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Increased transcription in hydroxyurea-treated root meristem cells of Vicia faba

Hydroxyurea (HU), an inhibitor of ribonucleotide reductase, prevents cells from progressing through S phase by depletion of deoxyribonucleoside triphosphates. Concurrently, disruption of DNA replication leads to double-strand DNA breaks. In root meristems of Vicia faba, HU triggers cell cycle arrest...

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Detalles Bibliográficos
Autores principales: Winnicki, Konrad, Polit, Justyna Teresa, Maszewski, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557396/
https://www.ncbi.nlm.nih.gov/pubmed/22526201
http://dx.doi.org/10.1007/s00709-012-0402-x
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author Winnicki, Konrad
Polit, Justyna Teresa
Maszewski, Janusz
author_facet Winnicki, Konrad
Polit, Justyna Teresa
Maszewski, Janusz
author_sort Winnicki, Konrad
collection PubMed
description Hydroxyurea (HU), an inhibitor of ribonucleotide reductase, prevents cells from progressing through S phase by depletion of deoxyribonucleoside triphosphates. Concurrently, disruption of DNA replication leads to double-strand DNA breaks. In root meristems of Vicia faba, HU triggers cell cycle arrest (preferentially in G1/S phase) and changes an overall metabolism by global activation of transcription both in the nucleoplasmic and nucleolar regions. High level of transcription is accompanied by an increase in the content of RNA polymerase II large subunit (POLR2A). Changes in transcription activation and POLR2A content correlate with posttranslational modifications of histones that play a role in opening up chromatin for transcription. Increase in the level of H4 Lys5 acetylation indicates that global activation of transcription following HU treatment depends on histone modifications.
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spelling pubmed-35573962013-01-29 Increased transcription in hydroxyurea-treated root meristem cells of Vicia faba Winnicki, Konrad Polit, Justyna Teresa Maszewski, Janusz Protoplasma Original Article Hydroxyurea (HU), an inhibitor of ribonucleotide reductase, prevents cells from progressing through S phase by depletion of deoxyribonucleoside triphosphates. Concurrently, disruption of DNA replication leads to double-strand DNA breaks. In root meristems of Vicia faba, HU triggers cell cycle arrest (preferentially in G1/S phase) and changes an overall metabolism by global activation of transcription both in the nucleoplasmic and nucleolar regions. High level of transcription is accompanied by an increase in the content of RNA polymerase II large subunit (POLR2A). Changes in transcription activation and POLR2A content correlate with posttranslational modifications of histones that play a role in opening up chromatin for transcription. Increase in the level of H4 Lys5 acetylation indicates that global activation of transcription following HU treatment depends on histone modifications. Springer Vienna 2012-04-15 2013 /pmc/articles/PMC3557396/ /pubmed/22526201 http://dx.doi.org/10.1007/s00709-012-0402-x Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Winnicki, Konrad
Polit, Justyna Teresa
Maszewski, Janusz
Increased transcription in hydroxyurea-treated root meristem cells of Vicia faba
title Increased transcription in hydroxyurea-treated root meristem cells of Vicia faba
title_full Increased transcription in hydroxyurea-treated root meristem cells of Vicia faba
title_fullStr Increased transcription in hydroxyurea-treated root meristem cells of Vicia faba
title_full_unstemmed Increased transcription in hydroxyurea-treated root meristem cells of Vicia faba
title_short Increased transcription in hydroxyurea-treated root meristem cells of Vicia faba
title_sort increased transcription in hydroxyurea-treated root meristem cells of vicia faba
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557396/
https://www.ncbi.nlm.nih.gov/pubmed/22526201
http://dx.doi.org/10.1007/s00709-012-0402-x
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