RecA-dependent recovery of arrested DNA replication forks

被引:165
作者
Courcelle, J
Hanawalt, PC
机构
[1] Mississippi State Univ, Dept Biol Sci, Mississippi State, MS 39762 USA
[2] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
关键词
RecA; replication; repair; DNA damage; recombination;
D O I
10.1146/annurev.genet.37.110801.142616
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
DNA damage encountered during the cellular process of chromosomal replication can disrupt the replication machinery and result in mutagenesis or lethality. The RecA protein of Escherichia coli is essential for survival in this situation: It maintains the integrity of the arrested replication fork and signals the upregulation of over 40 gene products, of which most are required to restore the genomic template and to facilitate the resumption of processive replication. Although RecA was originally discovered as a gene product that was required to change the genetic information during sexual cell cycles, over three decades of research have revealed that it is also the key enzyme required to maintain the genetic information when DNA damage is encountered during replication in asexual cell cycles. In this review, we examine the significant experimental approaches that have led to our current understanding of the RecA-mediated processes that restore replication following encounters with DNA damage.
引用
收藏
页码:611 / 646
页数:36
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