Vignaux F, Priat C, Jouquand S, Hitte C, Jiang Z, Chéron A, Renier C, André C, Galibert F
UPR 41 CNRS Recombinaisons Génétiques, Faculté de Médecine, Rennes, France.
J Hered. 1999 Jan-Feb;90(1):62-7. doi: 10.1093/jhered/90.1.62.
Dog fibroblasts grown from a biopsy performed in a male mongrel were fused after gamma irradiation with thymidine kinase-deficient hamster cells and cultivated in selection medium. A total of 148 clones were obtained and screened by means of PCR amplification using primers corresponding to a dog-specific short repetitive element and to dog microsatellites and genes. One hundred seven cell lines were selected and grown in roller bottles and the distribution of 39 markers was analyzed in the extracted DNA. The results clearly indicate that this panel of hybrid cell lines should prove invaluable for constructing a map of the canine genome. In parallel, for more than 500 microsatellites present in the databases or screened from two libraries of short inserts, we have determined PCR conditions favoring dog-specific products even in the presence of hamster DNA. These highly polymorphic microsatellites should be useful in further linkage studies. We have also characterized 254 markers: dog genes, human expressed sequenced tags (huESTs), and traced orthologous amplified sequenced tags (TOASTs). Once mapped, these will constitute powerful tools to detect regions of conserved synteny in human and other mammalian genomes.
从一只雄性杂种狗活检组织中培养出的犬成纤维细胞,经γ射线照射后与胸腺嘧啶激酶缺陷型仓鼠细胞融合,并在选择培养基中培养。共获得148个克隆,并使用与犬特异性短重复元件、犬微卫星和基因对应的引物,通过PCR扩增进行筛选。选择了107个细胞系在滚瓶中培养,并对提取的DNA中的39个标记物的分布进行了分析。结果清楚地表明,这组杂交细胞系对于构建犬基因组图谱将被证明具有极高的价值。同时,对于数据库中存在的或从两个短插入文库中筛选出的500多个微卫星,我们已经确定了即使在存在仓鼠DNA的情况下也有利于产生犬特异性产物的PCR条件。这些高度多态性的微卫星在进一步的连锁研究中应该会有用。我们还对254个标记物进行了表征:犬基因、人类表达序列标签(huESTs)和追踪直系同源扩增序列标签(TOASTs)。一旦定位,这些将构成检测人类和其他哺乳动物基因组中保守同线性区域的有力工具。