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Drosha regulates gene expression independently of RNA cleavage function.


ABSTRACT: Drosha is the main RNase III-like enzyme involved in the process of microRNA (miRNA) biogenesis in the nucleus. Using whole-genome ChIP-on-chip analysis, we demonstrate that, in addition to miRNA sequences, Drosha specifically binds promoter-proximal regions of many human genes in a transcription-dependent manner. This binding is not associated with miRNA production or RNA cleavage. Drosha knockdown in HeLa cells downregulated nascent gene transcription, resulting in a reduction of polyadenylated mRNA produced from these gene regions. Furthermore, we show that this function of Drosha is dependent on its N-terminal protein-interaction domain, which associates with the RNA-binding protein CBP80 and RNA Polymerase II. Consequently, we uncover a previously unsuspected RNA cleavage-independent function of Drosha in the regulation of human gene expression.

SUBMITTER: Gromak N 

PROVIDER: S-EPMC3898267 | biostudies-literature | 2013 Dec

REPOSITORIES: biostudies-literature

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Drosha regulates gene expression independently of RNA cleavage function.

Gromak Natalia N   Dienstbier Martin M   Macias Sara S   Plass Mireya M   Eyras Eduardo E   Cáceres Javier F JF   Proudfoot Nicholas J NJ  

Cell reports 20131219 6


Drosha is the main RNase III-like enzyme involved in the process of microRNA (miRNA) biogenesis in the nucleus. Using whole-genome ChIP-on-chip analysis, we demonstrate that, in addition to miRNA sequences, Drosha specifically binds promoter-proximal regions of many human genes in a transcription-dependent manner. This binding is not associated with miRNA production or RNA cleavage. Drosha knockdown in HeLa cells downregulated nascent gene transcription, resulting in a reduction of polyadenylate  ...[more]

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