| Literature DB >> 16322758 |
Luz Tavera-Mendoza1, Tian-Tian Wang, Benjamin Lallemant, Rui Zhang, Yoshihiko Nagai, Véronique Bourdeau, Mario Ramirez-Calderon, Julie Desbarats, Sylvie Mader, John H White.
Abstract
Although 1,25-dihydroxyvitamin D3 (1,25D3) and retinoic acid (RA) have distinct developmental and physiological roles, both regulate the cell cycle. We provide molecular and genomic evidence that their cognate nuclear receptors regulate common genes through everted repeat TGA(C/T)TPyN8PuG(G/T)TCA (ER8) response elements. ER8 motifs were found in the promoters of several target genes of 1,25D3 and/or RA. Notably, an element was characterized in the cyclin-dependent kinase (CDK) inhibitor p19ink4d gene, and 1,25D3- or RA-induced p19INK4D) expression. P19ink4d knockdown together with depletion of p27kip1, another CDK inhibitor regulated by 1,25D3 and RA, rendered cells resistant to ligand-induced growth arrest. Remarkably, p19INK4D-deficient cells showed increased autophagic cell death, which was markedly enhanced by 1,25D3, but not RA, and attenuated by loss of p27KIP1. These results show a limited crosstalk between 1,25D3 and RA signalling by means of overlapping nuclear receptor DNA binding specificities, and uncover a role for p19INK4D in control of cell survival.Entities:
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Year: 2006 PMID: 16322758 PMCID: PMC1369248 DOI: 10.1038/sj.embor.7400594
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807