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Transcription of alpha-tubulin and histone H4 genes begins at the same point in the Physarum cell cycle

In naturally synchronous plasmodia of Physarum polycephalum, both tubulin and histone gene transcription define periodic cell cycle- regulated events. Using a slot-blot hybridization assay and Northern blot analysis, we have demonstrated that a major peak of accumulation of both alpha-tubulin and hi...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1986
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114201/
https://www.ncbi.nlm.nih.gov/pubmed/3700471
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description In naturally synchronous plasmodia of Physarum polycephalum, both tubulin and histone gene transcription define periodic cell cycle- regulated events. Using a slot-blot hybridization assay and Northern blot analysis, we have demonstrated that a major peak of accumulation of both alpha-tubulin and histone H4 transcripts occurs in late G2 phase. Nuclear transcription assays indicate that both genes are transcriptionally activated at the same point in the cell cycle: mid G2 phase. While the rate of tubulin gene transcription drops sharply at the M/S-phase boundary, the rate of histone gene transcription remains high through most of S phase. We conclude that the cell cycle regulation of tubulin expression occurs primarily at the level of transcription, while histone regulation involves both transcriptional and posttranscriptional controls. It is possible that the periodic expression of both histone and tubulin genes is triggered by a common cell cycle regulatory mechanism.
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spelling pubmed-21142012008-05-01 Transcription of alpha-tubulin and histone H4 genes begins at the same point in the Physarum cell cycle J Cell Biol Articles In naturally synchronous plasmodia of Physarum polycephalum, both tubulin and histone gene transcription define periodic cell cycle- regulated events. Using a slot-blot hybridization assay and Northern blot analysis, we have demonstrated that a major peak of accumulation of both alpha-tubulin and histone H4 transcripts occurs in late G2 phase. Nuclear transcription assays indicate that both genes are transcriptionally activated at the same point in the cell cycle: mid G2 phase. While the rate of tubulin gene transcription drops sharply at the M/S-phase boundary, the rate of histone gene transcription remains high through most of S phase. We conclude that the cell cycle regulation of tubulin expression occurs primarily at the level of transcription, while histone regulation involves both transcriptional and posttranscriptional controls. It is possible that the periodic expression of both histone and tubulin genes is triggered by a common cell cycle regulatory mechanism. The Rockefeller University Press 1986-05-01 /pmc/articles/PMC2114201/ /pubmed/3700471 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Transcription of alpha-tubulin and histone H4 genes begins at the same point in the Physarum cell cycle
title Transcription of alpha-tubulin and histone H4 genes begins at the same point in the Physarum cell cycle
title_full Transcription of alpha-tubulin and histone H4 genes begins at the same point in the Physarum cell cycle
title_fullStr Transcription of alpha-tubulin and histone H4 genes begins at the same point in the Physarum cell cycle
title_full_unstemmed Transcription of alpha-tubulin and histone H4 genes begins at the same point in the Physarum cell cycle
title_short Transcription of alpha-tubulin and histone H4 genes begins at the same point in the Physarum cell cycle
title_sort transcription of alpha-tubulin and histone h4 genes begins at the same point in the physarum cell cycle
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114201/
https://www.ncbi.nlm.nih.gov/pubmed/3700471