Literature DB >> 2141651

RecA protein reinitiates strand exchange on isolated protein-free DNA intermediates. An ADP-resistant process.

B J Rao1, B Jwang, C M Radding.   

Abstract

Efficient homologous pairing de novo of linear duplex DNA with a circular single strand (plus strand) coated with RecA protein requires saturation and extension of the single strand by the protein. However, strand exchange, the transfer of a strand from duplex DNA to the nucleoprotein filament, which follows homologous pairing, does not require the stable binding of RecA protein to single-stranded DNA. When RecA protein was added back to isolated protein-free DNA intermediates in the presence of sufficient ADP to inhibit strongly the binding of RecA protein to single-stranded DNA, strand exchange nonetheless resumed at the original rate and went to completion. Characterization of the protein-free DNA intermediate suggested that it has a special site or region to which RecA protein binds. Part of the nascent displaced plus strand of the deproteinized intermediate was unavailable as a cofactor for the ATPase activity of RecA protein, and about 30% resisted digestion by P1 endonuclease, which acts preferentially on single-stranded DNA. At the completion of strand exchange, when the distal 5' end of the linear minus strand had been fully incorporated into heteroduplex DNA, a nucleoprotein complex remained that contained all three strands of DNA from which the nascent displaced strand dissociated only over the next 50 to 60 minutes. Deproteinization of this intermediate yielded a complex that also contained three strands of DNA in which the nascent displaced strand was partially resistant to both Escherichia coli exonuclease I and P1 endonuclease. The deproteinized complex showed a broad melting transition between 37 degrees C and temperatures high enough to melt duplex DNA. These results show that strand exchange can be subdivided into two stages: (1) the exchange of base-pairs, which creates a new heteroduplex pair in place of a parental pair; and (2) strand separation, which is the physical displacement of the unpaired strand from the nucleoprotein filament. Between the creation of new heteroduplex DNA and the eventual separation of a third strand, there exists an unusual DNA intermediate that may contain three-stranded regions of natural DNA that are several thousand bases in length.

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Year:  1990        PMID: 2141651     DOI: 10.1016/S0022-2836(05)80264-5

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  11 in total

1.  Torsional stress generated by RecA protein during DNA strand exchange separates strands of a heterologous insert.

Authors:  B Jwang; C M Radding
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-15       Impact factor: 11.205

2.  Stable three-stranded DNA made by RecA protein.

Authors:  B J Rao; M Dutreix; C M Radding
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-15       Impact factor: 11.205

3.  Base pair switching by interconversion of sugar puckers in DNA extended by proteins of RecA-family: a model for homology search in homologous genetic recombination.

Authors:  T Nishinaka; A Shinohara; Y Ito; S Yokoyama; T Shibata
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-15       Impact factor: 11.205

4.  Activities of human recombination protein Rad51.

Authors:  R C Gupta; L R Bazemore; E I Golub; C M Radding
Journal:  Proc Natl Acad Sci U S A       Date:  1997-01-21       Impact factor: 11.205

5.  RuvA and RuvB proteins of Escherichia coli exhibit DNA helicase activity in vitro.

Authors:  I R Tsaneva; B Müller; S C West
Journal:  Proc Natl Acad Sci U S A       Date:  1993-02-15       Impact factor: 11.205

6.  Formation of base triplets by non-Watson-Crick bonds mediates homologous recognition in RecA recombination filaments.

Authors:  B J Rao; C M Radding
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-21       Impact factor: 11.205

7.  Joints formed by RecA protein from oligonucleotides and duplex DNA block initiation and elongation of transcription.

Authors:  E I Golub; D C Ward; C M Radding
Journal:  Nucleic Acids Res       Date:  1992-06-25       Impact factor: 16.971

8.  Genetic recombination in Escherichia coli: Holliday junctions made by RecA protein are resolved by fractionated cell-free extracts.

Authors:  B Connolly; S C West
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

9.  Homologous recognition promoted by RecA protein via non-Watson-Crick bonds between identical DNA strands.

Authors:  B J Rao; C M Radding
Journal:  Proc Natl Acad Sci U S A       Date:  1993-07-15       Impact factor: 11.205

10.  Unusual stability of recombination intermediates made by Escherichia coli RecA protein.

Authors:  B Müller; I Burdett; S C West
Journal:  EMBO J       Date:  1992-07       Impact factor: 11.598

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