eIF-2 kinases: regulators of general and gene-specific translation initiation
- PMID: 7855893
- DOI: 10.1016/0968-0004(94)90136-8
eIF-2 kinases: regulators of general and gene-specific translation initiation
Abstract
Phosphorylation of eukaryotic initiation factor-2 (eIF-2) is an important mechanism regulating general translation initiation. Two mammalian eIF-2 kinases, the double-stranded-RNA-dependent kinase (PKR) and heme-regulated inhibitor kinase (HRI), have been characterized by sequencing, revealing shared sequence and structural features distinct from other eukaryotic protein kinases. Recent work in yeast has shown that a third related kinase, GCN2, also phosphorylates the regulated site in eIF-2. However, unlike the mammalian kinases, this kinase regulates gene-specific translation. Current models are presented for the regulation of each eIF-2 kinase, and the molecular basis for how this general form of regulation is adapted to control expression of a single species of messenger RNA is discussed.
Similar articles
-
Mammalian eukaryotic initiation factor 2 alpha kinases functionally substitute for GCN2 protein kinase in the GCN4 translational control mechanism of yeast.Proc Natl Acad Sci U S A. 1993 May 15;90(10):4616-20. doi: 10.1073/pnas.90.10.4616. Proc Natl Acad Sci U S A. 1993. PMID: 8099443 Free PMC article.
-
Cloning of the cDNA of the heme-regulated eukaryotic initiation factor 2 alpha (eIF-2 alpha) kinase of rabbit reticulocytes: homology to yeast GCN2 protein kinase and human double-stranded-RNA-dependent eIF-2 alpha kinase.Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7729-33. doi: 10.1073/pnas.88.17.7729. Proc Natl Acad Sci U S A. 1991. PMID: 1679235 Free PMC article.
-
The eIF-2alpha kinases and the control of protein synthesis.FASEB J. 1996 Oct;10(12):1378-87. doi: 10.1096/fasebj.10.12.8903508. FASEB J. 1996. PMID: 8903508 Review.
-
A mammalian homologue of GCN2 protein kinase important for translational control by phosphorylation of eukaryotic initiation factor-2alpha.Genetics. 2000 Feb;154(2):787-801. doi: 10.1093/genetics/154.2.787. Genetics. 2000. PMID: 10655230 Free PMC article.
-
Regulation of protein synthesis by heme-regulated eIF-2 alpha kinase.Trends Biochem Sci. 1995 Mar;20(3):105-8. doi: 10.1016/s0968-0004(00)88975-6. Trends Biochem Sci. 1995. PMID: 7709427 Review.
Cited by
-
The Role of PKR as a Potential Target for Treating Cardiovascular Diseases.Curr Cardiol Rev. 2017;13(1):28-31. doi: 10.2174/1573403x12666160526122600. Curr Cardiol Rev. 2017. PMID: 27225893 Free PMC article. Review.
-
Post-transcriptional control of type I interferon induction by porcine reproductive and respiratory syndrome virus in its natural host cells.Viruses. 2012 May;4(5):725-33. doi: 10.3390/v4050725. Epub 2012 May 2. Viruses. 2012. PMID: 22754646 Free PMC article. Review.
-
Paramyxovirus-induced shutoff of host and viral protein synthesis: role of the P and V proteins in limiting PKR activation.J Virol. 2008 Jan;82(2):828-39. doi: 10.1128/JVI.02023-07. Epub 2007 Oct 31. J Virol. 2008. PMID: 17977969 Free PMC article.
-
Genetic evidence for functional specificity of the yeast GCN2 kinase.Mol Gen Genet. 1996 Jul 19;251(5):613-8. doi: 10.1007/BF02173652. Mol Gen Genet. 1996. PMID: 8709969
-
Hsp90 binds and regulates Gcn2, the ligand-inducible kinase of the alpha subunit of eukaryotic translation initiation factor 2 [corrected].Mol Cell Biol. 1999 Dec;19(12):8422-32. doi: 10.1128/MCB.19.12.8422. Mol Cell Biol. 1999. PMID: 10567567 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases