Regulation of p53 activity in nuclear bodies by a specific PML isoform Journal Article


Authors: Fogal, V.; Gostissa, M.; Sandy, P.; Zacchi, P.; Sternsdorf, T.; Jensen, K.; Pandolfi, P. P.; Will, H.; Schneider, C.; Sal, G. D.
Article Title: Regulation of p53 activity in nuclear bodies by a specific PML isoform
Abstract: Covalent modification of the promyelocytic leukaemia protein (PML) by SUMO-1 is a prerequisite for the assembly of nuclear bodies (NBs), subnuclear structures disrupted in various human diseases and linked to transcriptional and growth control. Here we demonstrate that p53 is recruited into NBs by a specific PML isoform (PML3) or by coexpression of SUMO-1 and hUbc9. NB targeting depends on the direct association of p53, through its core domain, with a C-terminal region of PML3. The relocalization of p53 into NBs enhances p53 transactivation in a promoter-specific manner and affects cell survival. Our results indicate the existence of a cross-talk between PML- and p53-dependent growth suppression pathways, implying an important role for NBs and their resident proteins as modulators of p53 functions.
Keywords: oncoprotein; human cell; protein localization; cell survival; neoplasm proteins; protein binding; genetic transcription; transcription, genetic; cancer cell culture; tumor cells, cultured; protein p53; transcription factors; nuclear proteins; tumor suppressor proteins; transactivation; transcription; tumor suppressor protein p53; cellular distribution; cell nucleus; sumo-1 protein; ubiquitin-conjugating enzymes; isoprotein; protein isoforms; p53; protein modification; ubiquitins; ligases; biological transport, active; cell nucleus inclusion body; humans; human; priority journal; article; nuclear bodies; pml3; sumolation
Journal Title: EMBO Journal
Volume: 19
Issue: 22
ISSN: 0261-4189
Publisher: Wiley Blackwell  
Date Published: 2000-11-15
Start Page: 6185
End Page: 6195
Language: English
PUBMED: 11080164
PROVIDER: scopus
PMCID: PMC305840
DOI: 10.1093/emboj/19.22.6185
DOI/URL:
Notes: Export Date: 18 November 2015 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors