Omura F, Fujita A, Shibano Y
Institute for Fundamental Research, Suntory Ltd., Osaka, Japan.
FEBS Lett. 1996 Jun 3;387(2-3):179-83. doi: 10.1016/0014-5793(96)00486-3.
Transcription of MET genes in Saccharomyces cerevisiae depends on a transcriptional activator, the MET4 gene product (Met4p). Using in vitro mutagenesis, we isolated two mutant MET4 alleles encoding [Pro215]Met4p and [Ser156]Met4p. These mutations impeded Met4p's responsiveness to methionine in the media, and yeast cells carrying mutant alleles exhibited enhanced transcription of MET genes under repressing conditions. The enhanced transcription was dependent on the CBF1 gene, but did not compete with an excess of wild-type Met4p, suggesting that some changes in the affinity of Met4p to other factors might be involved in S-adenosylmethionine-mediated transcriptional regulation.
酿酒酵母中MET基因的转录依赖于一种转录激活因子,即MET4基因产物(Met4p)。通过体外诱变,我们分离出了两个编码[Pro215]Met4p和[Ser156]Met4p的突变MET4等位基因。这些突变阻碍了Met4p对培养基中蛋氨酸的反应,携带突变等位基因的酵母细胞在抑制条件下表现出MET基因转录增强。增强的转录依赖于CBF1基因,但不与过量的野生型Met4p竞争,这表明Met4p与其他因子亲和力的某些变化可能参与了S-腺苷甲硫氨酸介导的转录调控。