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RNA解旋酶DDX5和DDX17在细胞分化过程中动态协调转录、微小RNA(miRNA)和剪接程序。

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

作者信息

Dardenne Etienne, Polay Espinoza Micaela, Fattet Laurent, Germann Sophie, Lambert Marie-Pierre, Neil Helen, Zonta Eleonora, Mortada Hussein, Gratadou Lise, Deygas Mathieu, Chakrama Fatima Zahra, Samaan Samaan, Desmet François-Olivier, Tranchevent Léon-Charles, Dutertre Martin, Rimokh Ruth, Bourgeois Cyril F, Auboeuf Didier

机构信息

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.

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.

出版信息

Cell Rep. 2014 Jun 26;7(6):1900-13. doi: 10.1016/j.celrep.2014.05.010. Epub 2014 Jun 6.

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.

摘要

RNA解旋酶DDX5和DDX17是一大类高度保守蛋白质家族的成员,这些蛋白质参与基因表达调控;然而,它们在体内的靶点以及在细胞分化等生物过程中的活性尚未得到充分表征,细胞分化需要在多个层面上对基因表达程序进行重编程。在这里,我们揭示了一种机制,通过该机制DDX5和DDX17与异质性核核糖核蛋白(hnRNP)H/F剪接因子合作,以定义上皮细胞和成肌细胞特异性剪接子程序。然后我们观察到,在肌生成和上皮-间充质转化过程中,DDX5和DDX17蛋白表达的下调有助于这些过程中剪接程序的转换。值得注意的是,这种下调是由分化时以DDX5/DDX17依赖方式诱导产生的miRNA介导的。由于DDX5和DDX17还作为分化的主要转录调节因子的共调节因子发挥作用,我们建议将这些蛋白质命名为分化的“主要协调者”,它们动态地协调基因表达的多个层面。

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