Tomilin N V, Podgornaia O I, Abramian D S, Glebov O K
Tsitologiia. 1985 May;27(5):554-64.
Chinese hamster A238 TK- -cells were transformed with plasmids (derivatives of pBR325) containing thymidine kinase (TK) gene of Herpes simplex virus type 1 (HSV1). The results of dot- and blot-hybridization indicate the presence of pBR325 sequences in the chromosomal fractions of DNA in the transformant clones. These sequences are probably tandemly arranged, and each cluster contains 25--50 copies. SV40 sequences cloned in pBR325 were introduced into the Chinese hamster cells by co-transformation with TK-gene of HSV1-containing plasmid DNA, and all the co-transformant clones selected for TK+-phenotype were shown by hydridization to contain 3V40 DNA fragments. Isoelectrofocusing in polyacrylamide gel shows that thymidine kinase from TK+-transformant clones is of viral type (isoelectric point 7), in contrast to the cellular enzyme (coded by chromosomal gene) having alkaline isoelectric point (pH 9). The results suggest that the true TK+-transformant cells are selected by the procedure used in this study.
用含有1型单纯疱疹病毒(HSV1)胸苷激酶(TK)基因的质粒(pBR325的衍生物)转化中国仓鼠A238 TK⁻细胞。斑点杂交和印迹杂交结果表明,转化克隆的DNA染色体组分中存在pBR325序列。这些序列可能是串联排列的,每个簇包含25 - 50个拷贝。通过与含HSV1 TK基因的质粒DNA共转化,将克隆在pBR325中的SV40序列导入中国仓鼠细胞,通过杂交显示,所有选择的具有TK⁺表型的共转化克隆都含有SV40 DNA片段。在聚丙烯酰胺凝胶中进行等电聚焦显示,与具有碱性等电点(pH 9)的细胞酶(由染色体基因编码)相比,来自TK⁺转化克隆的胸苷激酶是病毒型的(等电点7)。结果表明,本研究中使用的方法筛选出了真正的TK⁺转化细胞。