Literature DB >> 2645195

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

A M Gasc1, A M Sicard, J P Claverys.   

Abstract

The use as genetic markers, during transformation of Streptococcus pneumoniae, of 19 sequences differing from wild type, located throughout the amiA locus, enabled us to examine the fate of 24 single- and 11 multiple-mismatches during recombination. Tentative mismatch ranking as a function of decreasing repair efficiency by the Hex mismatch repair system is G/T = A/C = G/G (maximum repair: 90-95%) greater than C/T (mostly 75 to 90% repair) greater than A/A (from 50 to 90% repair) greater than T/T (50-65% repair) greater than A/G (from 0 to 20% repair) greater than C/C. No indication of correction of the latter has been obtained. Over the limited number of samples examined, we observed no influence of the base composition of the surrounding sequence on correction efficiency for both transition mismatches and for G/G and C/C. Variations in the surrounding sequence affect repair of A/G and C/T, and, even more strongly, of A/A and T/T. No simple correlation to the G:C content of the surrounding sequence is apparent from our results, in contrast to the conclusion drawn for the Mut mismatch repair system of Escherichia coli. Examination of the fate of multiple mismatches suggests that C/C may sometimes impede recognition of otherwise corrected mismatches.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2645195      PMCID: PMC1203602     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  24 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.  Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs.

Authors:  S S Su; P Modrich
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

3.  Frame-shift mutants induced by quinacrine are recognized by the mismatch repair system in Streptococcus pneumoniae.

Authors:  A M Gasc; A M Sicard
Journal:  Mol Gen Genet       Date:  1986-05

Review 4.  Mismatch repair in Escherichia coli.

Authors:  M Radman; R Wagner
Journal:  Annu Rev Genet       Date:  1986       Impact factor: 16.830

5.  Physical and genetic hybrids formed in bacterial transformation.

Authors:  T Gurney; M S Fox
Journal:  J Mol Biol       Date:  1968-02-28       Impact factor: 5.469

Review 6.  DNA mismatch correction.

Authors:  P Modrich
Journal:  Annu Rev Biochem       Date:  1987       Impact factor: 23.643

7.  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

8.  Structural studies of DNA fragments: the G.T wobble base pair in A, B and Z DNA; the G.A base pair in B-DNA.

Authors:  O Kennard
Journal:  J Biomol Struct Dyn       Date:  1985-10

9.  Repair of defined single base-pair mismatches in Escherichia coli.

Authors:  C Dohet; R Wagner; M Radman
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

10.  Structure of an adenine-cytosine base pair in DNA and its implications for mismatch repair.

Authors:  W N Hunter; T Brown; N N Anand; O Kennard
Journal:  Nature       Date:  1986 Apr 10-16       Impact factor: 49.962

View more
  18 in total

1.  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

2.  Characterization of the mycobacterial NER system reveals novel functions of the uvrD1 helicase.

Authors:  Carolin Güthlein; Roger M Wanner; Peter Sander; Elaine O Davis; Martin Bosshard; Josef Jiricny; Erik C Böttger; Burkhard Springer
Journal:  J Bacteriol       Date:  2008-11-14       Impact factor: 3.490

3.  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

4.  Extrahelical cytosine bases in DNA duplexes containing d[GCC](n).d[GCC](n) repeats: detection by a mechlorethamine crosslinking reaction.

Authors:  P Rojsitthisak; R M Romero; I S Haworth
Journal:  Nucleic Acids Res       Date:  2001-11-15       Impact factor: 16.971

5.  Barriers to genetic exchange between bacterial species: Streptococcus pneumoniae transformation.

Authors:  J Majewski; P Zawadzki; P Pickerill; F M Cohan; C G Dowson
Journal:  J Bacteriol       Date:  2000-02       Impact factor: 3.490

Review 6.  Bacterial gene transfer by natural genetic transformation in the environment.

Authors:  M G Lorenz; W Wackernagel
Journal:  Microbiol Rev       Date:  1994-09

7.  DNA sequence analysis of artificially evolved ebg enzyme and ebg repressor genes.

Authors:  B G Hall; P W Betts; J C Wootton
Journal:  Genetics       Date:  1989-12       Impact factor: 4.562

8.  Short-sequence tandem and nontandem DNA repeats and endogenous hydrogen peroxide production contribute to genetic instability of Streptococcus pneumoniae.

Authors:  Christopher D Pericone; Deborah Bae; Mikhail Shchepetov; Tera McCool; Jeffrey N Weiser
Journal:  J Bacteriol       Date:  2002-08       Impact factor: 3.490

9.  Mismatch repair genes of Streptococcus pneumoniae: HexA confers a mutator phenotype in Escherichia coli by negative complementation.

Authors:  M Prudhomme; V Méjean; B Martin; J P Claverys
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

10.  Gene localization, size, and physical map of the chromosome of Streptococcus pneumoniae.

Authors:  A M Gasc; L Kauc; P Barraillé; M Sicard; S Goodgal
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.