Kramer R A, Andersen N
Proc Natl Acad Sci U S A. 1980 Nov;77(11):6541-5. doi: 10.1073/pnas.77.11.6541.
A library of DNA from the yeast, Saccharomyces cerevisiae, was constructed in phage lambda Charon 4 vector and then screened by differential plaque filter hybridization for genes induced by phosphate starvation. Two EcoRI fragments of 7.9 and 5.0 kilobase pairs that contained such genes were isolated. These cloned fragments may each carry one of the several copies of the genes for the repressible acid phosphatase of yeast. The fragments were use to examine mRNA levels of these genes in regulatory mutants of acid phosphatase.
构建了来自酿酒酵母的DNA文库,该文库采用噬菌体λCharon 4载体,然后通过差异噬菌斑滤膜杂交筛选受磷酸盐饥饿诱导的基因。分离出了两个分别含有此类基因的7.9千碱基对和5.0千碱基对的EcoRI片段。这些克隆片段可能各自携带酵母可阻遏酸性磷酸酶基因的多个拷贝之一。这些片段用于检测酸性磷酸酶调控突变体中这些基因的mRNA水平。