Literature DB >> 11340628

Therefore, what are recombination proteins there for?

J Courcelle1, A K Ganesan, P C Hanawalt.   

Abstract

The order of discovery can have a profound effect upon the way in which we think about the function of a gene. In E. coli, recA is nearly essential for cell survival in the presence of DNA damage. However, recA was originally identified, as a gene required to obtain recombinant DNA molecules in conjugating bacteria. As a result, it has been frequently assumed that recA promotes the survival of bacteria containing DNA damage by recombination in which DNA strand exchanges occur. We now know that several of the processes that interact with or are controlled by recA, such as excision repair and translesion synthesis, operate to ensure that DNA replication occurs processively without strand exchanges. Yet the view persists in the literature that recA functions primarily to promote recombination during DNA repair. With the benefit of hindsight and more than three decades of additional research, we reexamine some of the classical experiments that established the concept of DNA repair by recombination, and we consider the possibilities that recombination is not an efficient mechanism for rescuing damaged cells, and that recA may be important for maintaining processive replication in a manner that does not generally promote recombination. Copyright 2001 John Wiley & Sons, Inc.

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Year:  2001        PMID: 11340628     DOI: 10.1002/bies.1065

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  31 in total

Review 1.  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

2.  Associations between inverted repeats and the structural evolution of bacterial genomes.

Authors:  Guillaume Achaz; Eric Coissac; Pierre Netter; Eduardo P C Rocha
Journal:  Genetics       Date:  2003-08       Impact factor: 4.562

3.  RuvAB and RecG are not essential for the recovery of DNA synthesis following UV-induced DNA damage in Escherichia coli.

Authors:  Janet R Donaldson; Charmain T Courcelle; Justin Courcelle
Journal:  Genetics       Date:  2004-04       Impact factor: 4.562

4.  Ring-shaped architecture of RecR: implications for its role in homologous recombinational DNA repair.

Authors:  Byung Il Lee; Kyoung Hoon Kim; Soo Jeong Park; Soo Hyun Eom; Hyun Kyu Song; Se Won Suh
Journal:  EMBO J       Date:  2004-04-29       Impact factor: 11.598

5.  Genetic recombination in Bacillus subtilis 168: contribution of Holliday junction processing functions in chromosome segregation.

Authors:  Begoña Carrasco; M Castillo Cozar; Rudi Lurz; Juan C Alonso; Silvia Ayora
Journal:  J Bacteriol       Date:  2004-09       Impact factor: 3.490

6.  Nucleotide excision repair or polymerase V-mediated lesion bypass can act to restore UV-arrested replication forks in Escherichia coli.

Authors:  Charmain T Courcelle; Jerilyn J Belle; Justin Courcelle
Journal:  J Bacteriol       Date:  2005-10       Impact factor: 3.490

7.  A complementary pair of rapid molecular screening assays for RecA activities.

Authors:  Andrew M Lee; Tim J Wigle; Scott F Singleton
Journal:  Anal Biochem       Date:  2007-04-20       Impact factor: 3.365

8.  UvrD303, a hyperhelicase mutant that antagonizes RecA-dependent SOS expression by a mechanism that depends on its C terminus.

Authors:  Richard C Centore; Michael C Leeson; Steven J Sandler
Journal:  J Bacteriol       Date:  2008-12-12       Impact factor: 3.490

9.  Double-strand break repair pathways protect against CAG/CTG repeat expansions, contractions and repeat-mediated chromosomal fragility in Saccharomyces cerevisiae.

Authors:  Rangapriya Sundararajan; Lionel Gellon; Rachel M Zunder; Catherine H Freudenreich
Journal:  Genetics       Date:  2009-11-09       Impact factor: 4.562

10.  The Rtt109 histone acetyltransferase facilitates error-free replication to prevent CAG/CTG repeat contractions.

Authors:  Jiahui H Yang; Catherine H Freudenreich
Journal:  DNA Repair (Amst)       Date:  2010-01-18
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