Global analysis of RNA-binding sites of CUGBP1 and MBNL1 reveals their preferential binding to 3’ UTRs and a new role for MBNL1 in mRNA decay

Akio Masuda, Henriette Skovgaard Andersen, Thomas Doktor, T Okamoto, M Ito, Brage Storstein Andresen, Kinji Ohno

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Abstrakt

CUGBP1 and MBNL1 are developmentally regulated RNA-binding proteins that are causally associated with myotonic dystrophy type 1. We globally determined the in vivo RNA-binding sites of CUGBP1 and MBNL1. Interestingly, CUGBP1 and MBNL1 are both preferentially bound to 39 UTRs. Analysis of CUGBP1- and MBNL1-bound 3' UTRs demonstrated that both factors mediate accelerated mRNA decay and temporal profiles of expression arrays supported this. Role of CUGBP1 on accelerated mRNA decay has been previously reported, but the similar function of MBNL1 has not been reported to date. It is well established that CUGBP1 and MBNL1 regulate alternative splicing. Screening by exon array and validation by RT-PCR revealed position dependence of CUGBP1- and MBNL1-binding sites on the resulting alternative splicing pattern. This study suggests that regulation of CUGBP1 and MBNL1 is essential for accurate control of destabilization of a broad spectrum of mRNAs as well as of alternative splicing events.
OriginalsprogEngelsk
TidsskriftScientific Reports
Vol/bind2
Udgave nummer209
ISSN2045-2322
DOI
StatusUdgivet - 2012

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