Journal
NUCLEIC ACIDS RESEARCH
Volume 38, Issue 3, Pages 764-777Publisher
OXFORD UNIV PRESS
DOI: 10.1093/nar/gkp1034
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Funding
- National Taiwan University [97R0333]
- National Science Council [NSC96-2321-B002-008, NSC97-2320-B182-027-MY3]
- Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan
- Chang Gung Memorial Hospital
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Cells respond to environmental stress by inducing translation of a subset of mRNAs important for survival or apoptosis. CHOP, a downstream transcriptional target of stress-induced ATF4, is also regulated translationally in a uORF-dependent manner under stress. Low concentration of anisomycin induces CHOP expression at both transcriptional and translational levels. To study specifically the translational aspect of CHOP expression, and further clarify the regulatory mechanisms underlying stress-induced translation initiation, we developed a CMV promoter-regulated, uORF(chop)-driven reporter platform. Here we show that anisomycin-induced CHOP expression depends on phosphorylated eIF4E/S209 and eIF2 alpha/S51. Contrary to phospho-eIF2 alpha/S51, phospho-eIF4E/S209 is not involved in thapsigargin-induced CHOP expression. Studies using various kinase inhibitors and mutants uncovered that both the p38MAPK-Mnk and mTOR signaling pathways contribute to stress-responsive reporter and CHOP expression. We also demonstrated that anisomycin-induced translation is tightly regulated by partner binding preference of eIF4E. Furthermore, mutating the uORF sequence abolished the anisomycin-induced association of chop mRNA with phospho-eIF4E and polysomes, thus demonstrating the significance of this cis-regulatory element in conferring on the transcript a stress-responsive translational inducibility. Strikingly, although insulin treatment activated ERK-Mnk and mTOR pathways, and consequently eIF4E/S209 phosphorylation, it failed to induce phospho-eIF2 alpha/S51 and reporter translation, thus pinpointing a crucial determinant in stress-responsive translation.
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