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The YEATS domain of Taf14 in Saccharomyces cerevisiae has a negative impact on cell growth

The role of a highly conserved YEATS protein motif is explored in the context of the Taf14 protein of Saccharomyces cerevisiae. In S. cerevisiae, Taf14 is a protein physically associated with many critical multisubunit complexes including the general transcription factors TFIID and TFIIF, the chroma...

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Autores principales: Schulze, Julia M., Kane, Caroline M., Ruiz-Manzano, Ana
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839515/
https://www.ncbi.nlm.nih.gov/pubmed/20179968
http://dx.doi.org/10.1007/s00438-010-0523-x
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author Schulze, Julia M.
Kane, Caroline M.
Ruiz-Manzano, Ana
author_facet Schulze, Julia M.
Kane, Caroline M.
Ruiz-Manzano, Ana
author_sort Schulze, Julia M.
collection PubMed
description The role of a highly conserved YEATS protein motif is explored in the context of the Taf14 protein of Saccharomyces cerevisiae. In S. cerevisiae, Taf14 is a protein physically associated with many critical multisubunit complexes including the general transcription factors TFIID and TFIIF, the chromatin remodeling complexes SWI/SNF, Ino80 and RSC, Mediator and the histone modification enzyme NuA3. Taf14 is a member of the YEATS superfamily, conserved from bacteria to eukaryotes and thought to have a transcription stimulatory activity. However, besides its ubiquitous presence and its links with transcription, little is known about Taf14’s role in the nucleus. We use structure–function and mutational analysis to study the function of Taf14 and its well conserved N-terminal YEATS domain. We show here that the YEATS domain is not necessary for Taf14’s association with these transcription and chromatin remodeling complexes, and that its presence in these complexes is dependent only on its C-terminal domain. Our results also indicate that Taf14’s YEATS domain is not necessary for complementing the synthetic lethality between TAF14 and the general transcription factor TFIIS (encoded by DST1). Furthermore, we present evidence that the YEATS domain of Taf14 has a negative impact on cell growth: its absence enables cells to grow better than wild-type cells under stress conditions, like the microtubule destabilizing drug benomyl. Moreover, cells expressing solely the YEATS domain grow worser than cells expressing any other Taf14 construct tested, including the deletion mutant. Thus, this highly conserved domain should be considered part of a negative regulatory loop in cell growth. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00438-010-0523-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-28395152010-03-26 The YEATS domain of Taf14 in Saccharomyces cerevisiae has a negative impact on cell growth Schulze, Julia M. Kane, Caroline M. Ruiz-Manzano, Ana Mol Genet Genomics Original Paper The role of a highly conserved YEATS protein motif is explored in the context of the Taf14 protein of Saccharomyces cerevisiae. In S. cerevisiae, Taf14 is a protein physically associated with many critical multisubunit complexes including the general transcription factors TFIID and TFIIF, the chromatin remodeling complexes SWI/SNF, Ino80 and RSC, Mediator and the histone modification enzyme NuA3. Taf14 is a member of the YEATS superfamily, conserved from bacteria to eukaryotes and thought to have a transcription stimulatory activity. However, besides its ubiquitous presence and its links with transcription, little is known about Taf14’s role in the nucleus. We use structure–function and mutational analysis to study the function of Taf14 and its well conserved N-terminal YEATS domain. We show here that the YEATS domain is not necessary for Taf14’s association with these transcription and chromatin remodeling complexes, and that its presence in these complexes is dependent only on its C-terminal domain. Our results also indicate that Taf14’s YEATS domain is not necessary for complementing the synthetic lethality between TAF14 and the general transcription factor TFIIS (encoded by DST1). Furthermore, we present evidence that the YEATS domain of Taf14 has a negative impact on cell growth: its absence enables cells to grow better than wild-type cells under stress conditions, like the microtubule destabilizing drug benomyl. Moreover, cells expressing solely the YEATS domain grow worser than cells expressing any other Taf14 construct tested, including the deletion mutant. Thus, this highly conserved domain should be considered part of a negative regulatory loop in cell growth. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00438-010-0523-x) contains supplementary material, which is available to authorized users. Springer-Verlag 2010-02-24 2010 /pmc/articles/PMC2839515/ /pubmed/20179968 http://dx.doi.org/10.1007/s00438-010-0523-x Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Schulze, Julia M.
Kane, Caroline M.
Ruiz-Manzano, Ana
The YEATS domain of Taf14 in Saccharomyces cerevisiae has a negative impact on cell growth
title The YEATS domain of Taf14 in Saccharomyces cerevisiae has a negative impact on cell growth
title_full The YEATS domain of Taf14 in Saccharomyces cerevisiae has a negative impact on cell growth
title_fullStr The YEATS domain of Taf14 in Saccharomyces cerevisiae has a negative impact on cell growth
title_full_unstemmed The YEATS domain of Taf14 in Saccharomyces cerevisiae has a negative impact on cell growth
title_short The YEATS domain of Taf14 in Saccharomyces cerevisiae has a negative impact on cell growth
title_sort yeats domain of taf14 in saccharomyces cerevisiae has a negative impact on cell growth
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839515/
https://www.ncbi.nlm.nih.gov/pubmed/20179968
http://dx.doi.org/10.1007/s00438-010-0523-x
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