Dynamic elements of replication protein A at the crossroads of DNA replication, recombination, and repair

被引:61
|
作者
Caldwell, Colleen C. [1 ]
Spies, Maria [1 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Biochem, 451 Newton Rd, Iowa City, IA 52242 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Conformational protein dynamics; replication protein A (RPA); DNA replication; DNA repair; homologous recombination; protein-DNA interctions; single-molecule; SINGLE-STRANDED-DNA; 70 KDA SUBUNIT; BINDING-PROTEIN; SACCHAROMYCES-CEREVISIAE; T-ANTIGEN; ATAXIA-TELANGIECTASIA; CHECKPOINT RESPONSE; RPA PHOSPHORYLATION; FUNCTIONAL-ANALYSIS; UNWINDING ACTIVITY;
D O I
10.1080/10409238.2020.1813070
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
The heterotrimeric eukaryotic Replication protein A (RPA) is a master regulator of numerous DNA metabolic processes. For a long time, it has been viewed as an inert protector of ssDNA and a platform for assembly of various genome maintenance and signaling machines. Later, the modular organization of the RPA DNA binding domains suggested a possibility for dynamic interaction with ssDNA. This modular organization has inspired several models for the RPA-ssDNA interaction that aimed to explain how RPA, the high-affinity ssDNA binding protein, is replaced by the downstream players in DNA replication, recombination, and repair that bind ssDNA with much lower affinity. Recent studies, and in particular single-molecule observations of RPA-ssDNA interactions, led to the development of a new model for the ssDNA handoff from RPA to a specific downstream factor where not only stability and structural rearrangements but also RPA conformational dynamics guide the ssDNA handoff. Here we will review the current knowledge of the RPA structure, its dynamic interaction with ssDNA, and how RPA conformational dynamics may be influenced by posttranslational modification and proteins that interact with RPA, as well as how RPA dynamics may be harnessed in cellular decision making.
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页码:482 / 507
页数:26
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