Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2000-8-10
pubmed:databankReference
pubmed:abstractText
In wild-type Escherichia coli, recognition of the recombination hotspot, chi (5'-GCTGGTGG-3'), by the RecBCD enzyme is central to homologous recombination. However, in the recC* class of RecBCD mutants, stimulation of recombination by the canonical chi sequence is not detectable, but the levels of homologous recombination are nearly wild-type. In vivo studies demonstrate that a member of this class of mutants, the recC1004 allele, encodes an enzyme that responds to a novel variant of chi, termed chi* (5'-GCTGGTGCTCG-3'). Here, we establish that, in vitro, the chi* sequence is recognized more efficiently by the RecBC(1004)D enzyme than is the wild-type chi. This is manifest by both a greater modification of nuclease activity and a higher stimulation of RecA protein-mediated joint molecule formation at chi* than at chi. Sequencing of the recC1004 gene revealed that it contains a frameshift mutation, which results in a replacement of nine of the wild-type amino acid residues by eight in the mutant protein, and defines a locus that is important for the specificity of chi-recognition. In addition, we show that this novel, 11 nucleotide chi* sequence also regulates the wild-type RecBCD enzyme, supporting the notion that variants of the canonical chi constitute a class of sequences that regulate the recombination function of RecBCD enzyme.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0022-2836
pubmed:author
pubmed:copyrightInfo
Copyright 2000 Academic Press.
pubmed:issnType
Print
pubmed:day
14
pubmed:volume
300
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
469-79
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:10884344-Alleles, pubmed-meshheading:10884344-Amino Acid Sequence, pubmed-meshheading:10884344-Base Pairing, pubmed-meshheading:10884344-Base Sequence, pubmed-meshheading:10884344-DNA, Bacterial, pubmed-meshheading:10884344-DNA, Single-Stranded, pubmed-meshheading:10884344-Enzyme Activation, pubmed-meshheading:10884344-Escherichia coli, pubmed-meshheading:10884344-Escherichia coli Proteins, pubmed-meshheading:10884344-Exodeoxyribonuclease V, pubmed-meshheading:10884344-Exodeoxyribonucleases, pubmed-meshheading:10884344-Genetic Variation, pubmed-meshheading:10884344-Molecular Sequence Data, pubmed-meshheading:10884344-Mutation, pubmed-meshheading:10884344-Nucleotides, pubmed-meshheading:10884344-Plasmids, pubmed-meshheading:10884344-Rec A Recombinases, pubmed-meshheading:10884344-Recombination, Genetic, pubmed-meshheading:10884344-Regulatory Sequences, Nucleic Acid, pubmed-meshheading:10884344-Substrate Specificity
pubmed:year
2000
pubmed:articleTitle
A novel, 11 nucleotide variant of chi, chi*: one of a class of sequences defining the Escherichia coli recombination hotspot chi.
pubmed:affiliation
Sections of Microbiology and of Molecular and Cellular Biology, University of California at Davis, CA 95616, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't