Emerging common themes in regulation of PIKKs and PI3Ks

被引:227
作者
Lempiaeinen, Harri [1 ]
Halazonetis, Thanos D. [1 ,2 ]
机构
[1] Univ Geneva, Dept Mol Biol, CH-1211 Geneva 4, Switzerland
[2] Univ Geneva, Dept Biochem, CH-1211 Geneva 4, Switzerland
关键词
ATM; ATR; DNA-PK; PIKK; PI3K; CANCER-SPECIFIC MUTATIONS; MAMMARY EPITHELIAL-CELLS; MESSENGER-RNA DECAY; PHOSPHOINOSITIDE; 3-KINASE; MAMMALIAN TARGET; ATAXIA-TELANGIECTASIA; CATALYTIC SUBUNIT; DNA-DAMAGE; FKBP12-RAPAMYCIN-ASSOCIATED PROTEIN; PHOSPHATIDYLINOSITOL 3'-KINASE;
D O I
10.1038/emboj.2009.281
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
Phosphatidylinositol-3 kinase-related kinases (PIKKs) comprise a family of protein kinases that respond to various stresses, including DNA damage, blocks in DNA replication, availability of nutrients and errors in mRNA splicing. PIKKs are characterized by the presence of a conserved kinase domain (KD), whose activity is regulated by two C-terminal regions, referred to as PIKK-regulatory domain (PRD) and FRAP-ATM-TRRAP-C-terminal (FATC), respectively. Here, we review functional and structural data that implicate the PRD and FATC domains in regulation of PIKK activity, drawing parallels to phosphatidylinositol- 3 kinases (PI3K), lipid kinases that have sequence similarity to PIKKs. The PI3K C-terminus, which we propose to be equivalent to the PRD and FATC domains of PIKKs, is in close proximity to the activation loop of the KD, suggesting that in PIKKs, the PRD and FATC domains may regulate kinase activity by targeting the activation loop. The EMBO Journal (2009) 28, 3067-3073. doi:10.1038/emboj.2009.281; Published online 24 September 2009
引用
收藏
页码:3067 / 3073
页数:7
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