Identification of a Shigella flexneri criR gene increasing ipa genes expression: a novel member of response regulators of the two-component signal transduction family.
{"title":"Identification of a Shigella flexneri criR gene increasing ipa genes expression: a novel member of response regulators of the two-component signal transduction family.","authors":"M S Qi, H Yoshikura, H Watanabe","doi":"10.7883/yoken1952.49.219","DOIUrl":null,"url":null,"abstract":"<p><p>A genetic locus named cri, which enhanced the expression of ipa genes, was cloned into Escherichia coli K-12 from Shigella flexneri 1b chromosomal DNA. Subcloning and Tn5-Tc1 transposon experiments showed that cri locus was located on a 2.6-kb HindIII fragment. Nucleotide sequence analysis of the region revealed at least three open reading frames (ORF), one of which, named criR, encoded a protein of 226 amino-acid residues and transcriptionally increased the ipaB expression. The deduced regulatory protein CriR shared a significant homology with bacterial transcriptional activators of the two-component signal transduction family. A homologue of the criR gene was present in genomic DNA of Shigella spp. and E. coli strains, and mapped at the 14.6-min region of E. coli K-12 chromosomal DNA. These results indicate that criR is a new member of response regulators.</p>","PeriodicalId":14531,"journal":{"name":"Japanese journal of medical science & biology","volume":"49 5-6","pages":"219-39"},"PeriodicalIF":0.0000,"publicationDate":"1996-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese journal of medical science & biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7883/yoken1952.49.219","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
A genetic locus named cri, which enhanced the expression of ipa genes, was cloned into Escherichia coli K-12 from Shigella flexneri 1b chromosomal DNA. Subcloning and Tn5-Tc1 transposon experiments showed that cri locus was located on a 2.6-kb HindIII fragment. Nucleotide sequence analysis of the region revealed at least three open reading frames (ORF), one of which, named criR, encoded a protein of 226 amino-acid residues and transcriptionally increased the ipaB expression. The deduced regulatory protein CriR shared a significant homology with bacterial transcriptional activators of the two-component signal transduction family. A homologue of the criR gene was present in genomic DNA of Shigella spp. and E. coli strains, and mapped at the 14.6-min region of E. coli K-12 chromosomal DNA. These results indicate that criR is a new member of response regulators.
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