Protein synthesis upon acute nutrient restriction relies on proteasome function

被引:278
作者
Vabulas, RM [1 ]
Hartl, FU [1 ]
机构
[1] Max Planck Inst Biochem, Dept Cellular Biochem, D-82152 Martinsried, Germany
关键词
D O I
10.1126/science.1121925
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mechanisms that protect mammalian cells against amino acid deprivation are only partially understood. We found that during an acute decrease. in external amino acid supply, before up-regulation of the autophagosomal-lysosomai pathway, efficient translation was ensured by proteasomal protein degradation. Amino acids for the synthesis of new proteins were supplied by the degradation of preexisting proteins, whereas nascent and newly formed polypeptides remained largely protected from proteolysis. Proteasome inhibition during nutrient deprivation caused rapid amino acid depletion and marked impairment of translation. Thus, the proteasome plays a crucial rote in cell survival after acute disruption of amino acid supply.
引用
收藏
页码:1960 / 1963
页数:4
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