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Auto- and cross-regulation of the hnRNPs D and DL

HnRNP D, better known as AUF1, is an extensively studied protein that controls a variety of cellular pathways. Consequently, its expression has to be tightly regulated to prevent the onset of pathologies. In contrast, the cellular functions and regulation of its ubiquitously expressed paralog hnRNP...

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Detalles Bibliográficos
Autores principales: Kemmerer, Katrin, Fischer, Sandra, Weigand, Julia E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824352/
https://www.ncbi.nlm.nih.gov/pubmed/29263134
http://dx.doi.org/10.1261/rna.063420.117
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author Kemmerer, Katrin
Fischer, Sandra
Weigand, Julia E.
author_facet Kemmerer, Katrin
Fischer, Sandra
Weigand, Julia E.
author_sort Kemmerer, Katrin
collection PubMed
description HnRNP D, better known as AUF1, is an extensively studied protein that controls a variety of cellular pathways. Consequently, its expression has to be tightly regulated to prevent the onset of pathologies. In contrast, the cellular functions and regulation of its ubiquitously expressed paralog hnRNP DL are barely explored. Here, we present an intricate crosstalk between these two proteins. Both hnRNP D and DL are able to control their own expression by alternative splicing of cassette exons in their 3′UTRs. Exon inclusion produces mRNAs degraded by nonsense-mediated decay. Moreover, hnRNP D and DL control the expression of one another by the same mechanism. Thus, we identified two novel ways of how hnRNP D expression is controlled. The tight interconnection of expression control directly links hnRNP DL to hnRNP D-related diseases and emphasizes the importance of a systematic analysis of its cellular functions.
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spelling pubmed-58243522019-03-01 Auto- and cross-regulation of the hnRNPs D and DL Kemmerer, Katrin Fischer, Sandra Weigand, Julia E. RNA Report HnRNP D, better known as AUF1, is an extensively studied protein that controls a variety of cellular pathways. Consequently, its expression has to be tightly regulated to prevent the onset of pathologies. In contrast, the cellular functions and regulation of its ubiquitously expressed paralog hnRNP DL are barely explored. Here, we present an intricate crosstalk between these two proteins. Both hnRNP D and DL are able to control their own expression by alternative splicing of cassette exons in their 3′UTRs. Exon inclusion produces mRNAs degraded by nonsense-mediated decay. Moreover, hnRNP D and DL control the expression of one another by the same mechanism. Thus, we identified two novel ways of how hnRNP D expression is controlled. The tight interconnection of expression control directly links hnRNP DL to hnRNP D-related diseases and emphasizes the importance of a systematic analysis of its cellular functions. Cold Spring Harbor Laboratory Press 2018-03 /pmc/articles/PMC5824352/ /pubmed/29263134 http://dx.doi.org/10.1261/rna.063420.117 Text en © 2018 Kemmerer et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Report
Kemmerer, Katrin
Fischer, Sandra
Weigand, Julia E.
Auto- and cross-regulation of the hnRNPs D and DL
title Auto- and cross-regulation of the hnRNPs D and DL
title_full Auto- and cross-regulation of the hnRNPs D and DL
title_fullStr Auto- and cross-regulation of the hnRNPs D and DL
title_full_unstemmed Auto- and cross-regulation of the hnRNPs D and DL
title_short Auto- and cross-regulation of the hnRNPs D and DL
title_sort auto- and cross-regulation of the hnrnps d and dl
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824352/
https://www.ncbi.nlm.nih.gov/pubmed/29263134
http://dx.doi.org/10.1261/rna.063420.117
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