Millwood I Y, Bihoreau M T, Gauguier D, Hyne G, Levy E R, Kreutz R, Lathrop G M, Monaco A P
Wellcome Trust Centre for Human Genetics, University of Oxford, Headington, United Kingdom.
Genomics. 1997 Mar 1;40(2):253-61. doi: 10.1006/geno.1996.4555.
We have constructed a gene-based genetic linkage map of the rat X chromosome. Fifteen polymorphic microsatellite markers associated with 13 different X chromosome genes have been isolated and genotyped on F2 progency from five different intercrosses. These markers have been integrated with 23 further rat X chromosome markers, resulting in a single linkage group for the X chromosome containing 38 microsatellite markers associated with 21 different genes and spanning a genetic distance of 88 cM. Fluorescence in situ hybridization was used to confirm the gene order obtained for the new markers and also placed 2 further genes, Hprt and Fmr1, on the map. Comparisons of gene order among rat, mouse, and human indicate homologous regions of conserved synteny and regions where evolutionary breakpoints have occurred. The genes from human Xq are conserved in order on the rat X chromosome, whereas those from human Xp have been rearranged into at least four conserved segments. The polymorphic markers and comparative map will be useful in studies on rat models of genetic disease.
我们构建了大鼠X染色体的基于基因的遗传连锁图谱。已从五个不同的杂交组合的F2后代中分离出与13个不同X染色体基因相关的15个多态微卫星标记并进行基因分型。这些标记已与另外23个大鼠X染色体标记整合,形成了一个X染色体的单一连锁群,其中包含与21个不同基因相关的38个微卫星标记,跨越88厘摩的遗传距离。荧光原位杂交用于确认新标记获得的基因顺序,并将另外两个基因Hprt和Fmr1定位到图谱上。大鼠、小鼠和人类之间基因顺序的比较表明了保守同线性的同源区域以及发生进化断点的区域。人类Xq的基因在大鼠X染色体上按顺序保守,而人类Xp的基因已重排为至少四个保守区段。这些多态性标记和比较图谱将有助于遗传疾病大鼠模型的研究。