Crm1 (Xpol) dependent nuclear export of the budding yeast transcription factor yAP-1 is sensitive to oxidative stress

被引:134
作者
Kuge, S
Toda, T
Iizuka, N
Nomoto, A
机构
[1] Univ Tokyo, Inst Med Sci, Dept Microbiol, Minato Ku, Tokyo 1088639, Japan
[2] Imperial Canc Res Fund, Lab Cell Regulat, London WC2A 3PX, England
[3] Nagoya City Univ, Sch Med, Dept Virol, Nagoya, Aichi 4678601, Japan
关键词
D O I
10.1046/j.1365-2443.1998.00209.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: The yAP-1 transcription factor is crucial for the oxidative stress response of the budding yeast Saccharomyces cerevisiae; its activity is induced in response to oxidative stress, and as a consequence the expression of a number of target genes is enhanced. We have shown previously that yAP-1 is mainly found in the cytoplasm, but that upon the imposition of oxidative stress it localizes to the nucleus. In this study, we addressed the mechanism through which yAP-1 nuclear localization is regulated. Results: Here we show that yAP-1 localization is mediated by active export from the nucleus, resulting from the activity of Crm1 (XpoI), a conserved protein that functions as an export receptor which recognizes the nuclear export signal (NES). When Crm1 expression was repressed, yAP-1 was localized in the nucleus and induced the expression of a yAP-1 dependent target gene. Our results also suggest that the cysteine rich domain (CRD), at the C-terminus of yAP-1, functions as an export recognition sequence, yAP-1 and Crm1 interact in vivo and this interaction is reduced in response to oxidative stress. Conclusions: These results suggest a novel regulatory mechanism of nucleocytoplasmic transport which is dependent upon a redox sensitive nuclear export pathway.
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页码:521 / 532
页数:12
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