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Functional Studies of the Yeast Med5, Med15 and Med16 Mediator Tail Subunits
The yeast Mediator complex can be divided into three modules, designated Head, Middle and Tail. Tail comprises the Med2, Med3, Med5, Med15 and Med16 protein subunits, which are all encoded by genes that are individually non-essential for viability. In cells lacking Med16, Tail is displaced from Head...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750046/ https://www.ncbi.nlm.nih.gov/pubmed/23991176 http://dx.doi.org/10.1371/journal.pone.0073137 |
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author | Larsson, Miriam Uvell, Hanna Sandström, Jenny Rydén, Patrik Selth, Luke A. Björklund, Stefan |
author_facet | Larsson, Miriam Uvell, Hanna Sandström, Jenny Rydén, Patrik Selth, Luke A. Björklund, Stefan |
author_sort | Larsson, Miriam |
collection | PubMed |
description | The yeast Mediator complex can be divided into three modules, designated Head, Middle and Tail. Tail comprises the Med2, Med3, Med5, Med15 and Med16 protein subunits, which are all encoded by genes that are individually non-essential for viability. In cells lacking Med16, Tail is displaced from Head and Middle. However, inactivation of MED5/MED15 and MED15/MED16 are synthetically lethal, indicating that Tail performs essential functions as a separate complex even when it is not bound to Middle and Head. We have used the N-Degron method to create temperature-sensitive (ts) mutants in the Mediator tail subunits Med5, Med15 and Med16 to study the immediate effects on global gene expression when each subunit is individually inactivated, and when Med5/15 or Med15/16 are inactivated together. We identify 25 genes in each double mutant that show a significant change in expression when compared to the corresponding single mutants and to the wild type strain. Importantly, 13 of the 25 identified genes are common for both double mutants. We also find that all strains in which MED15 is inactivated show down-regulation of genes that have been identified as targets for the Ace2 transcriptional activator protein, which is important for progression through the G1 phase of the cell cycle. Supporting this observation, we demonstrate that loss of Med15 leads to a G1 arrest phenotype. Collectively, these findings provide insight into the function of the Mediator Tail module. |
format | Online Article Text |
id | pubmed-3750046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37500462013-08-29 Functional Studies of the Yeast Med5, Med15 and Med16 Mediator Tail Subunits Larsson, Miriam Uvell, Hanna Sandström, Jenny Rydén, Patrik Selth, Luke A. Björklund, Stefan PLoS One Research Article The yeast Mediator complex can be divided into three modules, designated Head, Middle and Tail. Tail comprises the Med2, Med3, Med5, Med15 and Med16 protein subunits, which are all encoded by genes that are individually non-essential for viability. In cells lacking Med16, Tail is displaced from Head and Middle. However, inactivation of MED5/MED15 and MED15/MED16 are synthetically lethal, indicating that Tail performs essential functions as a separate complex even when it is not bound to Middle and Head. We have used the N-Degron method to create temperature-sensitive (ts) mutants in the Mediator tail subunits Med5, Med15 and Med16 to study the immediate effects on global gene expression when each subunit is individually inactivated, and when Med5/15 or Med15/16 are inactivated together. We identify 25 genes in each double mutant that show a significant change in expression when compared to the corresponding single mutants and to the wild type strain. Importantly, 13 of the 25 identified genes are common for both double mutants. We also find that all strains in which MED15 is inactivated show down-regulation of genes that have been identified as targets for the Ace2 transcriptional activator protein, which is important for progression through the G1 phase of the cell cycle. Supporting this observation, we demonstrate that loss of Med15 leads to a G1 arrest phenotype. Collectively, these findings provide insight into the function of the Mediator Tail module. Public Library of Science 2013-08-22 /pmc/articles/PMC3750046/ /pubmed/23991176 http://dx.doi.org/10.1371/journal.pone.0073137 Text en © 2013 Larsson et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Larsson, Miriam Uvell, Hanna Sandström, Jenny Rydén, Patrik Selth, Luke A. Björklund, Stefan Functional Studies of the Yeast Med5, Med15 and Med16 Mediator Tail Subunits |
title | Functional Studies of the Yeast Med5, Med15 and Med16 Mediator Tail Subunits |
title_full | Functional Studies of the Yeast Med5, Med15 and Med16 Mediator Tail Subunits |
title_fullStr | Functional Studies of the Yeast Med5, Med15 and Med16 Mediator Tail Subunits |
title_full_unstemmed | Functional Studies of the Yeast Med5, Med15 and Med16 Mediator Tail Subunits |
title_short | Functional Studies of the Yeast Med5, Med15 and Med16 Mediator Tail Subunits |
title_sort | functional studies of the yeast med5, med15 and med16 mediator tail subunits |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750046/ https://www.ncbi.nlm.nih.gov/pubmed/23991176 http://dx.doi.org/10.1371/journal.pone.0073137 |
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