Macreadie I G, Horaitis O, Vaughan P R, Clark-Walker G D
CSIRO Division of Biomolecular Engineering, Parkville, Victoria, Australia.
Yeast. 1991 Feb;7(2):127-35. doi: 10.1002/yea.320070206.
Shuttle plasmids, pE1.CUP1B and pE1.CUP1E of 10.6 kb, have been constructed between the metallothionein-encoding CUP1 gene of Saccharomyces cerevisiae and a vector capable of replication in Kluyveromyces lactis. Introduction of these plasmids into K. lactis confers resistance to copper as well as to cadmium and silver. Resistance to these latter metal ions, in the absence of induction by copper, suggested that the CUP1 gene is constitutively expressed in the foreign background. Introduction of the lacZ reporter gene from Escherichia coli into a cloning site downstream from the CUP1 promoter showed that expression of this gene is constitutive in K. lactis but in S. cerevisiae induction by copper is necessary. Sequences upstream from the CUP1 promoter are involved in the constitutive expression since deletion of 91 nucleotides from this region abolishes metal resistance. It is suggested that a K. lactis protein, normally involved in activating transcription of the resident CUP1 gene in the presence of copper, can promote transcription in the absence of metal ion by binding to the upstream activation sequence of the introduced CUP1 gene.
穿梭质粒pE1.CUP1B和10.6 kb的pE1.CUP1E,构建于酿酒酵母金属硫蛋白编码基因CUP1与能够在乳酸克鲁维酵母中复制的载体之间。将这些质粒导入乳酸克鲁维酵母可赋予其对铜以及镉和银的抗性。在没有铜诱导的情况下对这些后两种金属离子具有抗性,这表明CUP1基因在异源背景中组成性表达。将来自大肠杆菌的lacZ报告基因导入CUP1启动子下游的克隆位点,结果表明该基因在乳酸克鲁维酵母中组成性表达,但在酿酒酵母中铜诱导是必需的。CUP1启动子上游的序列参与组成性表达,因为从该区域缺失91个核苷酸会消除金属抗性。有人提出,一种通常在有铜存在时参与激活常驻CUP1基因转录的乳酸克鲁维酵母蛋白,可通过与导入的CUP1基因的上游激活序列结合,在没有金属离子的情况下促进转录。