Half a century of bacteriophage lambda recombinase: In vitro studies of lambda exonuclease and Red-beta annealase

被引:10
|
作者
Brewster, Jodi L. [1 ,2 ,3 ]
Tolun, Gokhan [1 ,2 ,3 ]
机构
[1] Univ Wollongong, Mol Horizons, Northfields Ave,Bldg 42,Room 111, Keiraville, NSW 2522, Australia
[2] Univ Wollongong, Sch Chem & Mol Biosci, Northfields Ave,Bldg 42,Room 111, Keiraville, NSW 2522, Australia
[3] Illawarra Hlth & Med Res Inst, Wollongong, NSW, Australia
关键词
annealase; exonuclease; phage lambda; Red-beta; single-stranded DNA-binding protein; two-component recombination; DOUBLE-STRANDED DNA; PHAGE-LAMBDA; GENETIC-RECOMBINATION; HOMOLOGOUS RECOMBINATION; LYSOGENIC INDUCTION; DOMAIN-STRUCTURE; PROTEIN; DIGESTION; MECHANISM; BINDING;
D O I
10.1002/iub.2343
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
DNA recombination, replication, and repair are intrinsically interconnected processes. From viruses to humans, they are ubiquitous and essential to all life on Earth. Single-strand annealing homologous DNA recombination is a major mechanism for the repair of double-stranded DNA breaks. An exonuclease and an annealase work in tandem, forming a complex known as a two-component recombinase. Red beta annealase and lambda-exonuclease from phage lambda form the archetypal two-component recombinase complex. In this short review article, we highlight some of thein vitrostudies that have led to our current understanding of the lambda recombinase system. We synthesize insights from more than half a century of research, summarizing the state of our current understanding. From this foundation, we identify the gaps in our knowledge and cast an eye forward to consider what the next 50 years of research may uncover.
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页码:1622 / 1633
页数:12
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