Resistance to diverse drugs and ultraviolet light conferred by overexpression of a novel human 26 S proteasome subunit

被引:75
作者
Spataro, V
Toda, T
Craig, R
Seeger, M
Dubiel, W
Harris, AL
Norbury, C
机构
[1] UNIV OXFORD, JOHN RADCLIFFE HOSP,INST MOL MED, IMPERIAL CANC RES FUND,MOL ONCOL LAB, OXFORD OX3 9DS, ENGLAND
[2] IMPERIAL CANC RES FUND, CELL REGULAT LAB, LONDON WC2A 3PX, ENGLAND
[3] HUMBOLDT UNIV BERLIN, CHARITE, INST BIOCHEM, D-10117 BERLIN, GERMANY
关键词
D O I
10.1074/jbc.272.48.30470
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have investigated the usefulness of the fission yeast Schizosaccharomyces pombe as a model organism for the discovery of novel modes of drug resistance in human cells, In fission yeast, overexpression of the essential pad1(+) gene confers pleiotropic drug resistance through a pathway involving an AP-1 transcription factor encoded by pap1(+), We have identified POH1, a human pad1 homologue that can substitute fully for pad1(+) and induce AP-1-dependent drug resistance in fission yeast, POH1 also confers P-glycoprotein-independent resistance to taxol (paclitaxel), doxorubicin, 7-hydroxy-staurosporine, and ultraviolet Light when transiently overexpressed in mammalian cells, Poh1 is a previously unidentified component of the human 26 S proteasome, a multiprotein complex that degrades proteins targeted for destruction by the ubiquitin pathway. Hence, Poh1 is part of a conserved mechanism that determines cellular susceptibility to cytotoxic agents, perhaps by influencing the ubiquitin-dependent proteolysis of transcription factors.
引用
收藏
页码:30470 / 30475
页数:6
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