DGCR8 acts as an adaptor for the exosome complex to degrade double-stranded structured RNAs

Sara Macias Ribela, Ross Cordiner, Phillipe Gautier, Mireya Plass, Javier F. Cáceres

Research output: Contribution to journalArticlepeer-review

Abstract

The Microprocessor complex (DGCR8/Drosha) is required for microRNA (miRNA) biogenesis but also binds and regulates the stability of several types of cellular RNAs. Of particular interest, DGCR8 controls the stability of mature small nucleolar RNA (snoRNA) transcripts independently of Drosha, suggesting the existence of alternative DGCR8 complex(es) with other nucleases to process a variety of cellular RNAs. Here, we found that DGCR8 copurifies with subunits of the nuclear exosome, preferentially associating with its hRRP6-containing nucleolar form. Importantly, we demonstrate that DGCR8 is essential for the recruitment of the exosome to snoRNAs and to human telomerase RNA. In addition, we show that the DGCR8/exosome complex controls the stability of the human telomerase RNA component (hTR/TERC). Altogether, these data suggest that DGCR8 acts as an adaptor to recruit the exosome complex to structured RNAs and induce their degradation.
Original languageEnglish
Pages (from-to)873-885
Number of pages13
JournalMolecular Cell
Volume60
Issue number6
Early online date10 Dec 2015
DOIs
Publication statusPublished - 17 Dec 2015

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