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Environmental perturbations lead to extensive directional shifts in RNA processing
Environmental perturbations have large effects on both organismal and cellular traits, including gene expression, but the extent to which the environment affects RNA processing remains largely uncharacterized. Recent studies have identified a large number of genetic variants associated with variatio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667937/ https://www.ncbi.nlm.nih.gov/pubmed/29023442 http://dx.doi.org/10.1371/journal.pgen.1006995 |
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author | Richards, Allison L. Watza, Donovan Findley, Anthony Alazizi, Adnan Wen, Xiaoquan Pai, Athma A. Pique-Regi, Roger Luca, Francesca |
author_facet | Richards, Allison L. Watza, Donovan Findley, Anthony Alazizi, Adnan Wen, Xiaoquan Pai, Athma A. Pique-Regi, Roger Luca, Francesca |
author_sort | Richards, Allison L. |
collection | PubMed |
description | Environmental perturbations have large effects on both organismal and cellular traits, including gene expression, but the extent to which the environment affects RNA processing remains largely uncharacterized. Recent studies have identified a large number of genetic variants associated with variation in RNA processing that also have an important role in complex traits; yet we do not know in which contexts the different underlying isoforms are used. Here, we comprehensively characterized changes in RNA processing events across 89 environments in five human cell types and identified 15,300 event shifts (FDR = 15%) comprised of eight event types in over 4,000 genes. Many of these changes occur consistently in the same direction across conditions, indicative of global regulation by trans factors. Accordingly, we demonstrate that environmental modulation of splicing factor binding predicts shifts in intron retention, and that binding of transcription factors predicts shifts in alternative first exon (AFE) usage in response to specific treatments. We validated the mechanism hypothesized for AFE in two independent datasets. Using ATAC-seq, we found altered binding of 64 factors in response to selenium at sites of AFE shift, including ELF2 and other factors in the ETS family. We also performed AFE QTL mapping in 373 individuals and found an enrichment for SNPs predicted to disrupt binding of the ELF2 factor. Together, these results demonstrate that RNA processing is dramatically changed in response to environmental perturbations through specific mechanisms regulated by trans factors. |
format | Online Article Text |
id | pubmed-5667937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56679372017-11-18 Environmental perturbations lead to extensive directional shifts in RNA processing Richards, Allison L. Watza, Donovan Findley, Anthony Alazizi, Adnan Wen, Xiaoquan Pai, Athma A. Pique-Regi, Roger Luca, Francesca PLoS Genet Research Article Environmental perturbations have large effects on both organismal and cellular traits, including gene expression, but the extent to which the environment affects RNA processing remains largely uncharacterized. Recent studies have identified a large number of genetic variants associated with variation in RNA processing that also have an important role in complex traits; yet we do not know in which contexts the different underlying isoforms are used. Here, we comprehensively characterized changes in RNA processing events across 89 environments in five human cell types and identified 15,300 event shifts (FDR = 15%) comprised of eight event types in over 4,000 genes. Many of these changes occur consistently in the same direction across conditions, indicative of global regulation by trans factors. Accordingly, we demonstrate that environmental modulation of splicing factor binding predicts shifts in intron retention, and that binding of transcription factors predicts shifts in alternative first exon (AFE) usage in response to specific treatments. We validated the mechanism hypothesized for AFE in two independent datasets. Using ATAC-seq, we found altered binding of 64 factors in response to selenium at sites of AFE shift, including ELF2 and other factors in the ETS family. We also performed AFE QTL mapping in 373 individuals and found an enrichment for SNPs predicted to disrupt binding of the ELF2 factor. Together, these results demonstrate that RNA processing is dramatically changed in response to environmental perturbations through specific mechanisms regulated by trans factors. Public Library of Science 2017-10-12 /pmc/articles/PMC5667937/ /pubmed/29023442 http://dx.doi.org/10.1371/journal.pgen.1006995 Text en © 2017 Richards 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Richards, Allison L. Watza, Donovan Findley, Anthony Alazizi, Adnan Wen, Xiaoquan Pai, Athma A. Pique-Regi, Roger Luca, Francesca Environmental perturbations lead to extensive directional shifts in RNA processing |
title | Environmental perturbations lead to extensive directional shifts in RNA processing |
title_full | Environmental perturbations lead to extensive directional shifts in RNA processing |
title_fullStr | Environmental perturbations lead to extensive directional shifts in RNA processing |
title_full_unstemmed | Environmental perturbations lead to extensive directional shifts in RNA processing |
title_short | Environmental perturbations lead to extensive directional shifts in RNA processing |
title_sort | environmental perturbations lead to extensive directional shifts in rna processing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667937/ https://www.ncbi.nlm.nih.gov/pubmed/29023442 http://dx.doi.org/10.1371/journal.pgen.1006995 |
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