Identification of sequences in a yeast histone promoter involved in periodic transcription
Identifieur interne : 003E23 ( Main/Merge ); précédent : 003E22; suivant : 003E24Identification of sequences in a yeast histone promoter involved in periodic transcription
Auteurs : Mary Ann Osley [États-Unis] ; Jane Gould [États-Unis, Royaume-Uni] ; Sunyoung Kim [États-Unis, Royaume-Uni] ; Michael Kane [États-Unis] ; Lynna Hereford [États-Unis]Source :
- Cell [ 0092-8674 ] ; 1985.
Abstract
Sequences between a pair of divergently transcribed histone genes in Saccharomyces cerevisiae are able to confer periodic transcription during the cell cycle. This conclusion contrasts to our previous hypothesis that an ars (autonomously replicating sequence) 3′ to this locus is a transcription timer for yeast histone genes. The promoter sequences required for periodic expression have been localized by deletion analysis, and isolated elements have been analyzed by insertion into a heterologous promoter. Two cell-cycle-specific promoter functions have been identified. One function activates transcription in a cell-cycle-dependent manner. The other periodically represses transcription. Negative regulation may be the predominant form of cell-cycle control, because removal of the repressing function results in constitutive expression of the histone genes.
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DOI: 10.1016/0092-8674(86)90285-0
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Boston</wicri:cityArea></affiliation><affiliation wicri:level="2"><country>Royaume-Uni</country><placeName><region type="country">Angleterre</region></placeName><wicri:cityArea>★ Present address: Department of Biological Sciences, University of Warwick, Coventry, West Midlands</wicri:cityArea></affiliation></author><author><name sortKey="Kim, Sunyoung" sort="Kim, Sunyoung" uniqKey="Kim S" first="Sunyoung" last="Kim">Sunyoung Kim</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><placeName><region type="state">Massachusetts</region></placeName><wicri:cityArea>Dana-Farber Cancer Institute 44 Binney Street Boston</wicri:cityArea></affiliation><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><placeName><region type="state">Massachusetts</region></placeName><wicri:cityArea>Department of Microbiology and Molecular Genetics Harvard Medical School Boston</wicri:cityArea></affiliation><affiliation 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This conclusion contrasts to our previous hypothesis that an ars (autonomously replicating sequence) 3′ to this locus is a transcription timer for yeast histone genes. The promoter sequences required for periodic expression have been localized by deletion analysis, and isolated elements have been analyzed by insertion into a heterologous promoter. Two cell-cycle-specific promoter functions have been identified. One function activates transcription in a cell-cycle-dependent manner. The other periodically represses transcription. Negative regulation may be the predominant form of cell-cycle control, because removal of the repressing function results in constitutive expression of the histone genes.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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