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PMID: 7709427 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Review

Regulation of protein synthesis by heme-regulated eIF-2 alpha kinase.

Trends in biochemical sciences ·Vol. 20 ·No. 3 ·1995-03-00 ·Pages 105-8

Chen JJ, London IM

Abstract

Protein synthesis is regulated by the phosphorylation of the alpha-subunit of eukaryotic initiation factor 2 (eIF-2 alpha) in a variety of cells. At present, there are two distinct mammalian eIF-2 alpha kinases that have been cloned, the double-stranded-RNA-dependent eIF-2 alpha kinase (PKR) and the heme-regulated eIF-2 alpha kinase (HRI). HRI is activated under conditions of heme deficiency in immature erythroid cells, and its activity is inhibited by heme. The high levels of HRI in reticulocytes indicate that its major physiological role is the regulation of protein synthesis, particularly of hemoglobin, according to the concentration of heme in these cells.

MeSH Terms
Animals Heat-Shock Proteins/metabolism Heme/metabolism Humans Protein Biosynthesis Protein Conformation Protein Serine-Threonine Kinases/chemistry,metabolism eIF-2 Kinase
Chemicals
Heat-Shock Proteins Heme Protein Serine-Threonine Kinases eIF-2 Kinase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Chen J J
Massachusetts Institute of Technology, Harvard-MIT Division of Health Sciences and Technology, Cambridge 02139, USA.
London I M
Article Info
Journal
Trends in biochemical sciences
Abbr.
Trends Biochem Sci
ISSN
0968-0004
Published
1995-03-00
Pages
105-8
Language
English
Region
England
NLM ID
7610674
Subset
IM
Grants
NIDDK NIH HHS · R01 DK016272 · United States
NIDDK NIH HHS · DK-16272 · United States
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