Activation of GCN2 in UV-irradiated cells inhibits translation

被引:253
作者
Deng, J
Harding, HP
Raught, B
Gingras, AC
Berlanga, JJ
Scheuner, D
Kaufman, RJ
Ron, D
Sonenberg, N
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, McGill Canc Ctr, Montreal, PQ H3G 1Y6, Canada
[3] NYU, Sch Med, Dept Med, Skirball Inst, New York, NY 10016 USA
[4] NYU, Sch Med, Dept Cell Biol, Skirball Inst, New York, NY 10016 USA
[5] NYU, Sch Med, Kaplan Canc Ctr, Skirball Inst, New York, NY 10016 USA
[6] Univ Michigan, Howard Hughes Med Inst, Med Ctr, Ann Arbor, MI 48109 USA
关键词
D O I
10.1016/S0960-9822(02)01037-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Background: Mammalian cells subjected to ultraviolet (UV) irradiation actively repress DNA replication, transcription, and mRNA translation. While the effects of UV irradiation on DNA replication and transcription have been extensively studied, the mechanism(s) responsible for translational repression are poorly understood. Results: Here, we demonstrate that UV irradiation elicits phosphorylation of the alpha subunit of eukaryotic translation initiation factor 2 (eIF2alpha) by activating the kinase GCN2 in a manner that does not require SAPK/JNK or p38 MAP kinase. GCN2-/- cells, and cells expressing nonphosphorylatable eIF2alpha as their only source of eIF2alpha protein, fail to repress translation in response to UV irradiation. Conclusions: These results provide a mechanism for translation inhibition by UV irradiation and identify a hitherto unrecognized role for mammalian GCN2 as a mediator of the cellular response to UV stress.
引用
收藏
页码:1279 / 1286
页数:8
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