Coleman T A, Hou Y T, Kopchick J J
Department of Zoological and Biomedical Sciences, Ohio University, Athens 45701.
Gene. 1991 Oct 15;106(2):243-8. doi: 10.1016/0378-1119(91)90205-p.
The chloramphenicol acetyltransferase-encoding reporter gene (cat) is used extensively in assessing the ability of transcriptional regulatory elements (TRE) to direct gene expression in eukaryotic cells. Two commonly utilized plasmids contain the cat coding sequences under the transcriptional control of the Rous sarcoma virus LTR (pRSVcat) or simian virus 40 early (SV40E) promoter (pSV2cat). In the present study, we have recloned the RSV-LTR and SV40E TRE into a pUC18 vector. Direct comparison of these TRE in different plasmid vectors, as well as reevaluation of their relative level of cat expression revealed: (1) a small but significant increases in SV40E-directed reporter gene expression was observed when the TRE was inserted into the pUC18 vector; and (2) a significant increase in SV40E-directed gene expression was realized by inclusion of the 69-bp 5' of the sequences present in pSV2cat. These distal sequences are required for maximal activity of the SV40 TRE in the cell lines tested.
编码氯霉素乙酰转移酶的报告基因(cat)被广泛用于评估转录调控元件(TRE)在真核细胞中指导基因表达的能力。两种常用的质粒含有在劳斯肉瘤病毒长末端重复序列(pRSVcat)或猿猴病毒40早期(SV40E)启动子(pSV2cat)转录控制下的cat编码序列。在本研究中,我们已将RSV-LTR和SV40E TRE重新克隆到pUC18载体中。对这些TRE在不同质粒载体中的直接比较,以及对它们相对cat表达水平的重新评估显示:(1)当TRE插入pUC18载体时,观察到SV40E指导的报告基因表达有微小但显著的增加;(2)通过包含pSV2cat中存在的序列的69个碱基对的5'端,实现了SV40E指导的基因表达的显著增加。这些远端序列是测试细胞系中SV40 TRE最大活性所必需的。