After a decade of study-ING, a PHD for a versatile family of proteins

被引:124
作者
Soliman, Mohamed A.
Riabowol, Karl
机构
[1] Univ Calgary, Dept Biochem & Mol Biol, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Dept Oncol, Calgary, AB T2N 4N1, Canada
基金
加拿大健康研究院;
关键词
CANDIDATE TUMOR-SUPPRESSOR; NUCLEOTIDE EXCISION-REPAIR; PLANT HOMEODOMAIN FINGER; HISTONE H3; CELL-PROLIFERATION; LYSINE-4; METHYLATION; BINDING; P53; P33(ING1); GROWTH;
D O I
10.1016/j.tibs.2007.08.006
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
The INhibitor of Growth (ING) family of type II tumour suppressors are encoded by five genes in mammals (ING1-ING5), most of which encode multiple isoforms via splicing, and all of which contain a highly conserved plant homeodomain (PHD) finger motif. Since their discovery approximately ten years ago, significant progress has been made in understanding their subcellular targeting, their relationship to p53, their activation by bioactive phospholipids, and their key role in reading the histone code via PHD fingers, with subsequent effects on histone acetylation and transcriptional regulation. In the past year, we have begun to understand how ING proteins integrate stress signals with interpretation and modification of the histone epigenetic code to function as tumour suppressors.
引用
收藏
页码:509 / 519
页数:11
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