生物
转录因子
酿酒酵母
磷酸化
DNA足迹
抄写(语言学)
细胞生物学
信号转导
脚印
生物化学
调节器
转录调控
分子生物学
DNA结合蛋白
酵母
基因
语言学
哲学
作者
Angelika Kren,Yasmine M. Mamnun,BETTINA E. BAUER,Christoph Schüller,Hubert Wolfger,Kostas Hatzixanthis,Mehdi Mollapour,Christa Gregori,Peter W. Piper,Karl Kuchler
标识
DOI:10.1128/mcb.23.5.1775-1785.2003
摘要
The Saccharomyces cerevisiae ATP-binding cassette (ABC) transporter Pdr12p effluxes weak acids such as sorbate and benzoate, thus mediating stress adaptation. In this study, we identify a novel transcription factor, War1p, as the regulator of this stress adaptation through transcriptional induction of PDR12. Cells lacking War1p are weak acid hypersensitive, since they fail to induce Pdr12p. The nuclear Zn2Cys6 transcriptional regulator War1p forms homodimers and is rapidly phosphorylated upon sorbate stress. The appearance of phosphorylated War1p isoforms coincides with transcriptional activation of PDR12. Promoter deletion analysis identified a novel cis-acting weak acid response element (WARE) in the PDR12 promoter required for PDR12 induction. War1p recognizes and decorates the WARE both in vitro and in vivo, as demonstrated by band shift assays and in vivo footprinting. Importantly, War1p occupies the WARE in the presence and absence of stress, demonstrating constitutive DNA binding in vivo. Our results suggest that weak acid stress triggers phosphorylation and perhaps activation of War1p. In turn, War1p activation is necessary for the induction of PDR12 through a novel signal transduction event that elicits weak organic acid stress adaptation.
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