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Nucleic Acids Res. 2009 Oct;37(18):6092-104. doi: 10.1093/nar/gkp674. Epub 2009 Aug 21.

Identification and functional characterization of two new transcriptional variants of the human p63 gene.

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1
Dipartimento di Biochimica e Biologia Molecolare E. Quagliariello, Università degli Studi di Bari, via Orabona 4, 70126 Bari, Italy.

Abstract

p63 belongs to a family of transcription factors, which, while demonstrating striking conservation of functional domains, regulate distinct biological functions. Its principal role is in the regulation of epithelial commitment, differentiation and maintenance programs, during embryogenesis and in adult tissues. The p63 gene has a complex transcriptional pattern, producing two subclasses of N-terminal isoforms (TA and DeltaN) which are alternatively spliced at the C-terminus. Here, we report the identification of two new C-terminus p63 variants, we named p63 delta and epsilon, that increase from 6 to 10 the number of the p63 isoforms. Expression analysis of all p63 variants demonstrates a tissue/cell-type-specific nature of p63 alternative transcript expression, probably related to their different cellular functions. We demonstrate that the new p63 variants as DeltaN isoforms are active as transcription factors as they have nuclear localization and can modulate the expression of p63 target genes. Moreover, we report that, like DeltaNp63alpha, DeltaNp63delta and epsilon sustain cellular proliferation and that their expression decreases during keratinocyte differentiation, suggesting their involvement in this process. Taken together, our results demonstrate the existence of novel p63 proteins whose expression should be considered in future studies on the roles of p63 in the regulation of cellular functions.

PMID:
19700772
PMCID:
PMC2764424
DOI:
10.1093/nar/gkp674
[Indexed for MEDLINE]
Free PMC Article
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