Guarente L, Mason T
Cell. 1983 Apr;32(4):1279-86. doi: 10.1016/0092-8674(83)90309-4.
We show that expression of the iso-1-cytochrome c gene of Saccharomyces cerevisiae, CYC1, is tightly regulated by levels of intracellular heme. Expression is reduced at least 200-fold in cells grown under conditions of heme deficiency. Studies on the regulation of a CYC1-lacZ fused gene and direct determination of mRNA levels indicate that this control is transcriptional. Furthermore, we show that the heme regulatory site in the CYC1 promoter region is an upstream activation site (UASc) centered about 275 bp upstream from the region of transcriptional initiation. The latter region is required for optimal transcription and contains three TATA box sequences and six prominent mRNA initiation sites that span 34 bp. Substitution of the UASc with the UAS of the yeast GAL10 gene results in activation of the normal set of CYC1 transcripts. In this case, however, transcription is independent of regulation by heme, suggesting that in the wildtype, heme controls initiation per se and not translation or mRNA stability.
我们发现,酿酒酵母的同工型1-细胞色素c基因CYC1的表达受细胞内血红素水平的严格调控。在血红素缺乏条件下生长的细胞中,其表达至少降低200倍。对CYC1-lacZ融合基因调控的研究以及对mRNA水平的直接测定表明,这种调控是转录水平的。此外,我们表明CYC1启动子区域中的血红素调控位点是一个上游激活位点(UASc),位于转录起始区域上游约275 bp处。后一个区域是最佳转录所必需的,包含三个TATA盒序列和六个跨越34 bp的突出mRNA起始位点。用酵母GAL10基因的UAS替代UASc会导致正常CYC1转录本的激活。然而,在这种情况下,转录不受血红素调控,这表明在野生型中,血红素控制的是起始本身,而不是翻译或mRNA稳定性。