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RNA helicases DDX5 and DDX17 dynamically orchestrate transcription, miRNA, and splicing programs in cell differentiation. | LitMetric

RNA helicases DDX5 and DDX17 dynamically orchestrate transcription, miRNA, and splicing programs in cell differentiation.

Cell Rep

INSERM U1052, Centre de Recherche en Cancérologie de Lyon, 69008 Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, 69008 Lyon, France; Université Claude Bernard Lyon 1, 69008 Lyon, France; Centre Léon Bérard, 69008 Lyon, France. Electronic address:

Published: June 2014

AI Article Synopsis

  • DDX5 and DDX17 are important RNA helicases that play a role in regulating gene expression and are involved in processes like cell differentiation, but their specific functions in vivo are not fully understood.
  • This study reveals that DDX5 and DDX17 work with splicing factors to create specific splicing programs unique to epithelial and myoblast cells.
  • The downregulation of these proteins during differentiation is influenced by miRNAs and is crucial for transitioning splicing programs, leading to the proposal of calling them "master orchestrators" of differentiation.

Article 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.

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Source
http://dx.doi.org/10.1016/j.celrep.2014.05.010DOI Listing

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