Fiche publication
Date publication
septembre 2017
Journal
Cell death and differentiation
Auteurs
Membres identifiés du Cancéropôle Est :
Dr DOMON-DELL Claire
,
Dr DULUC Isabelle
,
Dr FREUND Jean-Noël
,
Dr GROSS Isabelle
,
Pr REIMUND Jean-Marie
Tous les auteurs :
Balbinot C, Vanier M, Armant O, Nair A, Penichon J, Soret C, Martin E, Saandi T, Reimund JM, Deschamps J, Beck F, Domon-Dell C, Gross I, Duluc I, Freund JN
Lien Pubmed
Résumé
On the basis of phylogenetic analyses, we uncovered a variant of the CDX2 homeobox gene, a major regulator of the development and homeostasis of the gut epithelium, also involved in cancer. This variant, miniCDX2, is generated by alternative splicing coupled to alternative translation initiation, and contains the DNA-binding homeodomain but is devoid of transactivation domain. It is predominantly expressed in crypt cells, whereas the CDX2 protein is present in crypt cells but also in differentiated villous cells. Functional studies revealed a dominant-negative effect exerted by miniCDX2 on the transcriptional activity of CDX2, and conversely similar effects regarding several transcription-independent functions of CDX2. In addition, a regulatory role played by the CDX2 and miniCDX2 homeoproteins on their pre-mRNA splicing is displayed, through interactions with splicing factors. Overexpression of miniCDX2 in the duodenal Brunner glands leads to the expansion of the territory of these glands and ultimately to brunneroma. As a whole, this study characterized a new and original variant of the CDX2 homeobox gene. The production of this variant represents not only a novel level of regulation of this gene, but also a novel way to fine-tune its biological activity through the versatile functions exerted by the truncated variant compared to the full-length homeoprotein. This study highlights the relevance of generating protein diversity through alternative splicing in the gut and its diseases.Cell Death and Differentiation advance online publication, 1 September 2017; doi:10.1038/cdd.2017.140.
Mots clés
Alternative Splicing, Animals, CDX2 Transcription Factor, genetics, Caco-2 Cells, Cecum, metabolism, Cell Differentiation, genetics, Genes, Homeobox, HCT116 Cells, HEK293 Cells, Humans, Intestinal Mucosa, metabolism, Mice, Mice, Transgenic, RNA Precursors, genetics, Transfection
Référence
Cell Death Differ.. 2017 Sep;:
