Literature DB >> 2993796

Recombination in the lambda repressor gene: evidence that very short patch (VSP) mismatch correction restores a specific sequence.

M Lieb.   

Abstract

The mutation am6 in the cI gene of bacteriophage lambda is identified as a C----T transition in a 5'CCATGG sequence. In four-factor crosses of am6 with nearby mutations in cI, the frequencies of cI+ recombinants are much higher than expected from the physical distances. A very short patch (VSP) mismatch repair system is presumed to recognize am6/am+ mispairs in the heteroduplexes that accompany recombination between the outside markers. Mutation am6 is corrected to am+; correction of am+ to am6 was not detected. Clear-plaque mutation 1-1 in cI is a T----C transition in a 5'CTTGG sequence, resulting in the sequence 5'CCATGG. When 1-1 was crossed with nearby mutations in gene cI, there were no excess cI+ recombinants, which would result from repair of CCTGG (1-1) to CTTGG (cI+). However, in crosses of cI+ phages with mutation 1-1, there was an excess of cI- recombinants, indicating that cI+ was repaired to 1-1. Preferential repair does not require adenine or cytosine methylation: when repairing a mismatch, the VSP repair system apparently identifies specific mispaired bases by sequence alone.

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Year:  1985        PMID: 2993796     DOI: 10.1007/bf00330759

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  23 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1976-11       Impact factor: 11.205

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Journal:  J Mol Biol       Date:  1977-07       Impact factor: 5.469

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Journal:  Annu Rev Genet       Date:  1978       Impact factor: 16.830

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Journal:  Proc Natl Acad Sci U S A       Date:  1966-02       Impact factor: 11.205

6.  A fine structure map of spontaneous and induced mutations in the lambda repressor gene, including insertions of IS elements.

Authors:  M Lieb
Journal:  Mol Gen Genet       Date:  1981

7.  A plasmid cloning vehicle allowing a positive selection for inserted fragments.

Authors:  T M Roberts; S L Swanberg; A Poteete; G Riedel; K Backman
Journal:  Gene       Date:  1980-12       Impact factor: 3.688

8.  Mismatch repair in Streptococcus pneumoniae: relationship between base mismatches and transformation efficiencies.

Authors:  J P Claverys; V Méjean; A M Gasc; A M Sicard
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

9.  Hyperrecombination at a specific DNA sequence in pneumococcal transformation.

Authors:  J C Lefèvre; A M Gasc; A C Burger; P Mostachfi; A M Sicard
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

10.  Isolation of deoxyribonucleic acid methylase mutants of Escherichia coli K-12.

Authors:  M G Marinus; N R Morris
Journal:  J Bacteriol       Date:  1973-06       Impact factor: 3.490

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  31 in total

Review 1.  The structural basis of damaged DNA recognition and endonucleolytic cleavage for very short patch repair endonuclease.

Authors:  S E Tsutakawa; K Morikawa
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

2.  Nucleotide sequence of the Escherichia coli micA gene required for A/G-specific mismatch repair: identity of micA and mutY.

Authors:  J J Tsai-Wu; J P Radicella; A L Lu
Journal:  J Bacteriol       Date:  1991-03       Impact factor: 3.490

3.  Mismatch-specific thymine DNA glycosylase and DNA polymerase beta mediate the correction of G.T mispairs in nuclear extracts from human cells.

Authors:  K Wiebauer; J Jiricny
Journal:  Proc Natl Acad Sci U S A       Date:  1990-08       Impact factor: 11.205

4.  DNA mismatch correction by Very Short Patch repair may have altered the abundance of oligonucleotides in the E. coli genome.

Authors:  A S Bhagwat; M McClelland
Journal:  Nucleic Acids Res       Date:  1992-04-11       Impact factor: 16.971

5.  Short-patch reverse transcription in Escherichia coli.

Authors:  D S Thaler; G Tombline; K Zahn
Journal:  Genetics       Date:  1995-07       Impact factor: 4.562

6.  Mismatch repair in Xenopus egg extracts: DNA strand breaks act as signals rather than excision points.

Authors:  I Varlet; B Canard; P Brooks; G Cerovic; M Radman
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-17       Impact factor: 11.205

7.  Very short patch mismatch repair activity associated with gene dcm is not conferred by a plasmid coding for EcoRII methylase.

Authors:  M Lieb; A S Bhagwat
Journal:  J Bacteriol       Date:  1988-10       Impact factor: 3.490

8.  A gene required for very short patch repair in Escherichia coli is adjacent to the DNA cytosine methylase gene.

Authors:  A Sohail; M Lieb; M Dar; A S Bhagwat
Journal:  J Bacteriol       Date:  1990-08       Impact factor: 3.490

9.  HpaII methyltransferase is mutagenic in Escherichia coli.

Authors:  B Bandaru; M Wyszynski; A S Bhagwat
Journal:  J Bacteriol       Date:  1995-05       Impact factor: 3.490

10.  Cytosine deaminations catalyzed by DNA cytosine methyltransferases are unlikely to be the major cause of mutational hot spots at sites of cytosine methylation in Escherichia coli.

Authors:  M Wyszynski; S Gabbara; A S Bhagwat
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-15       Impact factor: 11.205

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