Mezzelani A, Zhang Y, Redaelli L, Castiglioni B, Leone P, Williams J L, Toldo S S, Wigger G, Fries R, Ferretti L
Istituto per la Difesa e la Valorizzazione del Germoplasma Animale, CNR, Milano, Italy.
Mamm Genome. 1995 Sep;6(9):629-35. doi: 10.1007/BF00352370.
Gene mapping in cattle has progressed rapidly in recent years largely owing to the introduction of powerful genetic markers, such as the microsatellites, and through advances in physical mapping techniques such as synteny mapping and fluorescence in situ hybridization (FISH). Microsatellite markers are often not physically mapped because they are generally isolated from small insert plasmid libraries, which makes their chromosomal localization inefficient. In this report we describe the FISH mapping of a large group of cosmid-derived bovine microsatellite markers, as our contribution to the European mapping initiative, BovMap. One objective of BovMap is to develop a set of anchored loci for the cattle genome map. Two cosmid libraries were screened with probes corresponding to the (AC)n microsatellite motif. Positive clones were mapped by FISH, and then a subset was further analyzed by sequencing the region flanking the microsatellite repeat. In total, 58 clones were hybridized with chromosomes and identified loci on 22 of the 31 different bovine chromosomes. Three clones contained satellite DNA. Two or more markers were placed on 12 chromosomes. Sequencing of the microsatellites and flanking regions was performed directly from 43 cosmids, as previously reported (Ferretti et al. Anim. Genet. 25, 209-214, 1994). Primers were developed for 39 markers and used to describe the polymorphism associated with the corresponding loci.
近年来,牛的基因图谱绘制进展迅速,这主要归功于强大的遗传标记(如微卫星)的引入,以及物理图谱绘制技术(如同源序列图谱绘制和荧光原位杂交(FISH))的进步。微卫星标记通常没有进行物理图谱绘制,因为它们一般是从小插入质粒文库中分离出来的,这使得它们的染色体定位效率低下。在本报告中,我们描述了一大组黏粒衍生的牛微卫星标记的FISH图谱绘制,作为我们对欧洲图谱绘制计划BovMap的贡献。BovMap的一个目标是为牛基因组图谱开发一组锚定基因座。用与(AC)n微卫星基序对应的探针筛选了两个黏粒文库。通过FISH对阳性克隆进行图谱绘制,然后通过对微卫星重复序列侧翼区域进行测序,对一个子集进行进一步分析。总共58个克隆与染色体杂交,并在31条不同的牛染色体中的22条上鉴定出基因座。三个克隆包含卫星DNA。在12条染色体上放置了两个或更多标记。如先前报道(Ferretti等人,《动物遗传学》25,209 - 214,1994),直接从43个黏粒中对微卫星及其侧翼区域进行测序。为39个标记开发了引物,并用于描述与相应基因座相关的多态性。