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ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes
Upon pathogen detection, the innate immune system triggers signaling events leading to upregulation of pro-inflammatory and anti-microbial mRNA transcripts. RNA-binding proteins (RBPs) interact with these critical mRNAs and regulate their fates at the post-transcriptional level. One such RBP is ELAV...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225249/ https://www.ncbi.nlm.nih.gov/pubmed/34038724 http://dx.doi.org/10.1016/j.celrep.2021.109178 |
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author | Rothamel, Katherine Arcos, Sarah Kim, Byungil Reasoner, Clara Lisy, Samantha Mukherjee, Neelanjan Ascano, Manuel |
author_facet | Rothamel, Katherine Arcos, Sarah Kim, Byungil Reasoner, Clara Lisy, Samantha Mukherjee, Neelanjan Ascano, Manuel |
author_sort | Rothamel, Katherine |
collection | PubMed |
description | Upon pathogen detection, the innate immune system triggers signaling events leading to upregulation of pro-inflammatory and anti-microbial mRNA transcripts. RNA-binding proteins (RBPs) interact with these critical mRNAs and regulate their fates at the post-transcriptional level. One such RBP is ELAVL1. Although significant progress has been made in understanding how embryonic lethal vision-like protein 1 (ELAVL1) regulates mRNAs, its target repertoire and binding distribution within an immunological context remain poorly understood. We overlap four high-throughput approaches to define its context-dependent targets and determine its regulatory impact during immune activation. ELAVL1 transitions from binding overwhelmingly intronic sites to 3′ UTR sites upon immune stimulation of cells, binding previously and newly expressed mRNAs. We find that ELAVL1 mediates the RNA stability of genes that regulate pathways essential to pathogen sensing and cytokine production. Our findings reveal the importance of examining RBP regulatory impact under dynamic transcriptomic events to understand their post-transcriptional regulatory roles within specific biological circuitries. |
format | Online Article Text |
id | pubmed-8225249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-82252492021-06-24 ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes Rothamel, Katherine Arcos, Sarah Kim, Byungil Reasoner, Clara Lisy, Samantha Mukherjee, Neelanjan Ascano, Manuel Cell Rep Article Upon pathogen detection, the innate immune system triggers signaling events leading to upregulation of pro-inflammatory and anti-microbial mRNA transcripts. RNA-binding proteins (RBPs) interact with these critical mRNAs and regulate their fates at the post-transcriptional level. One such RBP is ELAVL1. Although significant progress has been made in understanding how embryonic lethal vision-like protein 1 (ELAVL1) regulates mRNAs, its target repertoire and binding distribution within an immunological context remain poorly understood. We overlap four high-throughput approaches to define its context-dependent targets and determine its regulatory impact during immune activation. ELAVL1 transitions from binding overwhelmingly intronic sites to 3′ UTR sites upon immune stimulation of cells, binding previously and newly expressed mRNAs. We find that ELAVL1 mediates the RNA stability of genes that regulate pathways essential to pathogen sensing and cytokine production. Our findings reveal the importance of examining RBP regulatory impact under dynamic transcriptomic events to understand their post-transcriptional regulatory roles within specific biological circuitries. 2021-05-25 /pmc/articles/PMC8225249/ /pubmed/34038724 http://dx.doi.org/10.1016/j.celrep.2021.109178 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Rothamel, Katherine Arcos, Sarah Kim, Byungil Reasoner, Clara Lisy, Samantha Mukherjee, Neelanjan Ascano, Manuel ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes |
title | ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes |
title_full | ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes |
title_fullStr | ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes |
title_full_unstemmed | ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes |
title_short | ELAVL1 primarily couples mRNA stability with the 3′ UTRs of interferon-stimulated genes |
title_sort | elavl1 primarily couples mrna stability with the 3′ utrs of interferon-stimulated genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225249/ https://www.ncbi.nlm.nih.gov/pubmed/34038724 http://dx.doi.org/10.1016/j.celrep.2021.109178 |
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