Coordination of multiple enzyme activities by a single PCNA in archaeal Okazaki fragment maturation

被引:49
作者
Beattie, Thomas R. [1 ]
Bell, Stephen D. [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
archaea; DNA replication; Okazaki fragment; PCNA; DNA-BINDING-PROTEIN; SULFOLOBUS-SOLFATARICUS; SLIDING-CLAMP; HETEROTRIMERIC PCNA; REPLICATION FORK; PRIMER REMOVAL; STRUCTURAL BASIS; POLYMERASE; COMPLEX; FEN1;
D O I
10.1038/emboj.2012.12
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
Chromosomal DNA replication requires one daughter strand-the lagging strand-to be synthesised as a series of discontinuous, RNA-primed Okazaki fragments, which must subsequently be matured into a single covalent DNA strand. Here, we describe the reconstitution of Okazaki fragment maturation in vitro using proteins derived from the archaeon Sulfolobus solfataricus. Six proteins are necessary and sufficient for coupled DNA synthesis, RNA primer removal and DNA ligation. PolB1, Fen1 and Lig1 provide the required catalytic activities, with coordination of their activities dependent upon the DNA sliding clamp, proliferating cell nuclear antigen (PCNA). S. solfataricus PCNA is a heterotrimer, with each subunit having a distinct specificity for binding PolB1, Fen1 or Lig1. Our data demonstrate that the most efficient coupling of activities occurs when a single PCNA ring organises PolB1, Fen1 and Lig1 into a complex. The EMBO Journal (2012) 31, 1556-1567. doi:10.1038/emboj.2012.12; Published online 3 February 2012
引用
收藏
页码:1556 / 1567
页数:12
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