Cargando…

Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA

Deletions within genes coding for subunits of the transcription coactivator SAGA caused strong genome-wide defects in transcription and SAGA-mediated chromatin modifications. In contrast, rapid SAGA depletion produced only modest transcription defects at 13% of protein-coding genes – genes that are...

Descripción completa

Detalles Bibliográficos
Autores principales: Donczew, Rafal, Warfield, Linda, Pacheco, Derek, Erijman, Ariel, Hahn, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977968/
https://www.ncbi.nlm.nih.gov/pubmed/31913117
http://dx.doi.org/10.7554/eLife.50109
_version_ 1783490615411998720
author Donczew, Rafal
Warfield, Linda
Pacheco, Derek
Erijman, Ariel
Hahn, Steven
author_facet Donczew, Rafal
Warfield, Linda
Pacheco, Derek
Erijman, Ariel
Hahn, Steven
author_sort Donczew, Rafal
collection PubMed
description Deletions within genes coding for subunits of the transcription coactivator SAGA caused strong genome-wide defects in transcription and SAGA-mediated chromatin modifications. In contrast, rapid SAGA depletion produced only modest transcription defects at 13% of protein-coding genes – genes that are generally more sensitive to rapid TFIID depletion. However, transcription of these ‘coactivator-redundant’ genes is strongly affected by rapid depletion of both factors, showing the overlapping functions of TFIID and SAGA at this gene set. We suggest that this overlapping function is linked to TBP-DNA recruitment. The remaining 87% of expressed genes that we term ‘TFIID-dependent’ are highly sensitive to rapid TFIID depletion and insensitive to rapid SAGA depletion. Genome-wide mapping of SAGA and TFIID found binding of both factors at many genes independent of gene class. Promoter analysis suggests that the distinction between the gene classes is due to multiple components rather than any single regulatory factor or promoter sequence motif.
format Online
Article
Text
id pubmed-6977968
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-69779682020-01-27 Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA Donczew, Rafal Warfield, Linda Pacheco, Derek Erijman, Ariel Hahn, Steven eLife Chromosomes and Gene Expression Deletions within genes coding for subunits of the transcription coactivator SAGA caused strong genome-wide defects in transcription and SAGA-mediated chromatin modifications. In contrast, rapid SAGA depletion produced only modest transcription defects at 13% of protein-coding genes – genes that are generally more sensitive to rapid TFIID depletion. However, transcription of these ‘coactivator-redundant’ genes is strongly affected by rapid depletion of both factors, showing the overlapping functions of TFIID and SAGA at this gene set. We suggest that this overlapping function is linked to TBP-DNA recruitment. The remaining 87% of expressed genes that we term ‘TFIID-dependent’ are highly sensitive to rapid TFIID depletion and insensitive to rapid SAGA depletion. Genome-wide mapping of SAGA and TFIID found binding of both factors at many genes independent of gene class. Promoter analysis suggests that the distinction between the gene classes is due to multiple components rather than any single regulatory factor or promoter sequence motif. eLife Sciences Publications, Ltd 2020-01-08 /pmc/articles/PMC6977968/ /pubmed/31913117 http://dx.doi.org/10.7554/eLife.50109 Text en © 2020, Donczew et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Chromosomes and Gene Expression
Donczew, Rafal
Warfield, Linda
Pacheco, Derek
Erijman, Ariel
Hahn, Steven
Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA
title Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA
title_full Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA
title_fullStr Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA
title_full_unstemmed Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA
title_short Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA
title_sort two roles for the yeast transcription coactivator saga and a set of genes redundantly regulated by tfiid and saga
topic Chromosomes and Gene Expression
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977968/
https://www.ncbi.nlm.nih.gov/pubmed/31913117
http://dx.doi.org/10.7554/eLife.50109
work_keys_str_mv AT donczewrafal tworolesfortheyeasttranscriptioncoactivatorsagaandasetofgenesredundantlyregulatedbytfiidandsaga
AT warfieldlinda tworolesfortheyeasttranscriptioncoactivatorsagaandasetofgenesredundantlyregulatedbytfiidandsaga
AT pachecoderek tworolesfortheyeasttranscriptioncoactivatorsagaandasetofgenesredundantlyregulatedbytfiidandsaga
AT erijmanariel tworolesfortheyeasttranscriptioncoactivatorsagaandasetofgenesredundantlyregulatedbytfiidandsaga
AT hahnsteven tworolesfortheyeasttranscriptioncoactivatorsagaandasetofgenesredundantlyregulatedbytfiidandsaga