Dual mode of interaction of DNA polymerase ε with proliferating cell nuclear antigen in primer binding and DNA synthesis

被引:24
作者
Maga, G
Jónsson, ZO
Stucki, M
Spadari, S
Hübscher, U
机构
[1] CNR, Inst Biochem & Evolut Genet, IGBE, I-27100 Pavia, Italy
[2] Univ Zurich Irchel, Inst Vet Biochem, CH-8057 Zurich, Switzerland
关键词
DNA replication; DNA polymerase; processivity factor; protein-protein interaction; PCNA mutagenesis;
D O I
10.1006/jmbi.1998.2314
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proliferating cell nuclear antigen can interact with DNA polymerase epsilon on linear DNA templates, even in the absence of other auxiliary factors (replication factor C, replication protein A), and thereby stimulate its primer recognition and DNA synthesis. Using four characterized mutants of proliferating cell nuclear antigen containing three or four alanine residue substitutions on the C-terminal side and the back side of the trimer, we have tested the kinetics of primer binding and nucleotide incorporation by DNA polymerase epsilon in different assays. In contrast with what has been found in interaction studies between DNA polymerase delta and proliferating cell nuclear antigen, our data suggested that stimulation of DNA polymerase epsilon primer binding involves interactions with both the C-terminal side and the back side of proliferating cell nuclear antigen. However, for stimulation of DNA polymerase epsilon DNA synthesis, exclusively the C-terminal side appears to be sufficient. The significance of this dual interaction is discussed with reference to the physiological roles of DNA polymerase epsilon and its interaction with the clamp proliferating cell nuclear antigen. (C) 1999 Academic Press.
引用
收藏
页码:259 / 267
页数:9
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