Phosphoproteins in Stress-Induced Disease

被引:36
作者
Dalton, Lucy E. [1 ]
Healey, Eleanor [1 ]
Irving, James [1 ]
Marciniak, Stefan J. [1 ]
机构
[1] Univ Cambridge, Dept Med, Div Resp Med, Cantbridge Inst Med Res, Cambridge CB2 2QQ, England
来源
PROTEIN PHOSPHORYLATION IN HEALTH AND DISEASE | 2012年 / 106卷
关键词
DOUBLE-STRANDED-RNA; ENDOPLASMIC-RETICULUM STRESS; ACTIVATED PROTEIN-KINASE; REGULATED EIF2-ALPHA KINASE; GLUCAGON-LIKE PEPTIDE-1; OPEN READING FRAMES; GCN4; MESSENGER-RNA; UNCHARGED TRANSFER-RNA; AMINO-ACID DEFICIENCY; BETA-CELL DYSFUNCTION;
D O I
10.1016/B978-0-12-396456-4.00003-1
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 integrated stress response (ISR) is an evolutionarily conserved homeostatic program activated by specific pathological states. These include amino acid deprivation, viral infection, iron deficiency, and the misfolding of proteins within the endoplasmic reticulum (ER), the so-called ER stress. Although apparently disparate, each of these stresses induces phosphorylation of a translation initiation factor, eIF2 alpha, to attenuate new protein translation while simultaneously triggering a transcriptional program. This is achieved by four homologous stress-sensing kinases: GCN2, PKR, HRI, and PERK. In addition to these kinases, mammals possess two specific eIF2 alpha phosphatases, GADD34 and CReP, which play crucial roles in the recovery of protein synthesis following the initial insult. They are not only important in embryonic development but also appear to play important roles in disease, particularly cancer. In this chapter, we discuss each of the eIF2 alpha kinases, in turn, with particular emphasis on their regulation and the new insights provided by recent structural studies. We also discuss the potential for developing novel drug therapies that target the ISR.
引用
收藏
页码:189 / 221
页数:33
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