Jeyaprakash A, Welch J W, Fogel S
Department of Plant Biology, University of California, Berkeley 94720.
Mol Gen Genet. 1991 Mar;225(3):363-8. doi: 10.1007/BF00261675.
A 3.3 kb fragment of yeast genomic DNA was isolated by screening a genomic library constructed in the high copy number 2 micron plasmid YEp351 vector for clones capable of enhancing the degree of resistance of Saccharomyces cerevisiae strain MW3070-8B to cadmium. The insert contained two complete copies of the CUP1 gene open reading frame (183 bp), including the upstream promoter sequences (450 bp) with two conserved metal responsive cis-acting elements. Northern analysis showed that addition of cadmium (0.02 microM) or copper (50 microM) to overnight liquid cultures of yeast induced expression of CUP1 transcripts from both chromosomal and plasmid-borne gene copies. The cloned 3.3 kb DNA in a high copy number plasmid restored copper resistance to the sensitive strain LS70-3B delta, deleted for the CUP1 gene (cup 1 delta), but failed to restore cadmium resistance. Thus, CUP1 gene expression in yeast appears to be influenced differently by cadmium and copper ions. Resistance to heavy metal poisoning resulted from enhanced gene product levels attributable to amplification of the CUP1 gene as well as to increased transcriptions. Two distinct gene product levels mediate cadmium and copper resistance; a higher gene product level was required to confer cadmium resistance.
通过筛选构建于高拷贝数2微米质粒YEp351载体中的基因组文库,分离出一段3.3 kb的酵母基因组DNA片段,以寻找能够增强酿酒酵母菌株MW3070 - 8B对镉抗性程度的克隆。该插入片段包含CUP1基因开放阅读框(183 bp)的两个完整拷贝,包括带有两个保守金属反应性顺式作用元件的上游启动子序列(450 bp)。Northern分析表明,向酵母过夜液体培养物中添加镉(0.02 microM)或铜(50 microM)可诱导来自染色体和质粒携带基因拷贝的CUP1转录本表达。高拷贝数质粒中克隆的3.3 kb DNA恢复了对缺失CUP1基因(cup 1 delta)的敏感菌株LS70 - 3B delta的铜抗性,但未能恢复镉抗性。因此,酵母中CUP1基因的表达似乎受到镉和铜离子的不同影响。对重金属中毒的抗性源于CUP1基因扩增以及转录增加导致的基因产物水平提高。两种不同的基因产物水平介导镉和铜抗性;赋予镉抗性需要更高的基因产物水平。