Antoine M, Wegmann B, Kiefer P
Ruhr-Universität Bochum, Medizinische Fakultät, Institut für Hygiene und Mikrobiologie, Abteilung für Med. Mikrobiol. und Virologie, Gebäude, Germany.
Virus Genes. 1998;17(2):157-68. doi: 10.1023/a:1008020808314.
Development of methods for gene transfer into specific cell types or tissues is important for experimental research as well as clinical therapeutical approaches. We report here the cloning and characterization of the envelope (env) gene and the U3 region of a retrovirus from an infected human Small Cell Lung Cancer (SCLC) cell line. The replication of this murine retrovirus is also fully supported by other lung cancer cell lines of different histological origin. We present evidence that a long terminal repeat (LTR)-beta-galactosidase (beta-Gal) reporter construct performed as well as an analogous cytomegalovirus (CMV) promoter beta-Gal construct in the human lung epithelial cell line A549 and in the human larynx carcinoma cell line HEp2.
开发将基因导入特定细胞类型或组织的方法对于实验研究以及临床治疗方法都很重要。我们在此报告了从受感染的人小细胞肺癌(SCLC)细胞系中克隆和鉴定一种逆转录病毒的包膜(env)基因和U3区域。这种鼠逆转录病毒的复制也得到了其他不同组织学来源的肺癌细胞系的充分支持。我们提供的证据表明,在人肺上皮细胞系A549和人喉癌细胞系HEp2中,一个长末端重复序列(LTR)-β-半乳糖苷酶(β-Gal)报告基因构建体的表现与类似的巨细胞病毒(CMV)启动子β-Gal构建体相同。