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Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III–transcribed genes in budding yeast

The association of RNA polymerase III (Pol III)–transcribed genes with nucleoli seems to be an evolutionarily conserved property of the spatial organization of eukaryotic genomes. However, recent studies of global chromosome architecture in budding yeast have challenged this view. We used live-cell...

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Autores principales: Belagal, Praveen, Normand, Christophe, Shukla, Ashutosh, Wang, Renjie, Léger-Silvestre, Isabelle, Dez, Christophe, Bhargava, Purnima, Gadal, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063623/
https://www.ncbi.nlm.nih.gov/pubmed/27559135
http://dx.doi.org/10.1091/mbc.E16-03-0145
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author Belagal, Praveen
Normand, Christophe
Shukla, Ashutosh
Wang, Renjie
Léger-Silvestre, Isabelle
Dez, Christophe
Bhargava, Purnima
Gadal, Olivier
author_facet Belagal, Praveen
Normand, Christophe
Shukla, Ashutosh
Wang, Renjie
Léger-Silvestre, Isabelle
Dez, Christophe
Bhargava, Purnima
Gadal, Olivier
author_sort Belagal, Praveen
collection PubMed
description The association of RNA polymerase III (Pol III)–transcribed genes with nucleoli seems to be an evolutionarily conserved property of the spatial organization of eukaryotic genomes. However, recent studies of global chromosome architecture in budding yeast have challenged this view. We used live-cell imaging to determine the intranuclear positions of 13 Pol III–transcribed genes. The frequency of association with nucleolus and nuclear periphery depends on linear genomic distance from the tethering elements—centromeres or telomeres. Releasing the hold of the tethering elements by inactivating centromere attachment to the spindle pole body or changing the position of ribosomal DNA arrays resulted in the association of Pol III–transcribed genes with nucleoli. Conversely, ectopic insertion of a Pol III–transcribed gene in the vicinity of a centromere prevented its association with nucleolus. Pol III–dependent transcription was independent of the intranuclear position of the gene, but the nucleolar recruitment of Pol III–transcribed genes required active transcription. We conclude that the association of Pol III–transcribed genes with the nucleolus, when permitted by global chromosome architecture, provides nucleolar and/or nuclear peripheral anchoring points contributing locally to intranuclear chromosome organization.
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spelling pubmed-50636232016-12-30 Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III–transcribed genes in budding yeast Belagal, Praveen Normand, Christophe Shukla, Ashutosh Wang, Renjie Léger-Silvestre, Isabelle Dez, Christophe Bhargava, Purnima Gadal, Olivier Mol Biol Cell Articles The association of RNA polymerase III (Pol III)–transcribed genes with nucleoli seems to be an evolutionarily conserved property of the spatial organization of eukaryotic genomes. However, recent studies of global chromosome architecture in budding yeast have challenged this view. We used live-cell imaging to determine the intranuclear positions of 13 Pol III–transcribed genes. The frequency of association with nucleolus and nuclear periphery depends on linear genomic distance from the tethering elements—centromeres or telomeres. Releasing the hold of the tethering elements by inactivating centromere attachment to the spindle pole body or changing the position of ribosomal DNA arrays resulted in the association of Pol III–transcribed genes with nucleoli. Conversely, ectopic insertion of a Pol III–transcribed gene in the vicinity of a centromere prevented its association with nucleolus. Pol III–dependent transcription was independent of the intranuclear position of the gene, but the nucleolar recruitment of Pol III–transcribed genes required active transcription. We conclude that the association of Pol III–transcribed genes with the nucleolus, when permitted by global chromosome architecture, provides nucleolar and/or nuclear peripheral anchoring points contributing locally to intranuclear chromosome organization. The American Society for Cell Biology 2016-10-15 /pmc/articles/PMC5063623/ /pubmed/27559135 http://dx.doi.org/10.1091/mbc.E16-03-0145 Text en © 2016 Belagal et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Belagal, Praveen
Normand, Christophe
Shukla, Ashutosh
Wang, Renjie
Léger-Silvestre, Isabelle
Dez, Christophe
Bhargava, Purnima
Gadal, Olivier
Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III–transcribed genes in budding yeast
title Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III–transcribed genes in budding yeast
title_full Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III–transcribed genes in budding yeast
title_fullStr Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III–transcribed genes in budding yeast
title_full_unstemmed Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III–transcribed genes in budding yeast
title_short Decoding the principles underlying the frequency of association with nucleoli for RNA polymerase III–transcribed genes in budding yeast
title_sort decoding the principles underlying the frequency of association with nucleoli for rna polymerase iii–transcribed genes in budding yeast
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063623/
https://www.ncbi.nlm.nih.gov/pubmed/27559135
http://dx.doi.org/10.1091/mbc.E16-03-0145
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