Morizot D C, McEntire B B, Della Coletta L, Kazianis S, Schartl M, Nairn R S
The University of Texas M.D. Anderson Cancer Center, Science Park-Research Division, Smithville 78957, USA.
Mol Carcinog. 1998 Jul;22(3):150-7. doi: 10.1002/(sici)1098-2744(199807)22:3<150::aid-mc2>3.0.co;2-p.
Xiphophorus fish have been the subject of intensive genetic research for more than 60 yr, primarily because of the availability of a number of interspecific hybrids that are malignant melanoma models with apparently simple oncogene and tumor suppressor gene determinants. The gene map of Xiphophorus is one of the most extensive among nonhuman vertebrates, with about 100 genes assigned to at least 20 independently assorting linkage groups (LGs), as well as more than 250 anonymous DNA sequence markers, providing coverage for most of the genome for genetic mapping studies. This characteristic has resulted in the mapping of a tumor suppressor locus, DIFF, which is one of two genetic determinants of melanoma formation in the best-studied hybrid melanoma, the Gordon-Kosswig melanoma model. The other gene responsible for melanoma formation in this model is a sex-linked tyrosine kinase gene related to EGFR and called Xiphophorus melanoma receptor kinase (Xmrk). The cellular oncogene homologues of the non-receptor tyrosine kinase family orthologous toyes and fyn have also been found to be overexpressed in malignant melanomas of Xiphophorus and may be involved in tumor progression. We report here the map location of a Xiphophorus yes gene, YES1, in LG VI, closest to the EGFR gene and the assignment of a fyn gene homologue to newly designated LG XV, linked to the gene for cytosolic alpha-galactosidase. We also confirmed that an EGFR-related sequence (EGFRL1) that we previously assigned to Xiphophorus LG VI by cross-hybridization to a viral erbB probe was the EGFR orthologue. Our results suggest that the presence of expressed duplicates of members of the tyrosine kinase gene family in teleost fishes may increase the potential number of targets in oncogenic cascades in fish tumor models.
剑尾鱼作为深入遗传学研究的对象已有60多年,主要是因为有许多种间杂种,它们是恶性黑色素瘤模型,其癌基因和肿瘤抑制基因决定因素看似简单。剑尾鱼的基因图谱是所有非人类脊椎动物中最详尽的图谱之一,约有100个基因被定位到至少20个独立分配的连锁群(LGs)上,还有250多个匿名DNA序列标记,为大多数基因组的遗传图谱研究提供了覆盖范围。这一特性使得一个肿瘤抑制基因座DIFF得以定位,DIFF是在研究最深入的杂种黑色素瘤——戈登 - 科斯维格黑色素瘤模型中,黑色素瘤形成的两个遗传决定因素之一。该模型中另一个导致黑色素瘤形成的基因是一个与表皮生长因子受体(EGFR)相关的性连锁酪氨酸激酶基因,称为剑尾鱼黑色素瘤受体激酶(Xmrk)。与yes和fyn直系同源的非受体酪氨酸激酶家族的细胞癌基因同源物,也被发现在剑尾鱼的恶性黑色素瘤中过度表达,可能参与肿瘤进展。我们在此报告剑尾鱼yes基因YES1在LG VI中的图谱位置,它最靠近EGFR基因,以及将一个fyn基因同源物定位到新命名的LG XV上,该LG与胞质α - 半乳糖苷酶基因相连。我们还证实,我们之前通过与病毒erbB探针杂交而定位到剑尾鱼LG VI上的一个与EGFR相关的序列(EGFRL1)是EGFR的直系同源物。我们的结果表明,硬骨鱼类酪氨酸激酶基因家族成员的表达重复的存在,可能会增加鱼类肿瘤模型致癌级联反应中潜在的靶点数量。