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Antagonistic role of hnRNP A1 and KSRP in the regulation of Let-7a biogenesis

The pluripotency promoting proteins Lin28a and Lin28b act as posttranscriptional repressors of let-7 miRNA biogenesis in undifferentiated embryonic stem cells. The levels of mature let-7a differ substantially in cells lacking Lin28 expression, indicating the existence of additional mechanism(s) of p...

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Detalles Bibliográficos
Autores principales: Michlewski, Gracjan, Cáceres, Javier F.
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923024/
https://www.ncbi.nlm.nih.gov/pubmed/20639884
http://dx.doi.org/10.1038/nsmb.1874
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author Michlewski, Gracjan
Cáceres, Javier F.
author_facet Michlewski, Gracjan
Cáceres, Javier F.
author_sort Michlewski, Gracjan
collection PubMed
description The pluripotency promoting proteins Lin28a and Lin28b act as posttranscriptional repressors of let-7 miRNA biogenesis in undifferentiated embryonic stem cells. The levels of mature let-7a differ substantially in cells lacking Lin28 expression, indicating the existence of additional mechanism(s) of posttranscriptional regulation. Here, we present evidence supporting a role for hnRNP A1 as a negative regulator of let-7a. HnRNP A1 binds the conserved terminal loop of pri-let-7a-1 and inhibits its processing by Drosha. Levels of mature let-7a negatively correlate with hnRNP A1 levels in somatic cell lines. Furthermore, hnRNP A1 depletion increased pri-let-7a-1 processing by cell extracts, whereas its ectopic expression decreased let-7a production in vivo. Finally, hnRNP A1 binding to let-7a interferes with the binding of the KH-type splicing regulatory protein KSRP, known to promote let-7a biogenesis. We propose that hnRNP A1 and KSRP play antagonistic roles in the posttranscriptional regulation of let-7a expression.
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spelling pubmed-29230242011-02-01 Antagonistic role of hnRNP A1 and KSRP in the regulation of Let-7a biogenesis Michlewski, Gracjan Cáceres, Javier F. Nat Struct Mol Biol Article The pluripotency promoting proteins Lin28a and Lin28b act as posttranscriptional repressors of let-7 miRNA biogenesis in undifferentiated embryonic stem cells. The levels of mature let-7a differ substantially in cells lacking Lin28 expression, indicating the existence of additional mechanism(s) of posttranscriptional regulation. Here, we present evidence supporting a role for hnRNP A1 as a negative regulator of let-7a. HnRNP A1 binds the conserved terminal loop of pri-let-7a-1 and inhibits its processing by Drosha. Levels of mature let-7a negatively correlate with hnRNP A1 levels in somatic cell lines. Furthermore, hnRNP A1 depletion increased pri-let-7a-1 processing by cell extracts, whereas its ectopic expression decreased let-7a production in vivo. Finally, hnRNP A1 binding to let-7a interferes with the binding of the KH-type splicing regulatory protein KSRP, known to promote let-7a biogenesis. We propose that hnRNP A1 and KSRP play antagonistic roles in the posttranscriptional regulation of let-7a expression. 2010-07-18 2010-08 /pmc/articles/PMC2923024/ /pubmed/20639884 http://dx.doi.org/10.1038/nsmb.1874 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Michlewski, Gracjan
Cáceres, Javier F.
Antagonistic role of hnRNP A1 and KSRP in the regulation of Let-7a biogenesis
title Antagonistic role of hnRNP A1 and KSRP in the regulation of Let-7a biogenesis
title_full Antagonistic role of hnRNP A1 and KSRP in the regulation of Let-7a biogenesis
title_fullStr Antagonistic role of hnRNP A1 and KSRP in the regulation of Let-7a biogenesis
title_full_unstemmed Antagonistic role of hnRNP A1 and KSRP in the regulation of Let-7a biogenesis
title_short Antagonistic role of hnRNP A1 and KSRP in the regulation of Let-7a biogenesis
title_sort antagonistic role of hnrnp a1 and ksrp in the regulation of let-7a biogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2923024/
https://www.ncbi.nlm.nih.gov/pubmed/20639884
http://dx.doi.org/10.1038/nsmb.1874
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