Literature DB >> 10506835

Recombinational DNA repair in bacteria and the RecA protein.

M M Cox1.   

Abstract

In bacteria, the major function of homologous genetic recombination is recombinational DNA repair. This is not a process reserved only for rare double-strand breaks caused by ionizing radiation, nor is it limited to situations in which the SOS response has been induced. Recombinational DNA repair in bacteria is closely tied to the cellular replication systems, and it functions to repair damage at stalled replication forks, Studies with a variety of rec mutants, carried out under normal aerobic growth conditions, consistently suggest that at least 10-30% of all replication forks originating at the bacterial origin of replication are halted by DNA damage and must undergo recombinational DNA repair. The actual frequency may be much higher. Recombinational DNA repair is both the most complex and the least understood of bacterial DNA repair processes. When replication forks encounter a DNA lesion or strand break, repair is mediated by an adaptable set of pathways encompassing most of the enzymes involved in DNA metabolism. There are five separate enzymatic processes involved in these repair events: (1) The replication fork assembled at OriC stalls and/or collapses when encountering DNA damage. (2) Recombination enzymes provide a complementary strand for a lesion isolated in a single-strand gap, or reconstruct a branched DNA at the site of a double-strand break. (3) The phi X174-type primosome (or repair primosome) functions in the origin-independent reassembly of the replication fork. (4) The XerCD site-specific recombination system resolves the dimeric chromosomes that are the inevitable by-product of frequent recombination associated with recombinational DNA repair. (5) DNA excision repair and other repair systems eliminate lesions left behind in double-stranded DNA. The RecA protein plays a central role in the recombination phase of the process. Among its many activities, RecA protein is a motor protein, coupling the hydrolysis of ATP to the movement of DNA branches.

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Year:  1999        PMID: 10506835     DOI: 10.1016/s0079-6603(08)60726-6

Source DB:  PubMed          Journal:  Prog Nucleic Acid Res Mol Biol        ISSN: 0079-6603


  77 in total

1.  Crystal structures of Mycobacterium tuberculosis RecA and its complex with ADP-AlF(4): implications for decreased ATPase activity and molecular aggregation.

Authors:  S Datta; M M Prabu; M B Vaze; N Ganesh; N R Chandra; K Muniyappa; M Vijayan
Journal:  Nucleic Acids Res       Date:  2000-12-15       Impact factor: 16.971

2.  An antitumor drug-induced topoisomerase cleavage complex blocks a bacteriophage T4 replication fork in vivo.

Authors:  G Hong; K N Kreuzer
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

3.  Topological testing of the mechanism of homology search promoted by RecA protein.

Authors:  L Cai; U Marquardt; Z Zhang; M J Taisey; J Chen
Journal:  Nucleic Acids Res       Date:  2001-03-15       Impact factor: 16.971

4.  RadA protein from Archaeoglobus fulgidus forms rings, nucleoprotein filaments and catalyses homologous recombination.

Authors:  M J McIlwraith; D R Hall; A Z Stasiak; A Stasiak; D B Wigley; S C West
Journal:  Nucleic Acids Res       Date:  2001-11-15       Impact factor: 16.971

Review 5.  Participation of recombination proteins in rescue of arrested replication forks in UV-irradiated Escherichia coli need not involve recombination.

Authors:  J Courcelle; P C Hanawalt
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

6.  RecA protein promotes the regression of stalled replication forks in vitro.

Authors:  M E Robu; R B Inman; M M Cox
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

Review 7.  Historical overview: searching for replication help in all of the rec places.

Authors:  M M Cox
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

8.  RecA-mediated rescue of Escherichia coli strains with replication forks arrested at the terminus.

Authors:  S Maisnier-Patin; K Nordström; S Dasgupta
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

9.  Characterization of the two Mycobacterium tuberculosis recA promoters.

Authors:  Krishna K Gopaul; Patricia C Brooks; Jean-François Prost; Elaine O Davis
Journal:  J Bacteriol       Date:  2003-10       Impact factor: 3.490

10.  Crystal structures of Mycobacterium smegmatis RecA and its nucleotide complexes.

Authors:  S Datta; R Krishna; N Ganesh; Nagasuma R Chandra; K Muniyappa; M Vijayan
Journal:  J Bacteriol       Date:  2003-07       Impact factor: 3.490

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