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Regulation of microRNA-mediated gene silencing by microRNA precursors.


ABSTRACT: Processing of microRNAs (miRNAs) from their precursors to their biologically active mature forms is regulated during development and cancer. We show that mouse pri- or pre-miR-151 can bind to and compete with mature miR-151-5p and miR-151-3p for binding sites contained within the complementary regions of the E2f6 mRNA 3' untranslated region (UTR). E2f6 mRNA levels were directly regulated by pri- or pre-miR-151. Conversely, miR-151-mediated repression of ARHGDIA mRNA was dependent on the level of mature miR-151 because only the mature miRNA binds the 3' UTR. Thus, processing of miR-151 can have different effects on separate mRNA targets within a cell. A bioinformatics pipeline revealed additional candidate regions where precursor miRNAs can compete with their mature miRNA counterparts. We validated this experimentally for miR-124 and the SNAI2 3' UTR. Hence, miRNA precursors can serve as post-transcriptional regulators of miRNA activity and are not mere biogenesis intermediates.

SUBMITTER: Roy-Chaudhuri B 

PROVIDER: S-EPMC4244528 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature

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Regulation of microRNA-mediated gene silencing by microRNA precursors.

Roy-Chaudhuri Biswajoy B   Valdmanis Paul N PN   Zhang Yue Y   Wang Qing Q   Luo Qing-Jun QJ   Kay Mark A MA  

Nature structural & molecular biology 20140803 9


Processing of microRNAs (miRNAs) from their precursors to their biologically active mature forms is regulated during development and cancer. We show that mouse pri- or pre-miR-151 can bind to and compete with mature miR-151-5p and miR-151-3p for binding sites contained within the complementary regions of the E2f6 mRNA 3' untranslated region (UTR). E2f6 mRNA levels were directly regulated by pri- or pre-miR-151. Conversely, miR-151-mediated repression of ARHGDIA mRNA was dependent on the level of  ...[more]

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