Zaman Z, Brown A J, Dawes I W
Institute of Cell and Molecular Biology, University of Edinburgh, UK.
Mol Microbiol. 1992 Jan;6(2):239-46. doi: 10.1111/j.1365-2958.1992.tb02005.x.
A well-defined set of isogenic yeast strains has been constructed whereby each strain contains a different LPD::lacZ gene fusion integrated at the ura3 locus. These LPD::lacZ fusions differ in the amount of the LPD1 gene (encoding lipoamide dehydrogenase) that is fused to the lacZ reporter. Comparison of the beta-galactosidase activities of each strain during growth on glucose or ethanol revealed that some part of the LPD1 coding region between +13 and +700 is involved in activating gene expression in a carbon source-dependent manner. This activation occurs at the mRNA level, and is not mediated by changes in mRNA stability. Therefore, the LPD1 gene appears to contain a transcriptional enhancer that lies 3' to the transcriptional start site, and which responds to carbon source.
已构建了一组明确的同基因酵母菌株,其中每个菌株都含有整合在ura3位点的不同LPD::lacZ基因融合体。这些LPD::lacZ融合体在与lacZ报告基因融合的LPD1基因(编码硫辛酰胺脱氢酶)的量上有所不同。比较每个菌株在葡萄糖或乙醇上生长期间的β-半乳糖苷酶活性发现,LPD1编码区在+13至+700之间的某些部分以碳源依赖的方式参与激活基因表达。这种激活发生在mRNA水平,并且不是由mRNA稳定性的变化介导的。因此,LPD1基因似乎包含一个位于转录起始位点3'端且对碳源有反应的转录增强子。