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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 : 004C96

Histone 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 :

RBID : ISTEX:B35722EA7529EAC518C3D6FD4226FCF64234CCAC

English descriptors

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:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Cell number</term>
<term>Cellular processes</term>
<term>Cerevisiae</term>
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<term>Histone</term>
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<term>Histone synthesis</term>
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<term>Proc</term>
<term>Promoter</term>
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<term>Saccharomyces</term>
<term>Saccharomyces cerevisiae</term>
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<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>
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<term>Yeast</term>
<term>Yeast cell cycle</term>
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<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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