Lewis J A
Mol Cell Biol. 1986 Jun;6(6):1998-2010. doi: 10.1128/mcb.6.6.1998-2010.1986.
My colleagues and I have cloned a nearly full-length Chinese hamster thymidine kinase (TK) cDNA in a lambda gt10 vector and characterized this cDNA by nucleotide sequencing. The hamster TK protein is encoded in this cDNA by a 702-base-pair open reading frame which specifies a 25,625-dalton protein closely homologous to the previously described human and chicken TK proteins. Using cDNA nucleotide sequence data in conjunction with sequence data derived from selected subclones of the hamster TK gene recombinant phage lambda HaTK.5, we have resolved the structure of the TK gene, finding the 1,219 base pairs of the cDNA sequence to be distributed through 11.2 kilobases of genomic DNA in at least seven exon segments. In addition, we have constructed a variety of Chinese hamster TK minigenes and exonuclease III-S1 derivatives of these genes which have permitted us to define the limits of the Chinese hamster TK gene promoter and demonstrate that efficient TK transformation of Ltk- cells by TK minigenes depends on the presence of both TK intervening sequences and sequences 3' to the site of mRNA polyadenylation.
我和我的同事在λgt10载体中克隆了一个近乎全长的中国仓鼠胸苷激酶(TK)cDNA,并通过核苷酸测序对该cDNA进行了表征。仓鼠TK蛋白由这个cDNA中的一个702个碱基对的开放阅读框编码,该开放阅读框指定了一个25,625道尔顿的蛋白,与先前描述的人类和鸡的TK蛋白密切同源。利用cDNA核苷酸序列数据以及来自仓鼠TK基因重组噬菌体λHaTK.5的选定亚克隆的序列数据,我们解析了TK基因的结构,发现cDNA序列的1219个碱基对分布在至少7个外显子片段中的11.2千碱基的基因组DNA中。此外,我们构建了多种中国仓鼠TK微型基因以及这些基因的核酸外切酶III-S1衍生物,这使我们能够确定中国仓鼠TK基因启动子的界限,并证明TK微型基因对Ltk-细胞的有效TK转化取决于TK间隔序列和mRNA聚腺苷酸化位点3'端序列的存在。