Translational control is required for the unfolded protein response and in vivo glucose homeostasis

Autor: Chuan Liu, Donalyn Scheuner, Thom Saunders, Susan Bonner-Weir, Benbo Song, Randal J. Kaufman, Edward L. McEwen, Patrick J. Gillespie, Ross Laybutt
Rok vydání: 2001
Předmět:
Transcriptional Activation
Protein Folding
Cell Survival
Gene Expression
Biology
Endoplasmic Reticulum
environment and public health
Islets of Langerhans
Mice
Eukaryotic translation
Translational regulation
Glucose homeostasis
Initiation factor
Animals
Homeostasis
EIF2AK3
RNA
Messenger

Phosphorylation
Molecular Biology
Endoplasmic Reticulum Chaperone BiP
Germ-Line Mutation
Heat-Shock Proteins
Endoplasmic reticulum
Homozygote
Gluconeogenesis
Cell Biology
Blood Proteins
Molecular biology
Activating Transcription Factors
Hypoglycemia
Mice
Mutant Strains

DNA-Binding Proteins
enzymes and coenzymes (carbohydrates)
Glucose
Animals
Newborn

Mutagenesis
Protein Biosynthesis
Unfolded protein response
CCAAT-Enhancer-Binding Proteins
Carrier Proteins
Transcription Factor CHOP
Molecular Chaperones
Transcription Factors
Zdroj: Molecular cell. 7(6)
ISSN: 1097-2765
Popis: The accumulation of unfolded protein in the endoplasmic reticulum (ER) attenuates protein synthesis initiation through phosphorylation of the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) at Ser51. Subsequently, transcription of genes encoding adaptive functions including the glucose-regulated proteins is induced. We show that eIF2alpha phosphorylation is required for translation attenuation, transcriptional induction, and survival in response to ER stress. Mice with a homozygous mutation at the eIF2alpha phosphorylation site (Ser51Ala) died within 18 hr after birth due to hypoglycemia associated with defective gluconeogenesis. In addition, homozygous mutant embryos and neonates displayed a deficiency in pancreatic beta cells. The results demonstrate that regulation of translation through eIF2alpha phosphorylation is essential for the ER stress response and in vivo glucose homeostasis.
Databáze: OpenAIRE