Literature DB >> 6929947

Excision and repair of mismatched base pairs in transformation of Streptococcus pneumoniae.

J P Claverys, M Roger, A M Sicard.   

Abstract

The use of heteroduplex DNA molecules as donors in pneumococcal transformation makes it possible to follow the fate of each DNA strand. The integration efficiency of each strand depends strongly upon the single base changes it carries. The function (hex) which reduces drastically the transformation yield of markers referred to as low efficiency (LE) tends to remove either donor strand without respect ot which one is introduced. In the case of high efficiency (HE) markers the reduction in the transformation yield involves the elimination of only one donor strand. For a given locus it can be either one depending upon the mutation. The reduction in transformation yield can be less drastic for HE markers than for both strands of the LE markers. These data are discussed in terms of differences in the affinity for mismatched base pairs. We have studied the transfer of information from each donor DNA strand to the recipient genome, on the basis of differences in the rates of phenotypic expression of a given marker introduced on opposite strands. Results show that, as in the case of LE markers, the information from HE markers, when introduced on the strand recognized by the hex function, is transmitted to both strands of the recipient molecule. Correction of the recipient strand to homozygosis probably accounts for this information transfer. These results, together with earlier investigations, strongly suggest that the hex function is an excision-repair system acting on donor-recipient base pair mismatches.

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Year:  1980        PMID: 6929947     DOI: 10.1007/bf00267229

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


  37 in total

1.  A NEW SYNTHETIC MEDIUM FOR DIPLOCOCCUS PNEUMONIAE, AND ITS USE FOR THE STUDY OF RECIPROCAL TRANSFORMATIONS AT THE AMIA LOCUS.

Authors:  A M SICARD
Journal:  Genetics       Date:  1964-07       Impact factor: 4.562

2.  Genetic recombination in DNA-induced transformation of Pneumococcus. II. Mapping the amiA region.

Authors:  A M Sicard; H Ephrussi-Taylor
Journal:  Genetics       Date:  1965-12       Impact factor: 4.562

3.  [Action of ultraviolet radiation on the integration of genetic markers during transformation in Diplococcus pneumoniae].

Authors:  J M Louarn
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1966-01-10

4.  Differences in rate of phenotypic expression in separated strands of pneumococcal transforming DNA and evidence for change of reading direction.

Authors:  M Gabor; R D Hotchkiss
Journal:  Genetics       Date:  1969       Impact factor: 4.562

5.  Genetic recombination in DNA-induced transformation of Pneumococcus. IV. The pattern of transmission and phenotypic expression of high and low-efficiency donor sites in the amiA locus.

Authors:  H Ephrussi-Taylor
Journal:  Genetics       Date:  1966-07       Impact factor: 4.562

6.  Integration efficiencies of spontaneous mutant alleles of amiA locus in pneumococcal transformation.

Authors:  G Tiraby; M A Sicard
Journal:  J Bacteriol       Date:  1973-12       Impact factor: 3.490

7.  Marker discrimination in transformation and mutation of pneumococcus.

Authors:  J G Tiraby; M S Fox
Journal:  Proc Natl Acad Sci U S A       Date:  1973-12       Impact factor: 11.205

8.  Marker discrimination and mutagen-induced alterations in pneumococcal transformation.

Authors:  J G Tiraby; M S Fox
Journal:  Genetics       Date:  1974-07       Impact factor: 4.562

9.  Destruction of low efficiency markers is a slow process occurring at a heteroduplex stage of transformation.

Authors:  N B Shoemaker; W R Guild
Journal:  Mol Gen Genet       Date:  1974

10.  Mechanism of inhibition of Bacillus subtilis DNA polymerase 3 by the arylhydrazinopyrimidine antimicrobial agents.

Authors:  R L Low; S A Rashbaum; N R Cozzarelli
Journal:  Proc Natl Acad Sci U S A       Date:  1974-08       Impact factor: 11.205

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  36 in total

1.  Polarity of recombination in transformation of Streptococcus pneumoniae.

Authors:  F Pasta; M A Sicard
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

2.  The high level streptomycin resistance gene from Streptococcus pneumoniae is a homologue of the ribosomal protein S12 gene from Escherichia coli.

Authors:  C Salles; L Créancier; J P Claverys; V Méjean
Journal:  Nucleic Acids Res       Date:  1992-11-25       Impact factor: 16.971

3.  Nucleotide sequence of the Streptococcus pneumoniae ung gene encoding uracil-DNA glycosylase.

Authors:  V Méjean; I Rives; J P Claverys
Journal:  Nucleic Acids Res       Date:  1990-11-25       Impact factor: 16.971

4.  Repair of single- and multiple-substitution mismatches during recombination in Streptococcus pneumoniae.

Authors:  A M Gasc; A M Sicard; J P Claverys
Journal:  Genetics       Date:  1989-01       Impact factor: 4.562

5.  Uracil-DNA glycosylase affects mismatch repair efficiency in transformation and bisulfite-induced mutagenesis in Streptococcus pneumoniae.

Authors:  V Méjean; J C Devedjian; I Rives; G Alloing; J P Claverys
Journal:  Nucleic Acids Res       Date:  1991-10-25       Impact factor: 16.971

6.  Role of uracil-DNA glycosylase in mutation avoidance by Streptococcus pneumoniae.

Authors:  J D Chen; S A Lacks
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

7.  Conversion of deletions during recombination in pneumococcal transformation.

Authors:  J C Lefèvre; P Mostachfi; A M Gasc; E Guillot; F Pasta; M Sicard
Journal:  Genetics       Date:  1989-11       Impact factor: 4.562

8.  The hexB mismatch repair gene of Streptococcus pneumoniae: characterisation, cloning and identification of the product.

Authors:  H Prats; B Martin; J P Claverys
Journal:  Mol Gen Genet       Date:  1985

9.  Meiotic gene conversion mutants in Saccharomyces cerevisiae. I. Isolation and characterization of pms1-1 and pms1-2.

Authors:  M S Williamson; J C Game; S Fogel
Journal:  Genetics       Date:  1985-08       Impact factor: 4.562

10.  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

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