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Proc Natl Acad Sci U S A. 2012 Feb 28;109(9):3347-52. doi: 10.1073/pnas.1112427109. Epub 2012 Feb 9.

TDP-43 promotes microRNA biogenesis as a component of the Drosha and Dicer complexes.

Author information

1
Laboratory of RNA Function, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan. ykawahara@rna.med.osaka-u.ac.jp

Abstract

Although aberrant microRNA (miRNA) expression is linked to human diseases including cancer, the mechanisms that regulate the expression of each individual miRNA remain largely unknown. TAR DNA-binding protein-43 (TDP-43) is homologous to the heterogeneous nuclear ribonucleoproteins (hnRNPs), which are involved in RNA processing, and its abnormal cellular distribution is a key feature of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD), two neurodegenerative diseases. Here, we show that TDP-43 facilitates the production of a subset of precursor miRNAs (pre-miRNAs) by both interacting with the nuclear Drosha complex and binding directly to the relevant primary miRNAs (pri-miRNAs). Furthermore, cytoplasmic TDP-43, which interacts with the Dicer complex, promotes the processing of some of these pre-miRNAs via binding to their terminal loops. Finally, we show that involvement of TDP-43 in miRNA biogenesis is indispensable for neuronal outgrowth. These results support a previously uncharacterized role for TDP-43 in posttranscriptional regulation of miRNA expression in both the nucleus and the cytoplasm.

PMID:
22323604
PMCID:
PMC3295278
DOI:
10.1073/pnas.1112427109
[Indexed for MEDLINE]
Free PMC Article
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