Literature DB >> 7823316

Substrate preferences of Vsr DNA mismatch endonuclease and their consequences for the evolution of the Escherichia coli K-12 genome.

W Gläsner1, R Merkl, V Schellenberger, H J Fritz.   

Abstract

The substrate spectrum of Vsr DNA mismatch endonuclease of Escherichia coli K-12 was investigated using fluorescence-labelled oligonucleotide substrates and a DNA sequencer for detection and quantification of substrates and reaction products. Fourteen substrates were found to be processed by the enzyme, which differ in one or two positions from the canonical pentanucleotide sequence CTA/TGG (T mismatched to G). Relative second-order rate constants of these substrates were determined in groups of four by multiple substrate kinetics and compared to the underresentation of the corresponding pentanucleotides in the E. coli K-12 genome. The high quality of correlation further establishes active mutagenesis by VSP repair as a significant driving force of the evolution of the E. coli K-12 genome and provides clues to its possible selective value.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7823316     DOI: 10.1016/s0022-2836(95)80033-6

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


  24 in total

1.  A phylogenomic study of DNA repair genes, proteins, and processes.

Authors:  J A Eisen; P C Hanawalt
Journal:  Mutat Res       Date:  1999-12-07       Impact factor: 2.433

2.  Recognition of GT mismatches by Vsr mismatch endonuclease.

Authors:  K R Fox; S L Allinson; H Sahagun-Krause; T Brown
Journal:  Nucleic Acids Res       Date:  2000-07-01       Impact factor: 16.971

3.  Two amino acid replacements change the substrate preference of DNA mismatch glycosylase Mig.MthI from T/G to A/G.

Authors:  Yvonne N Fondufe-Mittendorf; Christine Härer; Wilfried Kramer; Hans-Joachim Fritz
Journal:  Nucleic Acids Res       Date:  2002-01-15       Impact factor: 16.971

Review 4.  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

5.  Very-short-patch repair in Escherichia coli requires the dam adenine methylase.

Authors:  D C Bell; C G Cupples
Journal:  J Bacteriol       Date:  2001-06       Impact factor: 3.490

6.  A novel type of uracil-DNA glycosylase mediating repair of hydrolytic DNA damage in the extremely thermophilic eubacterium Thermus thermophilus.

Authors:  Vytaute Starkuviene; Hans-Joachim Fritz
Journal:  Nucleic Acids Res       Date:  2002-05-15       Impact factor: 16.971

7.  Crystal structure of the Escherichia coli dcm very-short-patch DNA repair endonuclease bound to its reaction product-site in a DNA superhelix.

Authors:  Karen A Bunting; S Mark Roe; Anthony Headley; Tom Brown; Renos Savva; Laurence H Pearl
Journal:  Nucleic Acids Res       Date:  2003-03-15       Impact factor: 16.971

8.  A DNA methyltransferase can protect the genome from postdisturbance attack by a restriction-modification gene complex.

Authors:  Noriko Takahashi; Yasuhiro Naito; Naofumi Handa; Ichizo Kobayashi
Journal:  J Bacteriol       Date:  2002-11       Impact factor: 3.490

9.  The Escherichia coli MutL protein stimulates binding of Vsr and MutS to heteroduplex DNA.

Authors:  K Drotschmann; A Aronshtam; H J Fritz; M G Marinus
Journal:  Nucleic Acids Res       Date:  1998-02-15       Impact factor: 16.971

10.  Mismatch repair proteins collaborate with methyltransferases in the repair of O(6)-methylguanine.

Authors:  Peter T Rye; James C Delaney; Chawita Netirojjanakul; Dana X Sun; Jenny Z Liu; John M Essigmann
Journal:  DNA Repair (Amst)       Date:  2007-10-24
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.