Bell J A, Rinchik E M, Raymond S, Suffolk R, Jackson I J
MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
Mamm Genome. 1995 Jun;6(6):389-95. doi: 10.1007/BF00355638.
For over 40 years germ-cell mutagenesis experiments have generated many new mutations at the brown (b or Tyrp1) locus on mouse Chromosome (Chr) 4. These mutations, many of which are deletions, were recovered by the specific-locus mutagenesis technique. Previous analysis of a panel of brown deletions, generated at Oak Ridge, has enabled both a preliminary molecular and a functional map around the locus to be generated. We have used a panel of hybrid DNA from 25 Oak Ridge deletions, where the deleted chromosome was heterozygous with a Mus spretus chromosome, to map polymorphic markers including microclones, microsatellites, and cloned DNA markers. We have generated a fine structure map, based on 25 new markers, of an 8.5-cM region surrounding the brown locus. This map will prove useful in future mapping studies of this region and in the isolation of the genes that lie within it.
40多年来,生殖细胞诱变实验在小鼠4号染色体上的棕色(b或Tyrp1)位点产生了许多新的突变。这些突变,其中许多是缺失突变,是通过特定位点诱变技术获得的。先前对在橡树岭产生的一组棕色缺失突变进行的分析,使得能够围绕该位点生成初步的分子图谱和功能图谱。我们使用了来自25个橡树岭缺失突变的一组杂交DNA,其中缺失的染色体与斯氏小家鼠染色体杂合,以定位包括微克隆、微卫星和克隆DNA标记在内的多态性标记。我们基于25个新标记生成了棕色位点周围8.5厘摩区域的精细结构图谱。该图谱将证明在该区域未来的定位研究以及该区域内基因的分离中很有用。