Blythe N L, Senior P V, Beck F
Howard Florey Institute of Experimental Physiology and Medicine, Parkville, Victoria, Australia.
J Anat. 1996 Feb;188 ( Pt 1)(Pt 1):65-74.
Insulin-like growth factor II (IGF-II) is expressed during embryogenesis in rodents and humans, but is not produced in most adult tissues. This pattern of expression is closely shared by the gene H19, which lies 3' to IGF-II. This, together with the fact that the genes are reciprocally imprinted, has led to the proposal that the genes are under common transcriptional control by the H19 enhancers during development. In the present study, embryonic stem (ES) cells have been used to generate teratocarcinomas in mice. These tumours generate a wide range of differentiated tissues which have been subjected to hybridisation histochemistry with RNA probes to H19 and IGF-II. Coexpression of the two genes was found in a range of tissues, a pattern consistent with the idea of common transcriptional control. However, there were some areas in which H19 was expressed strongly in comparison with IGF-II and vice versa suggesting the existence of further control elements other than the H19 enhancers.
胰岛素样生长因子II(IGF-II)在啮齿动物和人类的胚胎发育过程中表达,但在大多数成年组织中不产生。基因H19的表达模式与IGF-II极为相似,H19位于IGF-II的3'端。再加上这两个基因相互印记的事实,有人提出在发育过程中,这两个基因受H19增强子的共同转录调控。在本研究中,胚胎干细胞已被用于在小鼠体内生成畸胎瘤。这些肿瘤产生了多种分化组织,并用针对H19和IGF-II的RNA探针进行了杂交组织化学分析。在一系列组织中发现了这两个基因的共表达,这一模式与共同转录调控的观点一致。然而,有些区域H19的表达比IGF-II强,反之亦然,这表明除了H19增强子外,还存在其他调控元件。