DNA damage-inducible phosphorylation of p53 at N-terminal sites including a novel site, Ser20, requires tetramerization

被引:267
作者
Shieh, SY
Taya, Y
Prives, C [1 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[2] Natl Canc Ctr, Res Inst, Chuo Ku, Tokyo 104, Japan
关键词
DNA damage; oligomerization; p53; phosphorylation;
D O I
10.1093/emboj/18.7.1815
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Upon DNA damage, p53 has been shown to be modified at a number of N-terminal phosphorylation sites including Ser15 and -33, Here we show that phosphorylation is induced as well at a novel site, Ser20, Phosphorylation at Ser15, -20 and -33 can occur within minutes of DNA damage. Interestingly, while the DNA-binding activities of p53 appear to be dispensable, efficient phosphorylation at these three sites requires the tetramerization domain of p53, Substitution of an artificial tetramerization domain for this region also permits phosphorylation at the N-terminus, suggesting that oligomerization is important for DNA damage-induced signalling to p53.
引用
收藏
页码:1815 / 1823
页数:9
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