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HSP90 Protein Stabilizes Unloaded Argonaute Complexes and Microscopic P-bodies in Human Cells

Key components of the miRNA-mediated gene regulation pathway are localized in cytoplasmic processing bodies (P-bodies). Mounting evidence suggests that the presence of microscopic P-bodies are not always required for miRNA-mediated gene regulation. Here we have shown that geldanamycin, a well-charac...

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Detalles Bibliográficos
Autores principales: Johnston, Michael, Geoffroy, Marie-Claude, Sobala, Andrew, Hay, Ron, Hutvagner, Gyorgy
Formato: Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861606/
https://www.ncbi.nlm.nih.gov/pubmed/20237157
http://dx.doi.org/10.1091/mbc.E09-10-0885
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author Johnston, Michael
Geoffroy, Marie-Claude
Sobala, Andrew
Hay, Ron
Hutvagner, Gyorgy
author_facet Johnston, Michael
Geoffroy, Marie-Claude
Sobala, Andrew
Hay, Ron
Hutvagner, Gyorgy
author_sort Johnston, Michael
collection PubMed
description Key components of the miRNA-mediated gene regulation pathway are localized in cytoplasmic processing bodies (P-bodies). Mounting evidence suggests that the presence of microscopic P-bodies are not always required for miRNA-mediated gene regulation. Here we have shown that geldanamycin, a well-characterized HSP90 inhibitor, abolishes P-bodies and significantly reduces Argonaute and GW182 protein levels but does not affect the miRNA level and the efficiency of miRNA-mediated gene repression; however, it significantly impairs siRNA loading and the efficacy of exogenous siRNA. Our data suggests that HSP90 protein chaperones Argonautes before binding RNA and may facilitate efficient loading of small RNA.
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spelling pubmed-28616062010-07-16 HSP90 Protein Stabilizes Unloaded Argonaute Complexes and Microscopic P-bodies in Human Cells Johnston, Michael Geoffroy, Marie-Claude Sobala, Andrew Hay, Ron Hutvagner, Gyorgy Mol Biol Cell Articles Key components of the miRNA-mediated gene regulation pathway are localized in cytoplasmic processing bodies (P-bodies). Mounting evidence suggests that the presence of microscopic P-bodies are not always required for miRNA-mediated gene regulation. Here we have shown that geldanamycin, a well-characterized HSP90 inhibitor, abolishes P-bodies and significantly reduces Argonaute and GW182 protein levels but does not affect the miRNA level and the efficiency of miRNA-mediated gene repression; however, it significantly impairs siRNA loading and the efficacy of exogenous siRNA. Our data suggests that HSP90 protein chaperones Argonautes before binding RNA and may facilitate efficient loading of small RNA. The American Society for Cell Biology 2010-05-01 /pmc/articles/PMC2861606/ /pubmed/20237157 http://dx.doi.org/10.1091/mbc.E09-10-0885 Text en © 2010 by The American Society for Cell Biology
spellingShingle Articles
Johnston, Michael
Geoffroy, Marie-Claude
Sobala, Andrew
Hay, Ron
Hutvagner, Gyorgy
HSP90 Protein Stabilizes Unloaded Argonaute Complexes and Microscopic P-bodies in Human Cells
title HSP90 Protein Stabilizes Unloaded Argonaute Complexes and Microscopic P-bodies in Human Cells
title_full HSP90 Protein Stabilizes Unloaded Argonaute Complexes and Microscopic P-bodies in Human Cells
title_fullStr HSP90 Protein Stabilizes Unloaded Argonaute Complexes and Microscopic P-bodies in Human Cells
title_full_unstemmed HSP90 Protein Stabilizes Unloaded Argonaute Complexes and Microscopic P-bodies in Human Cells
title_short HSP90 Protein Stabilizes Unloaded Argonaute Complexes and Microscopic P-bodies in Human Cells
title_sort hsp90 protein stabilizes unloaded argonaute complexes and microscopic p-bodies in human cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861606/
https://www.ncbi.nlm.nih.gov/pubmed/20237157
http://dx.doi.org/10.1091/mbc.E09-10-0885
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