Dimitrijevic N, Winkler C, Wellbrock C, Gómez A, Duschl J, Altschmied J, Schartl M
Physiological Chemistry I, Theodor Boveri Institute for Biosciences (Biocenter), University of Würzburg, Germany.
Oncogene. 1998 Apr 2;16(13):1681-90. doi: 10.1038/sj.onc.1201693.
Xmrk is a receptor tyrosine kinase closely related to the human EGF receptor. In the teleost fish Xiphophorus two versions of the Xmrk gene exist, an oncogene (ONC) and a proto-oncogene (INV). While ONC-Xmrk is the melanoma-inducing gene, INV-Xmrk appears not to be involved in transformation of pigment cells. To elucidate the mechanism that converts the proto-oncogene into a transforming oncogene a comparative analysis of the structure, expression and function of both versions of the gene was performed. In contrast to ONC-Xmrk which is expressed at high levels in melanoma cells, the proto-oncogene INV-Xmrk is ubiquitously expressed at very low levels indicating overexpression as one possible reason for tumorigenicity by ONC-Xmrk. As sequence comparison of the proto-oncogene and the oncogene revealed a number of amino acid changes, a possible effect of these mutations on the activation of the ONC-Xmrk receptor was determined. A constitutive activation of the oncogenic receptor was found and ectopic expression of INV-Xmrk after microinjection into medakafish embryos did not lead to the high tumour rate in transgenic fish as observed for the oncogene. Our data therefore suggest that overexpression of the receptor alone is not sufficient for melanoma induction, but that in addition activating mutations in ONC-Xmrk are responsible for its full tumorigenic potential.
Xmrk是一种与人类表皮生长因子受体密切相关的受体酪氨酸激酶。在硬骨鱼剑尾鱼属中,存在两种版本的Xmrk基因,一种是癌基因(ONC),另一种是原癌基因(INV)。虽然ONC-Xmrk是诱导黑色素瘤的基因,但INV-Xmrk似乎不参与色素细胞的转化。为了阐明将原癌基因转化为转化癌基因的机制,对该基因的两个版本的结构、表达和功能进行了比较分析。与在黑色素瘤细胞中高水平表达的ONC-Xmrk不同,原癌基因INV-Xmrk在极低水平上普遍表达,这表明过表达是ONC-Xmrk致瘤性的一个可能原因。由于原癌基因和癌基因的序列比较揭示了一些氨基酸变化,因此确定了这些突变对ONC-Xmrk受体激活的可能影响。发现致癌受体存在组成型激活,并且将INV-Xmrk显微注射到青鳉胚胎中后其异位表达并未导致转基因鱼出现如癌基因所观察到的高肿瘤发生率。因此,我们的数据表明,仅受体的过表达不足以诱导黑色素瘤,此外,ONC-Xmrk中的激活突变才是其完全致瘤潜力的原因。