Vaughn J C, Whitman D J, Bagshaw J C, Helder J C
Biochim Biophys Acta. 1982 May 31;697(2):156-61. doi: 10.1016/0167-4781(82)90071-9.
A library of genomic DNA from the brine shrimp, Artemia, has been constructed with the Charon 4A phage vector, utilizing EcoRI passenger fragments. Screening this library with purified Xenopus laevis cloned rDNA genes has resulted in the identification and plaque purification of a recombinant containing a complete Artemia (18 S + 26 S) rDNA repeat unit. A physical map derived from the analysis of restriction endonuclease digests of the repeat unit, which measures 13.9 kilobase pairs, is similar to the map derived from genomic DNA. In common with several other species, the 26 S rRNA gene terminates with a HindIII recognition site.
利用EcoRI插入片段,用Charon 4A噬菌体载体构建了卤虫基因组DNA文库。用纯化的非洲爪蟾克隆rDNA基因筛选该文库,已鉴定并进行了噬菌斑纯化,得到一个含有完整卤虫(18S + 26S)rDNA重复单元的重组体。对长度为13.9千碱基对的重复单元进行限制性内切酶消化分析得到的物理图谱,与从基因组DNA得到的图谱相似。与其他几个物种一样,26S rRNA基因以一个HindIII识别位点终止。