Kolakowski L F, Schloesser M, Cooperman B S
University of Pennsylvania, Department of Chemistry, Philadelphia 19104.
Nucleic Acids Res. 1988 Nov 25;16(22):10441-52. doi: 10.1093/nar/16.22.10441.
The gene for Saccharomyces cerevisiae inorganic pyrophosphatase, PPA, has been cloned by hybridization of "long" oligonucleotide probes with both cDNA and genomic S. cerevisiae libraries. The nucleotide sequence of 1612 bp from a genomic subclone that includes the entire coding region gives a deduced amino acid sequence that has nine differences (out of a total of 286 residues) from the previously published amino acid sequence that was determined directly. The codon usage in PPA is as expected for a "highly expressed" yeast gene. The upstream region contains a poly dA/dT sequence that might comprise a constitutive promoter. The PPA gene appears to be present in a single copy within the S. cerevisiae genome and has been localized to chromosome II.
通过将“长”寡核苷酸探针与酿酒酵母的cDNA文库和基因组文库进行杂交,克隆出了酿酒酵母无机焦磷酸酶(PPA)的基因。来自一个包含完整编码区的基因组亚克隆的1612 bp核苷酸序列推导出的氨基酸序列,与之前直接测定的氨基酸序列相比,在总共286个残基中有9个差异。PPA中的密码子使用情况符合“高表达”酵母基因的预期。上游区域包含一个多聚dA/dT序列,可能构成一个组成型启动子。PPA基因似乎在酿酒酵母基因组中以单拷贝形式存在,并且已定位到第二条染色体上。