Gregorová S, Mnuková-Fajdelová M, Trachtulec Z, Capková J, Loudová M, Hoglund M, Hamvas R, Lehrach H, Vincek V, Klein J, Forejt J
Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Prague.
Mamm Genome. 1996 Feb;7(2):107-13. doi: 10.1007/s003359900029.
We have generated a high-resolution genetic map, 0.071 cM per backcross animal, of the 13 cM T-H2 region of the mouse Chromosome (Chr) 17. The map contains two phenotypic loci, T and Hst1, 12 RFLP markers, and 24 microsatellite loci. The Hst1 gene was mapped to a chromosomal interval contained within a single 580-kb YAC clone. The FFEH11 YAC is 0.44 cM long and carries, besides the Hst1 gene, five polymorphic DNA markers and recombination breakpoints of six backcross animals. Two candidate genes for Hst1 were identified based on their location and testicular expression. These are Tbp and D17Ph4e. The submilliMorgan map of the T-H2 region revealed significant clustering of (CA)n loci. The clustering, if shown to be a common feature in the mouse genome, may cause gaps in the physical map of the mouse genome.
我们构建了小鼠第17号染色体(Chr)13厘摩(cM)的T - H2区域的高分辨率遗传图谱,每个回交动物的分辨率为0.071 cM。该图谱包含两个表型位点T和Hst1、12个限制性片段长度多态性(RFLP)标记以及24个微卫星位点。Hst1基因被定位到一个单一的580千碱基对(kb)酵母人工染色体(YAC)克隆所包含的染色体区间内。FFEH11 YAC长0.44 cM,除Hst1基因外,还携带五个多态性DNA标记以及六只回交动物的重组断点。基于Hst1的位置和睾丸表达,鉴定出两个候选基因,即Tbp和D17Ph4e。T - H2区域的亚毫摩图谱显示(CA)n位点存在显著聚类。如果这种聚类被证明是小鼠基因组的一个共同特征,可能会导致小鼠基因组物理图谱出现缺口。