TY - JOUR
T1 - The double-stranded RNA-activated protein kinase PKR is dispensable for regulation of translation initiation in response to either calcium mobilization from the endoplasmic reticulum or essential amino acid starvation
AU - Kimball, Scot R.
AU - Clemens, Michael J.
AU - Tilleray, Vivienne J.
AU - Wek, Ronald C.
AU - Horetsky, Rick L.
AU - Jefferson, Leonard S.
N1 - Funding Information:
The authors are grateful to Joan McGwire for technical help. We also thank Dr. C. Weissmann for the mouse embryo fibroblasts and Drs. D. J. DeGracia, G. S. Krause, and R. Panniers for eIF2α antibodies. This work was supported by National Institute of Health Grants DK-13499 (L.S.J.), DK-15658 (L.S.J.), and GM49164 (R.C.W.), by American Cancer Society Grant RPG MBC-87806 (R.C.W.), and by funding from the Welcome Trust (Grant 056778) (M.J.C.), the Leukemia Research Fund (M.J.C.), and the Cancer Prevention Research Trust (M.J.C.).
PY - 2001
Y1 - 2001
N2 - The α-subunit of eukaryotic initiation factor eIF2 is a preferred substrate for the double-stranded RNA-activated protein kinase, PKR. Phosphorylation of eIF2α converts the factor from a substrate into a competitive inhibitor of the guanine nucleotide exchange factor, eIF2B, leading to a decline in mRNA translation. Early studies provided evidence implicating PKR as the kinase that phosphorylates eIF2α under conditions of cell stress such as the accumulation of misfolded proteins in the lumen of the endoplasmic reticulum, i.e., the unfolded protein response (UPR). However, the recent identification of a trans-microsomal membrane eIF2α kinase, termed PEK or PERK, suggests that this kinase, and not PKR, might be the kinase that is activated by misfolded protein accumulation. Similarly, genetic studies in yeast provide compelling evidence that a kinase termed GCN2 phosphorylates eIF2α in response to amino acid deprivation. However, no direct evidence showing activation of the mammalian homologue of GCN2 by amino acid deprivation has been reported. In the present study, we find that in fibroblasts treated with agents that promote the UPR, protein synthesis is inhibited as a result of a decrease in eIF2B activity. Furthermore, the reduction in eIF2B activity is associated with enhanced phosphorylation of eIF2α. Importantly, the magnitude of the change in each parameter is identical in wildtype cells and in fibroblasts containing a chromosomal deletion in the PKR gene (PKR-KO cells). In a similar manner, we find that during amino acid deprivation the inhibition of protein synthesis and extent of increase in eIF2α phosphorylation are identical in wildtype and PKR-KO cells. Overall, the results show that PKR is not required for increased eIF2α phosphorylation or inhibition of protein synthesis under conditions promoting the UPR or in response to amino acid deprivation.
AB - The α-subunit of eukaryotic initiation factor eIF2 is a preferred substrate for the double-stranded RNA-activated protein kinase, PKR. Phosphorylation of eIF2α converts the factor from a substrate into a competitive inhibitor of the guanine nucleotide exchange factor, eIF2B, leading to a decline in mRNA translation. Early studies provided evidence implicating PKR as the kinase that phosphorylates eIF2α under conditions of cell stress such as the accumulation of misfolded proteins in the lumen of the endoplasmic reticulum, i.e., the unfolded protein response (UPR). However, the recent identification of a trans-microsomal membrane eIF2α kinase, termed PEK or PERK, suggests that this kinase, and not PKR, might be the kinase that is activated by misfolded protein accumulation. Similarly, genetic studies in yeast provide compelling evidence that a kinase termed GCN2 phosphorylates eIF2α in response to amino acid deprivation. However, no direct evidence showing activation of the mammalian homologue of GCN2 by amino acid deprivation has been reported. In the present study, we find that in fibroblasts treated with agents that promote the UPR, protein synthesis is inhibited as a result of a decrease in eIF2B activity. Furthermore, the reduction in eIF2B activity is associated with enhanced phosphorylation of eIF2α. Importantly, the magnitude of the change in each parameter is identical in wildtype cells and in fibroblasts containing a chromosomal deletion in the PKR gene (PKR-KO cells). In a similar manner, we find that during amino acid deprivation the inhibition of protein synthesis and extent of increase in eIF2α phosphorylation are identical in wildtype and PKR-KO cells. Overall, the results show that PKR is not required for increased eIF2α phosphorylation or inhibition of protein synthesis under conditions promoting the UPR or in response to amino acid deprivation.
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U2 - 10.1006/bbrc.2000.4103
DO - 10.1006/bbrc.2000.4103
M3 - Article
C2 - 11162513
AN - SCOPUS:0034805883
SN - 0006-291X
VL - 280
SP - 293
EP - 300
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -