Vaiman D, Mercier D, Eggen A, Bahri-Darwich I, Grohs C, Cribiu E P, Dolf G, Oustry A, Guérin G, Levéziel H
Laboratoire de Génétique biochimique et de Cytogénétique, INRA-CRJ, Jouy-en-Josas, France.
Mamm Genome. 1994 Sep;5(9):553-6. doi: 10.1007/BF00354929.
A genetic map of bovine Chromosome (Chr) 11 (BTA11, synteny group U16) has been constructed from 330 animals belonging to 21 families, which constitute the international bovine reference panel (IBRP). This map is based on 13 polymorphic microsatellite markers, two of which were chosen in previously published maps. Three markers have been isolated from cosmids. Two of the three cosmids have been physically localized by fluorescence in situ hybridization (FISH), to anchor the genetic map on the chromosome. In addition, a biallelic polymorphism in the beta-lactoglobulin gene (LGB) has been genetically positioned relative to the microsatellite markers. The most probable order of the markers is: cen-INRA044-BM716-INRA177-(TGLA327, INRA198, INRA131)-INRA111-INRABERN169-(INRA115, INRA032)-INRA108-INRABERN162-INRA195-LGB. The total linkage group spans 126 cM, which probably corresponds to most of the chromosome length. The average intermarker distance is about 10.5 cM, allowing the potential detection of a genetic linkage with any Economic Trait Loci (ETL) of this chromosome. Seven of these markers have been previously published by Vaiman and coworkers (1994), two will be published as part of a set of markers (Eggen et al. in preparation), two are described in this paper, and two (BM716, TGLA327) were chosen from the published maps of BTA11 in order to integrate our data with existing maps. All these markers were assigned to synteny group U16 by use of a previously characterized panel of hamster/bovine somatic hybrid cell lines (Guérin et al. 1994).(ABSTRACT TRUNCATED AT 250 WORDS)
利用属于21个家系的330头动物构建了牛11号染色体(BTA11,同线群U16)的遗传图谱,这些动物构成了国际牛参考面板(IBRP)。该图谱基于13个多态微卫星标记构建,其中两个标记选自先前发表的图谱。三个标记是从黏粒中分离出来的。三个黏粒中的两个已通过荧光原位杂交(FISH)进行了物理定位,以便将遗传图谱锚定到染色体上。此外,β-乳球蛋白基因(LGB)中的双等位基因多态性已相对于微卫星标记进行了遗传定位。标记的最可能顺序为:着丝粒-INRA044-BM716-INRA177-(TGLA327,INRA198,INRA131)-INRA111-INRABERN169-(INRA115,INRA032)-INRA108-INRABERN162-INRA195-LGB。总的连锁群跨度为126厘摩,这可能对应于该染色体的大部分长度。标记间的平均距离约为10.5厘摩,这使得有可能检测到与该染色体上任何经济性状位点(ETL)的遗传连锁。这些标记中有7个先前已由Vaiman及其同事发表(1994年),2个将作为一组标记的一部分发表(Eggen等人正在准备),2个在本文中描述,还有2个(BM716,TGLA327)是从已发表的BTA11图谱中选取的,以便将我们的数据与现有图谱整合。所有这些标记通过使用先前鉴定的仓鼠/牛体细胞杂种细胞系面板(Guérin等人,1994年)被分配到同线群U16。(摘要截短于250字)