| Literature DB >> 24910439 |
Etienne Dardenne1, Micaela Polay Espinoza1, Laurent Fattet1, Sophie Germann1, Marie-Pierre Lambert1, Helen Neil1, Eleonora Zonta1, Hussein Mortada1, Lise Gratadou1, Mathieu Deygas1, Fatima Zahra Chakrama1, Samaan Samaan1, François-Olivier Desmet1, Léon-Charles Tranchevent1, Martin Dutertre1, Ruth Rimokh1, Cyril F Bourgeois2, Didier Auboeuf3.
Abstract
The RNA helicases DDX5 and DDX17 are members of a large family of highly conserved proteins that are involved in gene-expression regulation; however, their in vivo targets and activities in biological processes such as cell differentiation, which requires reprogramming of gene-expression programs at multiple levels, are not well characterized. Here, we uncovered a mechanism by which DDX5 and DDX17 cooperate with heterogeneous nuclear ribonucleoprotein (hnRNP) H/F splicing factors to define epithelial- and myoblast-specific splicing subprograms. We then observed that downregulation of DDX5 and DDX17 protein expression during myogenesis and epithelial-to-mesenchymal transdifferentiation contributes to the switching of splicing programs during these processes. Remarkably, this downregulation is mediated by the production of miRNAs induced upon differentiation in a DDX5/DDX17-dependent manner. Since DDX5 and DDX17 also function as coregulators of master transcriptional regulators of differentiation, we propose to name these proteins "master orchestrators" of differentiation that dynamically orchestrate several layers of gene expression.Entities:
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Year: 2014 PMID: 24910439 DOI: 10.1016/j.celrep.2014.05.010
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423