Histone H2B repression causes cell-cycle-specific arrest in yeast: Effects on chromosomal segregation, replication, and transcription
Identifieur interne : 004C95 ( Main/Exploration ); précédent : 004C94; suivant : 004C96Histone H2B repression causes cell-cycle-specific arrest in yeast: Effects on chromosomal segregation, replication, and transcription
Auteurs : Min Han [États-Unis] ; Miles Chang [États-Unis] ; Ung-Jin Kim [États-Unis] ; Michael Grunstein [États-Unis]Source :
- Cell [ 0092-8674 ] ; 1987.
English descriptors
- Teeft :
- Acad, Biol, Cell cycle, Cell division, Cell number, Cellular processes, Cerevisiae, Channel numbers, Chromatin, Chromosomal, Chromosomal segregation, Chromosome, Chromosome structure, Cold spring harbor, Dapi, Experimental procedures, Full round, Galactose, Gene induction, Glucose, Glucose arrest, Glucose medium, Glucose repression, Grunstein, Hartwell, Hereford, High levels, Histone, Histone mrnas, Histone synthesis, Htbp gene, Hydroxyurea, Lethality, Mhylo2 cells, Mhylop, Mhylop cells, Micrococcal nuclease, Mitosis, Monoclonal antibody, Mrna, Mrna synthesis, Mutant, Mutation, Natl, Northern blot, Nuclear segregation, Nuclease, Nucleosome, Nucleosomes, Phenotype, Plasmid, Proc, Promoter, Replication, Room temperature, Saccharomyces, Saccharomyces cerevisiae, Simian virus, Superhelical, Superhelical density, Terminal phenotype, Time point, Time points, Transcription, Various media, Various times, Wallis, Yeast, Yeast cell cycle, Yeast strain, Yepd.
Abstract
Abstract: To determine which cellular processes are dependent on histones, we blocked histone H2B mRNA synthesis in asynchronously growing yeast after fusing the H2B gene to a repressible GAL10 promoter. Chromosomal segregation, replication, and transcription were then examined. We found that the cells arrested in mitosis, with a cell division cycle (cdc) phenotype. Chromatin structure and nuclear segregation were disrupted. A full round of DNA replication took place after the repression of histone H2B mRNA synthesis. Active transcription and the induction of new transcripts also continued in the arrested cells.
Url:
DOI: 10.1016/0092-8674(87)90237-6
Affiliations:
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Le document en format XML
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<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acad</term>
<term>Biol</term>
<term>Cell cycle</term>
<term>Cell division</term>
<term>Cell number</term>
<term>Cellular processes</term>
<term>Cerevisiae</term>
<term>Channel numbers</term>
<term>Chromatin</term>
<term>Chromosomal</term>
<term>Chromosomal segregation</term>
<term>Chromosome</term>
<term>Chromosome structure</term>
<term>Cold spring harbor</term>
<term>Dapi</term>
<term>Experimental procedures</term>
<term>Full round</term>
<term>Galactose</term>
<term>Gene induction</term>
<term>Glucose</term>
<term>Glucose arrest</term>
<term>Glucose medium</term>
<term>Glucose repression</term>
<term>Grunstein</term>
<term>Hartwell</term>
<term>Hereford</term>
<term>High levels</term>
<term>Histone</term>
<term>Histone mrnas</term>
<term>Histone synthesis</term>
<term>Htbp gene</term>
<term>Hydroxyurea</term>
<term>Lethality</term>
<term>Mhylo2 cells</term>
<term>Mhylop</term>
<term>Mhylop cells</term>
<term>Micrococcal nuclease</term>
<term>Mitosis</term>
<term>Monoclonal antibody</term>
<term>Mrna</term>
<term>Mrna synthesis</term>
<term>Mutant</term>
<term>Mutation</term>
<term>Natl</term>
<term>Northern blot</term>
<term>Nuclear segregation</term>
<term>Nuclease</term>
<term>Nucleosome</term>
<term>Nucleosomes</term>
<term>Phenotype</term>
<term>Plasmid</term>
<term>Proc</term>
<term>Promoter</term>
<term>Replication</term>
<term>Room temperature</term>
<term>Saccharomyces</term>
<term>Saccharomyces cerevisiae</term>
<term>Simian virus</term>
<term>Superhelical</term>
<term>Superhelical density</term>
<term>Terminal phenotype</term>
<term>Time point</term>
<term>Time points</term>
<term>Transcription</term>
<term>Various media</term>
<term>Various times</term>
<term>Wallis</term>
<term>Yeast</term>
<term>Yeast cell cycle</term>
<term>Yeast strain</term>
<term>Yepd</term>
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<front><div type="abstract" xml:lang="en">Abstract: To determine which cellular processes are dependent on histones, we blocked histone H2B mRNA synthesis in asynchronously growing yeast after fusing the H2B gene to a repressible GAL10 promoter. Chromosomal segregation, replication, and transcription were then examined. We found that the cells arrested in mitosis, with a cell division cycle (cdc) phenotype. Chromatin structure and nuclear segregation were disrupted. A full round of DNA replication took place after the repression of histone H2B mRNA synthesis. Active transcription and the induction of new transcripts also continued in the arrested cells.</div>
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<tree><country name="États-Unis"><region name="Californie"><name sortKey="Han, Min" sort="Han, Min" uniqKey="Han M" first="Min" last="Han">Min Han</name>
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<name sortKey="Chang, Miles" sort="Chang, Miles" uniqKey="Chang M" first="Miles" last="Chang">Miles Chang</name>
<name sortKey="Chang, Miles" sort="Chang, Miles" uniqKey="Chang M" first="Miles" last="Chang">Miles Chang</name>
<name sortKey="Grunstein, Michael" sort="Grunstein, Michael" uniqKey="Grunstein M" first="Michael" last="Grunstein">Michael Grunstein</name>
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<name sortKey="Han, Min" sort="Han, Min" uniqKey="Han M" first="Min" last="Han">Min Han</name>
<name sortKey="Kim, Ung Jin" sort="Kim, Ung Jin" uniqKey="Kim U" first="Ung-Jin" last="Kim">Ung-Jin Kim</name>
<name sortKey="Kim, Ung Jin" sort="Kim, Ung Jin" uniqKey="Kim U" first="Ung-Jin" last="Kim">Ung-Jin Kim</name>
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