Restoration of bacterioopsin gene expression in a revertant of Halobacterium halobium

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Published inJournal of Bacteriology Vol. 164; no. 1; pp. 414 - 420
Main Authors PFEIFER, F. A, BOYER, H. W, BETLACH, M. C
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for Microbiology 01.10.1985
Subjects
Bacteriology
Bacteriorhodopsins - genetics
Biological and medical sciences
Carotenoids - genetics
DNA Transposable Elements
Fundamental and applied biological sciences. Psychology
Genes, Bacterial
Genetics
Halobacterium - genetics
Microbiology
Mutation
Nucleic Acid Hybridization
Transcription, Genetic
Molecular hybridization
RNA
Nucleotide sequence
Archaebacteria
Affinity chromatography
DNA
Restriction map
Insertion
Bacteria
Halobacteriaceae
Gene expression
Halobacterium halobium
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Abstract Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue JB About JB Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy JB RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0021-9193 Online ISSN: 1098-5530 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to JB .asm.org, visit: JB       
AbstractList Restoration of bacterioopsin (bop) gene expression in a revertant of Halobacterium halobium was investigated. The phenotype of the revertant is the result of a translocation of the 588-base-pair (bp) sequence "ISH25", adjacent to an ISH24 insertion found in the parental mutant IV-4. These insertions are located about 1,400 bp upstream of the bop gene within the coding region of the putative brp (bacterioopsin-related protein) gene. The level at which the brp gene affects bop gene expression is unknown. Analysis of bop and brp gene transcription in the wild type, mutant IV-4, and the revertant supports the hypothesis that transcription of the putative brp gene is necessary for bop gene expression in the revertant. Eight insertion mutants of the Bop revertant were analyzed to further elucidate restoration of bop gene expression in the revertant. Bop mutants of the revertant were recovered with a frequency of about 10(-4) and were found to contain insertion elements in addition to ISH24 and "ISH25". Six-eighths of these mutants have the insertion element ISH2, and two mutants have previously uncharacterized insertion elements (ISH27 [1,400 bp] and ISH28 [1,000 bp]). ISH27 and ISH28 are confined to the more A + T-rich fraction of the H. halobium genome, as are most copies of other halobacterial insertion elements. The insertion sites in the Bop mutants of the revertant mapped within the coding region of the bop gene (three mutants), immediately upstream of the bop gene presumably in the bop promoter region (two mutants), or within a region from 241 to 449 bp upstream of the bop gene (three mutants). This distribution of insertion sites suggests that the integrity of the 526-bp region between the bop and the brp genes is important for bop gene expression in the revertant.
Restoration of bacterioopsin (bop ) gene expression in a revertant of H. halobium was investigated. The phenotype of the revertant is the result of a translocation of the 588-base-pair (bp) sequence "ISH25", adjacent to an ISH24 insertion found in the parental mutant IV-4. These insertions are located about 1,400 bp upstream of the bop gene within the coding region of the putative brp (bacterioopsin-related protein) gene. The level at which the brp gene affects bop gene expression is unknown. Analysis of bop and brp gene transcription in the wild type, mutant IV-4, and the revertant supports the hypothesis that transcription of the putative brp gene is necessary for bop gene expression in the revertant. The insertaion sites in the Bop mutants of the revertant mapped within the coding region of the bop gene (three mutants), immediately upstream of the bop gene presumably in the bop promoter region (two mutants), or within a region from 241 to 449 bp upstream of the bop gene (three mutants). This distribution of insertion sites suggests that the integrity of the 526-bop region between the bop and the brp genes is important for bop gene expression in the revertant.
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Author H W Boyer
F A Pfeifer
M C Betlach
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Issue 1
Keywords Molecular hybridization
RNA
Nucleotide sequence
Archaebacteria
Affinity chromatography
DNA
Restriction map
Insertion
Bacteria
Halobacteriaceae
Gene expression
Halobacterium halobium
Language English
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Restoration of bacterioopsin (bop) gene expression in a revertant of Halobacterium halobium was investigated. The phenotype of the revertant is the result of a...
Restoration of bacterioopsin (bop ) gene expression in a revertant of H. halobium was investigated. The phenotype of the revertant is the result of a...
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StartPage 414
SubjectTerms Bacteriology
Bacteriorhodopsins - genetics
Biological and medical sciences
Carotenoids - genetics
DNA Transposable Elements
Fundamental and applied biological sciences. Psychology
Genes, Bacterial
Genetics
Halobacterium - genetics
Microbiology
Mutation
Nucleic Acid Hybridization
Transcription, Genetic
Title Restoration of bacterioopsin gene expression in a revertant of Halobacterium halobium
URI http://jb.asm.org/content/164/1/414.abstract
https://www.ncbi.nlm.nih.gov/pubmed/2995317
https://search.proquest.com/docview/14205787
https://search.proquest.com/docview/76386804
https://pubmed.ncbi.nlm.nih.gov/PMC214260
Volume 164
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