Raizis A M, Eccles M R, Reeve A E
Biochemistry Department, University of Otago, Dunedin, New Zealand.
Biochem J. 1993 Jan 1;289 ( Pt 1)(Pt 1):133-9. doi: 10.1042/bj2890133.
The expression of insulin-like growth factor-II (IGF-II) has been observed previously in many human cancers. The human IGF-II P3 promoter has been shown by others to give rise to abundant 6.0 kb and 2.2 kb fetal transcripts which are expressed in a variety of both paediatric and adult tumours. In order to determine the mechanism by which the P3 promoter is controlled, the promoter was analysed in cell lines using chloramphenicol acetyltransferase (CAT) assay and DNAase I footprinting techniques. The data indicated that P3 is a complex promoter involving at least nine transcription factor binding sites. Furthermore, high levels of 5-methylcytosine detected in the P3 promoter of HeLa genomic DNA suggest that IGF-II gene expression may also be influenced by DNA methylation.
先前已在许多人类癌症中观察到胰岛素样生长因子-II(IGF-II)的表达。其他人已表明,人类IGF-II P3启动子可产生丰富的6.0 kb和2.2 kb胎儿转录本,这些转录本在多种儿科和成人肿瘤中均有表达。为了确定P3启动子的调控机制,使用氯霉素乙酰转移酶(CAT)测定法和DNA酶I足迹技术在细胞系中对该启动子进行了分析。数据表明,P3是一个复杂的启动子,至少涉及九个转录因子结合位点。此外,在HeLa基因组DNA的P3启动子中检测到高水平的5-甲基胞嘧啶,这表明IGF-II基因表达也可能受DNA甲基化影响。