Control of mRNA decay by heat shock ubiquitin proteasome pathway

被引:344
作者
Laroia, G
Cuesta, R
Brewer, G
Schneider, RJ [1 ]
机构
[1] NYU, Sch Med, Dept Microbiol & Biochem, New York, NY 10016 USA
[2] Wake Forest Univ, Sch Med, Dept Microbiol & Immunol, Winston Salem, NC 27157 USA
关键词
D O I
10.1126/science.284.5413.499
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
Cytokine and proto-oncogene messenger RNAs (mRNAs) are rapidly degraded through AU-rich elements in the 3' untranslated region. Rapid decay involves AU-rich binding protein AUF1, which complexes with heat shock proteins hsc70-hsp70, translation initiation factor elF4G, and poly(A) binding protein. AU-rich mRNA decay is associated with displacement of elF4G from AUF1, ubiquitination of AUF1, and 'degradation of AUF1 by proteasomes. Induction of hsp70 by heat shock, down-regulation of the ubiquitin-proteasome network, or inactivation of ubiquitinating enzyme E1 all result in hsp70 sequestration of AUF1 in the perinucleus-nucleus, and all three processes block decay of AU-rich mRNAs and AUF1 protein. These results link the rapid degradation of cytokine mRNAs to the ubiquitin-proteasome pathway.
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页码:499 / 502
页数:4
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