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Glycogen Synthase Kinase 3 Beta (GSK3β) Phosphorylates the RNAase III Enzyme Drosha at S300 and S302

The canonical microRNA (miRNA) pathway commences with the enzymatic cleavage of the primary gene transcript (pri-miRNA) by the RNAase III enzyme Drosha in the nucleus into shorter pre-miRNA species that are subsequently exported to the cytoplasm for further processing into shorter, mature miRNA mole...

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Detalles Bibliográficos
Autores principales: Tang, Xiaoli, Li, Ming, Tucker, Lynne, Ramratnam, Bharat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108596/
https://www.ncbi.nlm.nih.gov/pubmed/21674040
http://dx.doi.org/10.1371/journal.pone.0020391
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author Tang, Xiaoli
Li, Ming
Tucker, Lynne
Ramratnam, Bharat
author_facet Tang, Xiaoli
Li, Ming
Tucker, Lynne
Ramratnam, Bharat
author_sort Tang, Xiaoli
collection PubMed
description The canonical microRNA (miRNA) pathway commences with the enzymatic cleavage of the primary gene transcript (pri-miRNA) by the RNAase III enzyme Drosha in the nucleus into shorter pre-miRNA species that are subsequently exported to the cytoplasm for further processing into shorter, mature miRNA molecules. Using a series of reporter constructs, we have previously demonstrated that phosphorylation of Drosha at Ser 300 and 302 was required for its nuclear localization. Here, we identify GSK3β as the culprit kinase. We demonstrate that Drosha is unable to selectively localize to the nucleus in cells deficient in GSK3β. These findings expand the substrate base of GSK3β to include a central component of the miRNA biogenesis pathway.
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spelling pubmed-31085962011-06-13 Glycogen Synthase Kinase 3 Beta (GSK3β) Phosphorylates the RNAase III Enzyme Drosha at S300 and S302 Tang, Xiaoli Li, Ming Tucker, Lynne Ramratnam, Bharat PLoS One Research Article The canonical microRNA (miRNA) pathway commences with the enzymatic cleavage of the primary gene transcript (pri-miRNA) by the RNAase III enzyme Drosha in the nucleus into shorter pre-miRNA species that are subsequently exported to the cytoplasm for further processing into shorter, mature miRNA molecules. Using a series of reporter constructs, we have previously demonstrated that phosphorylation of Drosha at Ser 300 and 302 was required for its nuclear localization. Here, we identify GSK3β as the culprit kinase. We demonstrate that Drosha is unable to selectively localize to the nucleus in cells deficient in GSK3β. These findings expand the substrate base of GSK3β to include a central component of the miRNA biogenesis pathway. Public Library of Science 2011-06-03 /pmc/articles/PMC3108596/ /pubmed/21674040 http://dx.doi.org/10.1371/journal.pone.0020391 Text en Tang 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
Tang, Xiaoli
Li, Ming
Tucker, Lynne
Ramratnam, Bharat
Glycogen Synthase Kinase 3 Beta (GSK3β) Phosphorylates the RNAase III Enzyme Drosha at S300 and S302
title Glycogen Synthase Kinase 3 Beta (GSK3β) Phosphorylates the RNAase III Enzyme Drosha at S300 and S302
title_full Glycogen Synthase Kinase 3 Beta (GSK3β) Phosphorylates the RNAase III Enzyme Drosha at S300 and S302
title_fullStr Glycogen Synthase Kinase 3 Beta (GSK3β) Phosphorylates the RNAase III Enzyme Drosha at S300 and S302
title_full_unstemmed Glycogen Synthase Kinase 3 Beta (GSK3β) Phosphorylates the RNAase III Enzyme Drosha at S300 and S302
title_short Glycogen Synthase Kinase 3 Beta (GSK3β) Phosphorylates the RNAase III Enzyme Drosha at S300 and S302
title_sort glycogen synthase kinase 3 beta (gsk3β) phosphorylates the rnaase iii enzyme drosha at s300 and s302
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108596/
https://www.ncbi.nlm.nih.gov/pubmed/21674040
http://dx.doi.org/10.1371/journal.pone.0020391
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