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Yeast Gis2 and Its Human Ortholog CNBP Are Novel Components of Stress-Induced RNP Granules
Although a CCTG expansion in the gene encoding the zinc knuckle protein CNBP causes a common form of muscular dystrophy, the function of both human CNBP and its putative budding yeast ortholog Gis2 remain poorly understood. Here we report the protein interactions of Gis2 and the subcellular location...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528734/ https://www.ncbi.nlm.nih.gov/pubmed/23285195 http://dx.doi.org/10.1371/journal.pone.0052824 |
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author | Rojas, Marta Farr, George W. Fernandez, Cesar F. Lauden, Laura McCormack, John C. Wolin, Sandra L. |
author_facet | Rojas, Marta Farr, George W. Fernandez, Cesar F. Lauden, Laura McCormack, John C. Wolin, Sandra L. |
author_sort | Rojas, Marta |
collection | PubMed |
description | Although a CCTG expansion in the gene encoding the zinc knuckle protein CNBP causes a common form of muscular dystrophy, the function of both human CNBP and its putative budding yeast ortholog Gis2 remain poorly understood. Here we report the protein interactions of Gis2 and the subcellular locations of both Gis2 and CNBP. We found that Gis2 exhibits RNA-dependent interactions with two proteins involved in mRNA recognition, the poly(A) binding protein and the translation initiation factor eIF4G. We show that Gis2 is a component of two large RNA-protein granules, processing bodies and stress granules, which contain translationally repressed mRNAs. Consistent with a functional ortholog, CNBP also associates with the poly(A) binding protein and accumulates in stress granules during arsenite treatment of human cells. These results implicate both Gis2 and CNBP in mRNA handling during stress. |
format | Online Article Text |
id | pubmed-3528734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35287342013-01-02 Yeast Gis2 and Its Human Ortholog CNBP Are Novel Components of Stress-Induced RNP Granules Rojas, Marta Farr, George W. Fernandez, Cesar F. Lauden, Laura McCormack, John C. Wolin, Sandra L. PLoS One Research Article Although a CCTG expansion in the gene encoding the zinc knuckle protein CNBP causes a common form of muscular dystrophy, the function of both human CNBP and its putative budding yeast ortholog Gis2 remain poorly understood. Here we report the protein interactions of Gis2 and the subcellular locations of both Gis2 and CNBP. We found that Gis2 exhibits RNA-dependent interactions with two proteins involved in mRNA recognition, the poly(A) binding protein and the translation initiation factor eIF4G. We show that Gis2 is a component of two large RNA-protein granules, processing bodies and stress granules, which contain translationally repressed mRNAs. Consistent with a functional ortholog, CNBP also associates with the poly(A) binding protein and accumulates in stress granules during arsenite treatment of human cells. These results implicate both Gis2 and CNBP in mRNA handling during stress. Public Library of Science 2012-12-21 /pmc/articles/PMC3528734/ /pubmed/23285195 http://dx.doi.org/10.1371/journal.pone.0052824 Text en © 2012 Rojas 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rojas, Marta Farr, George W. Fernandez, Cesar F. Lauden, Laura McCormack, John C. Wolin, Sandra L. Yeast Gis2 and Its Human Ortholog CNBP Are Novel Components of Stress-Induced RNP Granules |
title | Yeast Gis2 and Its Human Ortholog CNBP Are Novel Components of Stress-Induced RNP Granules |
title_full | Yeast Gis2 and Its Human Ortholog CNBP Are Novel Components of Stress-Induced RNP Granules |
title_fullStr | Yeast Gis2 and Its Human Ortholog CNBP Are Novel Components of Stress-Induced RNP Granules |
title_full_unstemmed | Yeast Gis2 and Its Human Ortholog CNBP Are Novel Components of Stress-Induced RNP Granules |
title_short | Yeast Gis2 and Its Human Ortholog CNBP Are Novel Components of Stress-Induced RNP Granules |
title_sort | yeast gis2 and its human ortholog cnbp are novel components of stress-induced rnp granules |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528734/ https://www.ncbi.nlm.nih.gov/pubmed/23285195 http://dx.doi.org/10.1371/journal.pone.0052824 |
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