between beta-polymerase and PCNA.
增殖细胞核抗原(PCNA)作为DNA复制和DNA修复机制的一个组成部分,在核酸代谢中起着至关重要的作用。因此,PCNA与许多具有称为PCNA相互作用基序(PIM)的序列基序的蛋白质相互作用,也与缺乏PIM的蛋白质相互作用。在人和大鼠DNA聚合酶β(β-pol)中鉴定出了三个类似于共有PIM的区域,我们在此表明β-聚合酶和PCNA在体外和体内都能形成复合物。免疫沉淀实验、酵母双杂交分析和覆盖结合试验用于检测这两种蛋白质之间的相互作用。用含合成PIM的肽进行的竞争实验表明PIM在相互作用中的重要性,对β-聚合酶PIM突变体H222A/F223A的研究表明,这种改变阻断了与PCNA的相互作用。结果表明,β-聚合酶中至少一个类PIM序列似乎是一个功能性PIM,是β-聚合酶与PCNA相互作用所必需的。