Literature DB >> 7596285

Boundaries of the nicking region for the F plasmid transfer origin, oriT.

Y Luo1, Q Gao, R C Deonier.   

Abstract

The extent of the F plasmid oriT nicking region was determined from the properties of successive substitution mutations in the region from base pair 121 to base pair 174 and from KMnO4 probing of DNA structural distortions induced in vivo by tra gene products. Nicking and transfer assays indicated that the left margin of oriT lies predominantly at the nick site, and that the nicking domain primarily lies within 17 bp to the right of the nick. Some mutants that were proficient for nicking showed reduced frequencies of termination, indicating that oriT nicking does not guarantee efficient termination. DNA in the vicinity of the nick (G137, T138, G140, and T141 on the nicked strand) showed elevated sensitivity to KMnO4 when tra gene products were present in the donor. Bases C145, C146, C147, C149, and G150 on the unnicked strand also became more sensitive to oxidation under tra+ conditions. The bases preferentially oxidized by KMnO4 lie within the nicking domain, as defined by the substitution mutants, and they include dinucleotides that can produce kinks in the DNA. Base pairs in the nicking region are calculated to be more thermodynamically stable than base pairs in the flanking regions.

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Year:  1995        PMID: 7596285     DOI: 10.1111/j.1365-2958.1995.tb02353.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  4 in total

1.  TraY and integration host factor oriT binding sites and F conjugal transfer: sequence variations, but not altered spacing, are tolerated.

Authors:  Sarah L Williams; Joel F Schildbach
Journal:  J Bacteriol       Date:  2007-03-09       Impact factor: 3.490

2.  Localization of the nic site of IncN conjugative plasmid pCU1 through formation of a hybrid oriT.

Authors:  E S Paterson; V N Iyer
Journal:  J Bacteriol       Date:  1997-09       Impact factor: 3.490

3.  Examination of an inverted repeat within the F factor origin of transfer: context dependence of F TraI relaxase DNA specificity.

Authors:  Sarah L Williams; Joel F Schildbach
Journal:  Nucleic Acids Res       Date:  2006-01-17       Impact factor: 16.971

4.  Engineering Infrequent DNA Nicking Endonuclease by Fusion of a BamHI Cleavage-Deficient Mutant and a DNA Nicking Domain.

Authors:  Shuang-Yong Xu
Journal:  Front Microbiol       Date:  2022-02-01       Impact factor: 5.640

  4 in total

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