Lin P F, Zhao S Y, Ruddle F H
Proc Natl Acad Sci U S A. 1983 Nov;80(21):6528-32. doi: 10.1073/pnas.80.21.6528.
In this report, we describe the cloning of the human cytoplasmic thymidine kinase (tk-C; EC 2.7.1.21) gene and its preliminary characterization. The tk-C sequences were isolated from a phage genomic library made from DNA of a transfected mouse cell carrying the human tk-C gene. The human transforming sequences were identified by homology with human Alu sequences. Six recombinant phages were isolated and five were competent to transfer human TK-C activity to TK-deficient mouse cells when transferred in pairs. Conclusively, sequences homologous to these clones are present in all human TK+ transformants examined. We estimate the maximal size of the tk-C gene to be 14 kilobase pairs and its minimal size to be between 4 and 5 kilobase pairs. The gene contains many noncoding inserts and numerous Alu sequences.
在本报告中,我们描述了人细胞质胸苷激酶(tk-C;EC 2.7.1.21)基因的克隆及其初步特征。tk-C序列是从一个噬菌体基因组文库中分离出来的,该文库由携带人tk-C基因的转染小鼠细胞的DNA构建而成。通过与人Alu序列的同源性鉴定出人转化序列。分离出6个重组噬菌体,其中5个在成对转移时能够将人TK-C活性转移到TK缺陷的小鼠细胞中。最终,在所检测的所有人类TK+转化体中都存在与这些克隆同源的序列。我们估计tk-C基因的最大大小为14千碱基对,最小大小在4至5千碱基对之间。该基因包含许多非编码插入片段和大量Alu序列。