Neurotrophins are growth factors that are important in neuronal development and survival as well as synapse formation and plasticity. Many of the effects of neurotrophins are mediated by changes in protein expression as a result of altered transcription or translation. To determine whether neurotrophins regulate the production of microRNAs (miRNAs), small RNA species that modulate protein translation or mRNA stability, we used deep sequencing to identify BDNF (brain-derived neurotrophic factor)-induced miRNAs in cultured primary cortical mouse neurons. This revealed that the miR-212/132 cluster contained the miRNAs most responsive to BDNF treatment. This cluster was found to produce four miRNAs: miR-132, miR-132*, miR-212 and miR-212*. Using specific inhibitors, mouse models and promoter analysis we have shown that the regulation of the transcription of the miR-212/132 miRNA cluster and the miRNAs derived from it are regulated by the ERK1/2 (extracellular-signalregulated kinase 1/2) pathway, via both MSK (mitogen and stress-activated kinase)-dependent and -independent mechanisms.
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Research Article|
May 13 2010
Regulation of the miR-212/132 locus by MSK1 and CREB in response to neurotrophins
Judit Remenyi;
Judit Remenyi
1
*Wellcome Trust Centre for Gene Regulation and Expression, College of Life Sciences, Sir James Black Complex, University of Dundee, Dundee DD1 5EH, Scotland, U.K.
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Christopher J. Hunter;
Christopher J. Hunter
1
†MRC Protein Phosphorylation Unit, College of Life Sciences, Sir James Black Complex, University of Dundee, Dundee DD1 5EH, Scotland, U.K.
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Christian Cole;
Christian Cole
‡College of Life Sciences, University of Dundee, Dundee DD1 5EH, Scotland, U.K.
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Hideaki Ando;
Hideaki Ando
2
§Oregon Stem Cell Centre, Oregon Health & Science University, Portland, OR 97239-3098, U.S.A.
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Soren Impey;
Soren Impey
§Oregon Stem Cell Centre, Oregon Health & Science University, Portland, OR 97239-3098, U.S.A.
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Claire E. Monk;
Claire E. Monk
†MRC Protein Phosphorylation Unit, College of Life Sciences, Sir James Black Complex, University of Dundee, Dundee DD1 5EH, Scotland, U.K.
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Kirsty J. Martin;
Kirsty J. Martin
†MRC Protein Phosphorylation Unit, College of Life Sciences, Sir James Black Complex, University of Dundee, Dundee DD1 5EH, Scotland, U.K.
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Geoffrey J. Barton;
Geoffrey J. Barton
‡College of Life Sciences, University of Dundee, Dundee DD1 5EH, Scotland, U.K.
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Gyorgy Hutvagner;
Gyorgy Hutvagner
3
*Wellcome Trust Centre for Gene Regulation and Expression, College of Life Sciences, Sir James Black Complex, University of Dundee, Dundee DD1 5EH, Scotland, U.K.
3Correspondence may be addressed to either of these authors (email [email protected] or [email protected]).
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J. Simon C. Arthur
J. Simon C. Arthur
3
†MRC Protein Phosphorylation Unit, College of Life Sciences, Sir James Black Complex, University of Dundee, Dundee DD1 5EH, Scotland, U.K.
3Correspondence may be addressed to either of these authors (email [email protected] or [email protected]).
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Publisher: Portland Press Ltd
Received:
January 04 2010
Revision Received:
March 22 2010
Accepted:
March 23 2010
Accepted Manuscript online:
March 23 2010
Online ISSN: 1470-8728
Print ISSN: 0264-6021
© The Authors Journal compilation © 2010 Biochemical Society
2010
Biochem J (2010) 428 (2): 281–291.
Article history
Received:
January 04 2010
Revision Received:
March 22 2010
Accepted:
March 23 2010
Accepted Manuscript online:
March 23 2010
Citation
Judit Remenyi, Christopher J. Hunter, Christian Cole, Hideaki Ando, Soren Impey, Claire E. Monk, Kirsty J. Martin, Geoffrey J. Barton, Gyorgy Hutvagner, J. Simon C. Arthur; Regulation of the miR-212/132 locus by MSK1 and CREB in response to neurotrophins. Biochem J 1 June 2010; 428 (2): 281–291. doi: https://doi.org/10.1042/BJ20100024
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