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Fam83F Induces P53 Stabilisation And Promotes Its Activity
Journal
Cell Death & Differentiation
Date Issued
2019-01-28
Author(s)
Mohammed Salama
Diego Benitez-Riquelme
Seham Elabd
Ping Zhang
Matthias Glanemann
Maria Caterina Mione
Robert Goldin
Thierry Soussi
Gary Davidson
Christine Blattner
WoS ID
WOS:000485780700020
Abstract
p53 is one of the most important tumour suppressor proteins currently known. It is activated in response to DNA damage and this activation leads to proliferation arrest and cell death. The abundance and activity of p53 are tightly controlled and reductions in p53’s activity can contribute to the development of cancer. Here, we show that Fam83F increases p53 protein levels by protein stabilisation. Fam83F interacts with p53 and decreases its ubiquitination and degradation. Fam83F is induced in response to DNA damage and its overexpression also increases p53 activity in cell culture experiments and in zebrafish embryos. Downregulation of Fam83F decreases transcription of p53 target genes in response to DNA damage and increases cell proliferation, identifying Fam83F as an important regulator of the DNA damage response. Overexpression of Fam83F also enhances migration of cells harbouring mutant p53 demonstrating that it can also activate mutant forms of p53.
OCDE Subjects
Quartile (Date Issued)
Q1
License
acceso abierto