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On the Mechanism of Gene Silencing in Saccharomyces cerevisiae

Multiple mechanisms have been proposed for gene silencing in Saccharomyces cerevisiae, ranging from steric occlusion of DNA binding proteins from their recognition sequences in silenced chromatin to a specific block in the formation of the preinitiation complex to a block in transcriptional elongati...

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Autores principales: Steakley, David Lee, Rine, Jasper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528331/
https://www.ncbi.nlm.nih.gov/pubmed/26082137
http://dx.doi.org/10.1534/g3.115.018515
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author Steakley, David Lee
Rine, Jasper
author_facet Steakley, David Lee
Rine, Jasper
author_sort Steakley, David Lee
collection PubMed
description Multiple mechanisms have been proposed for gene silencing in Saccharomyces cerevisiae, ranging from steric occlusion of DNA binding proteins from their recognition sequences in silenced chromatin to a specific block in the formation of the preinitiation complex to a block in transcriptional elongation. This study provided strong support for the steric occlusion mechanism by the discovery that RNA polymerase of bacteriophage T7 could be substantially blocked from transcribing from its cognate promoter when embedded in silenced chromatin. Moreover, unlike previous suggestions, we found no evidence for stalled RNA polymerase II within silenced chromatin. The effectiveness of the Sir protein–based silencing mechanism to block transcription activated by Gal4 at promoters in the domain of silenced chromatin was marginal, yet it improved when tested against mutant forms of the Gal4 protein, highlighting a role for specific activators in their sensitivity to gene silencing.
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spelling pubmed-45283312015-08-10 On the Mechanism of Gene Silencing in Saccharomyces cerevisiae Steakley, David Lee Rine, Jasper G3 (Bethesda) Investigations Multiple mechanisms have been proposed for gene silencing in Saccharomyces cerevisiae, ranging from steric occlusion of DNA binding proteins from their recognition sequences in silenced chromatin to a specific block in the formation of the preinitiation complex to a block in transcriptional elongation. This study provided strong support for the steric occlusion mechanism by the discovery that RNA polymerase of bacteriophage T7 could be substantially blocked from transcribing from its cognate promoter when embedded in silenced chromatin. Moreover, unlike previous suggestions, we found no evidence for stalled RNA polymerase II within silenced chromatin. The effectiveness of the Sir protein–based silencing mechanism to block transcription activated by Gal4 at promoters in the domain of silenced chromatin was marginal, yet it improved when tested against mutant forms of the Gal4 protein, highlighting a role for specific activators in their sensitivity to gene silencing. Genetics Society of America 2015-06-16 /pmc/articles/PMC4528331/ /pubmed/26082137 http://dx.doi.org/10.1534/g3.115.018515 Text en Copyright © 2015 Steakley and Rine http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Steakley, David Lee
Rine, Jasper
On the Mechanism of Gene Silencing in Saccharomyces cerevisiae
title On the Mechanism of Gene Silencing in Saccharomyces cerevisiae
title_full On the Mechanism of Gene Silencing in Saccharomyces cerevisiae
title_fullStr On the Mechanism of Gene Silencing in Saccharomyces cerevisiae
title_full_unstemmed On the Mechanism of Gene Silencing in Saccharomyces cerevisiae
title_short On the Mechanism of Gene Silencing in Saccharomyces cerevisiae
title_sort on the mechanism of gene silencing in saccharomyces cerevisiae
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528331/
https://www.ncbi.nlm.nih.gov/pubmed/26082137
http://dx.doi.org/10.1534/g3.115.018515
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