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KH domain containing RNA-binding proteins coordinate with microRNAs to regulate Caenorhabditis elegans development
MicroRNAs (miRNAs) and RNA-binding proteins (RBPs) regulate gene expression at the post-transcriptional level, but the extent to which these key regulators of gene expression coordinate their activities and the precise mechanisms of this coordination are not well understood. RBPs often have recogniz...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022929/ https://www.ncbi.nlm.nih.gov/pubmed/33585875 http://dx.doi.org/10.1093/g3journal/jkab013 |
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author | Haskell, Dustin Zinovyeva, Anna |
author_facet | Haskell, Dustin Zinovyeva, Anna |
author_sort | Haskell, Dustin |
collection | PubMed |
description | MicroRNAs (miRNAs) and RNA-binding proteins (RBPs) regulate gene expression at the post-transcriptional level, but the extent to which these key regulators of gene expression coordinate their activities and the precise mechanisms of this coordination are not well understood. RBPs often have recognizable RNA binding domains that correlate with specific protein function. Recently, several RBPs containing K homology (KH) RNA binding domains were shown to work with miRNAs to regulate gene expression, raising the possibility that KH domains may be important for coordinating with miRNA pathways in gene expression regulation. To ascertain whether additional KH domain proteins functionally interact with miRNAs during Caenorhabditis elegans development, we knocked down twenty-four genes encoding KH-domain proteins in several miRNA sensitized genetic backgrounds. Here, we report that a majority of the KH domain-containing genes genetically interact with multiple miRNAs and Argonaute alg-1. Interestingly, two KH domain genes, predicted splicing factors sfa-1 and asd-2, genetically interacted with all of the miRNA mutants tested, whereas other KH domain genes showed genetic interactions only with specific miRNAs. Our domain architecture and phylogenetic relationship analyses of the C. elegans KH domain-containing proteins revealed potential groups that may share both structure and function. Collectively, we show that many C. elegans KH domain RBPs functionally interact with miRNAs, suggesting direct or indirect coordination between these two classes of post-transcriptional gene expression regulators. |
format | Online Article Text |
id | pubmed-8022929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80229292021-04-09 KH domain containing RNA-binding proteins coordinate with microRNAs to regulate Caenorhabditis elegans development Haskell, Dustin Zinovyeva, Anna G3 (Bethesda) Investigation MicroRNAs (miRNAs) and RNA-binding proteins (RBPs) regulate gene expression at the post-transcriptional level, but the extent to which these key regulators of gene expression coordinate their activities and the precise mechanisms of this coordination are not well understood. RBPs often have recognizable RNA binding domains that correlate with specific protein function. Recently, several RBPs containing K homology (KH) RNA binding domains were shown to work with miRNAs to regulate gene expression, raising the possibility that KH domains may be important for coordinating with miRNA pathways in gene expression regulation. To ascertain whether additional KH domain proteins functionally interact with miRNAs during Caenorhabditis elegans development, we knocked down twenty-four genes encoding KH-domain proteins in several miRNA sensitized genetic backgrounds. Here, we report that a majority of the KH domain-containing genes genetically interact with multiple miRNAs and Argonaute alg-1. Interestingly, two KH domain genes, predicted splicing factors sfa-1 and asd-2, genetically interacted with all of the miRNA mutants tested, whereas other KH domain genes showed genetic interactions only with specific miRNAs. Our domain architecture and phylogenetic relationship analyses of the C. elegans KH domain-containing proteins revealed potential groups that may share both structure and function. Collectively, we show that many C. elegans KH domain RBPs functionally interact with miRNAs, suggesting direct or indirect coordination between these two classes of post-transcriptional gene expression regulators. Oxford University Press 2021-01-23 /pmc/articles/PMC8022929/ /pubmed/33585875 http://dx.doi.org/10.1093/g3journal/jkab013 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigation Haskell, Dustin Zinovyeva, Anna KH domain containing RNA-binding proteins coordinate with microRNAs to regulate Caenorhabditis elegans development |
title | KH domain containing RNA-binding proteins coordinate with microRNAs to regulate Caenorhabditis elegans development |
title_full | KH domain containing RNA-binding proteins coordinate with microRNAs to regulate Caenorhabditis elegans development |
title_fullStr | KH domain containing RNA-binding proteins coordinate with microRNAs to regulate Caenorhabditis elegans development |
title_full_unstemmed | KH domain containing RNA-binding proteins coordinate with microRNAs to regulate Caenorhabditis elegans development |
title_short | KH domain containing RNA-binding proteins coordinate with microRNAs to regulate Caenorhabditis elegans development |
title_sort | kh domain containing rna-binding proteins coordinate with micrornas to regulate caenorhabditis elegans development |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022929/ https://www.ncbi.nlm.nih.gov/pubmed/33585875 http://dx.doi.org/10.1093/g3journal/jkab013 |
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