Sawyer M H, Ostrove J M, Felser J M, Straus S E
Virology. 1986 Feb;149(1):1-9. doi: 10.1016/0042-6822(86)90081-4.
The varicella-zoster virus (VZV) deoxypyrimidine kinase (dPK) gene was mapped by transfection of cloned viral DNA fragments into thymidine kinase-deficient mouse L (LTK-) cells and subsequent biochemical transformation of these cells to the LTK+ phenotype. Such transforming activity was limited to the BamHI-H and EcoRI-D fragments of the VZV genome, which overlap by 2.2 kb between map units 0.50 and 0.52. Biochemically transformed cells were shown to contain a high copy number of viral DNA sequences that had integrated into the cellular DNA. Extracts of these cells showed a higher level of dPK activity than did extracts of parental LTK- cells. With the use of Northern hybridization analysis of transformed and VZV-infected cell RNAs, it was possible to tentatively assign a 1.8-kb transcript to the VZV dPK.
通过将克隆的病毒DNA片段转染到胸苷激酶缺陷型小鼠L(LTK-)细胞中,并随后将这些细胞生化转化为LTK+表型,对水痘带状疱疹病毒(VZV)脱氧嘧啶激酶(dPK)基因进行了定位。这种转化活性仅限于VZV基因组的BamHI-H和EcoRI-D片段,它们在图谱单位0.50至0.52之间重叠2.2 kb。生化转化细胞显示含有大量已整合到细胞DNA中的病毒DNA序列。这些细胞的提取物显示出比亲代LTK-细胞提取物更高水平的dPK活性。通过对转化细胞和VZV感染细胞的RNA进行Northern杂交分析,有可能初步将一个1.8 kb的转录本归属于VZV dPK。