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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2010
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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. |
format | Text |
id | pubmed-2861606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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