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  MicroRNA-9 controls dendritic development by targeting REST

Giusti, S. A., Vogl, A. M., Brockmann, M. M., Vercelli, C. A., Rein, M. L., Truembach, D., et al. (2014). MicroRNA-9 controls dendritic development by targeting REST. ELIFE, 3: UNSP e02755. doi:10.7554/eLife.02755.

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 Creators:
Giusti, Sebastian A.1, Author           
Vogl, Annette M.1, Author           
Brockmann, Marisa M.1, 2, Author           
Vercelli, Claudia A.3, Author
Rein, Martin L.2, Author
Truembach, Dietrich2, Author
Wurst, Wolfgang2, Author
Cazalla, Demian2, Author
Stein, Valentin2, Author
Deussing, Jan M.4, Author           
Refojo, Damian1, Author           
Affiliations:
1Max Planck Research Group Molecular Neurobiology (Damian Refojo), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607138              
2external, ou_persistent22              
3Department of Molecular Neurobiology, Instituto de Investigacion en Biomedicina de Buenos Aires (IBioBA)-CONICET-Partner Institute of the Max Planck Society, Buenos Aires, ou_persistent22              
4Dept. Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Max Planck Society, ou_2035294              

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 Abstract: MicroRNAs (miRNAs) are conserved noncoding RNAs that function as posttranscriptional regulators of gene expression. miR-9 is one of the most abundant miRNAs in the brain. Although the function of miR-9 has been well characterized in neural progenitors, its role in dendritic and synaptic development remains largely unknown. In order to target miR-9 in vivo, we developed a transgenic miRNA sponge mouse line allowing conditional inactivation of the miR-9 family in a spatio-temporal-controlled manner. Using this novel approach, we found that miR-9 controls dendritic growth and synaptic transmission in vivo. Furthermore, we demonstrate that miR-9-mediated downregulation of the transcriptional repressor REST is essential for proper dendritic growth.

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Language(s): eng - English
 Dates: 2014-11-18
 Publication Status: Published online
 Pages: -
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 Identifiers: ISI: 000345638500002
DOI: 10.7554/eLife.02755
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Title: ELIFE
Source Genre: Journal
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Publ. Info: elifesciences.org
Pages: - Volume / Issue: 3 Sequence Number: UNSP e02755 Start / End Page: - Identifier: ISSN: 2050-084X