Literature DB >> 13678587

A molecular throttle: the recombination hotspot chi controls DNA translocation by the RecBCD helicase.

Maria Spies1, Piero R Bianco, Mark S Dillingham, Naofumi Handa, Ronald J Baskin, Stephen C Kowalczykowski.   

Abstract

RecBCD enzyme is a heterotrimeric helicase/nuclease that initiates homologous recombination at double-stranded DNA breaks. Several of its activities are regulated by the DNA sequence chi (5'-GCTGGTGG-3'), which is recognized in cis by the translocating enzyme. When RecBCD enzyme encounters chi, the intensity and polarity of its nuclease activity are changed, and the enzyme gains the ability to load RecA protein onto the chi-containing, unwound single-stranded DNA. Here, we show that interaction with chi also affects translocation by RecBCD enzyme. By observing translocation of individual enzymes along single molecules of DNA, we could see RecBCD enzyme pause precisely at chi. Furthermore, and more unexpectedly, after pausing at chi, the enzyme continues translocating but at approximately one-half the initial rate. We propose that interaction with chi results in an enzyme in which one of the two motor subunits, likely the RecD motor, is uncoupled from the holoenzyme to produce the slower translocase.

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Year:  2003        PMID: 13678587     DOI: 10.1016/s0092-8674(03)00681-0

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  86 in total

Review 1.  Multiple pathways process stalled replication forks.

Authors:  Bénédicte Michel; Gianfranco Grompone; Maria-Jose Florès; Vladimir Bidnenko
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-24       Impact factor: 11.205

2.  Forward and reverse motion of single RecBCD molecules on DNA.

Authors:  Thomas T Perkins; Hung-Wen Li; Ravindra V Dalal; Jeff Gelles; Steven M Block
Journal:  Biophys J       Date:  2004-03       Impact factor: 4.033

Review 3.  How RecBCD enzyme and Chi promote DNA break repair and recombination: a molecular biologist's view.

Authors:  Gerald R Smith
Journal:  Microbiol Mol Biol Rev       Date:  2012-06       Impact factor: 11.056

4.  Alteration of χ recognition by RecBCD reveals a regulated molecular latch and suggests a channel-bypass mechanism for biological control.

Authors:  Liang Yang; Naofumi Handa; Bian Liu; Mark S Dillingham; Dale B Wigley; Stephen C Kowalczykowski
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-17       Impact factor: 11.205

5.  PcrA helicase dismantles RecA filaments by reeling in DNA in uniform steps.

Authors:  Jeehae Park; Sua Myong; Anita Niedziela-Majka; Kyung Suk Lee; Jin Yu; Timothy M Lohman; Taekjip Ha
Journal:  Cell       Date:  2010-08-20       Impact factor: 41.582

6.  Single-molecule visualization of RecQ helicase reveals DNA melting, nucleation, and assembly are required for processive DNA unwinding.

Authors:  Behzad Rad; Anthony L Forget; Ronald J Baskin; Stephen C Kowalczykowski
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-04       Impact factor: 11.205

7.  Recombination hotspots attenuate the coupled ATPase and translocase activities of an AddAB-type helicase-nuclease.

Authors:  Neville S Gilhooly; Mark S Dillingham
Journal:  Nucleic Acids Res       Date:  2014-03-15       Impact factor: 16.971

8.  Effects of recJ, recQ, and recFOR mutations on recombination in nuclease-deficient recB recD double mutants of Escherichia coli.

Authors:  Ivana Ivancic-Bace; Erika Salaj-Smic; Krunoslav Brcic-Kostic
Journal:  J Bacteriol       Date:  2005-02       Impact factor: 3.490

9.  The P. furiosus mre11/rad50 complex promotes 5' strand resection at a DNA double-strand break.

Authors:  Ben B Hopkins; Tanya T Paull
Journal:  Cell       Date:  2008-10-17       Impact factor: 41.582

10.  Specific inhibition of the E.coli RecBCD enzyme by Chi sequences in single-stranded oligodeoxyribonucleotides.

Authors:  Avanti Kulkarni; Douglas A Julin
Journal:  Nucleic Acids Res       Date:  2004-07-14       Impact factor: 16.971

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