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Importin-β facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels
MicroRNAs (miRNAs) guide Argonaute (Ago) proteins to distinct target mRNAs leading to translational repression and mRNA decay. Ago proteins interact with a member of the GW protein family, referred to as TNRC6A-C in mammals, which coordinate downstream gene-silencing processes. The cytoplasmic funct...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551936/ https://www.ncbi.nlm.nih.gov/pubmed/26170235 http://dx.doi.org/10.1093/nar/gkv705 |
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author | Schraivogel, Daniel Schindler, Susann G. Danner, Johannes Kremmer, Elisabeth Pfaff, Janina Hannus, Stefan Depping, Reinhard Meister, Gunter |
author_facet | Schraivogel, Daniel Schindler, Susann G. Danner, Johannes Kremmer, Elisabeth Pfaff, Janina Hannus, Stefan Depping, Reinhard Meister, Gunter |
author_sort | Schraivogel, Daniel |
collection | PubMed |
description | MicroRNAs (miRNAs) guide Argonaute (Ago) proteins to distinct target mRNAs leading to translational repression and mRNA decay. Ago proteins interact with a member of the GW protein family, referred to as TNRC6A-C in mammals, which coordinate downstream gene-silencing processes. The cytoplasmic functions of TNRC6 and Ago proteins are reasonably well established. Both protein families are found in the nucleus as well. Their detailed nuclear functions, however, remain elusive. Furthermore, it is not clear which import routes Ago and TNRC6 proteins take into the nucleus. Using different nuclear transport assays, we find that Ago as well as TNRC6 proteins shuttle between the cytoplasm and the nucleus. While import receptors might function redundantly to transport Ago2, we demonstrate that TNRC6 proteins are imported by the Importin-β pathway. Finally, we show that nuclear localization of both Ago2 and TNRC6 proteins can depend on each other suggesting actively balanced cytoplasmic Ago – TNRC6 levels. |
format | Online Article Text |
id | pubmed-4551936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45519362015-08-28 Importin-β facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels Schraivogel, Daniel Schindler, Susann G. Danner, Johannes Kremmer, Elisabeth Pfaff, Janina Hannus, Stefan Depping, Reinhard Meister, Gunter Nucleic Acids Res Molecular Biology MicroRNAs (miRNAs) guide Argonaute (Ago) proteins to distinct target mRNAs leading to translational repression and mRNA decay. Ago proteins interact with a member of the GW protein family, referred to as TNRC6A-C in mammals, which coordinate downstream gene-silencing processes. The cytoplasmic functions of TNRC6 and Ago proteins are reasonably well established. Both protein families are found in the nucleus as well. Their detailed nuclear functions, however, remain elusive. Furthermore, it is not clear which import routes Ago and TNRC6 proteins take into the nucleus. Using different nuclear transport assays, we find that Ago as well as TNRC6 proteins shuttle between the cytoplasm and the nucleus. While import receptors might function redundantly to transport Ago2, we demonstrate that TNRC6 proteins are imported by the Importin-β pathway. Finally, we show that nuclear localization of both Ago2 and TNRC6 proteins can depend on each other suggesting actively balanced cytoplasmic Ago – TNRC6 levels. Oxford University Press 2015-09-03 2015-07-13 /pmc/articles/PMC4551936/ /pubmed/26170235 http://dx.doi.org/10.1093/nar/gkv705 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Molecular Biology Schraivogel, Daniel Schindler, Susann G. Danner, Johannes Kremmer, Elisabeth Pfaff, Janina Hannus, Stefan Depping, Reinhard Meister, Gunter Importin-β facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels |
title | Importin-β facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels |
title_full | Importin-β facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels |
title_fullStr | Importin-β facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels |
title_full_unstemmed | Importin-β facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels |
title_short | Importin-β facilitates nuclear import of human GW proteins and balances cytoplasmic gene silencing protein levels |
title_sort | importin-β facilitates nuclear import of human gw proteins and balances cytoplasmic gene silencing protein levels |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551936/ https://www.ncbi.nlm.nih.gov/pubmed/26170235 http://dx.doi.org/10.1093/nar/gkv705 |
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