Arveiler B, Oberlé I, Mandel J L
U.184 INSERM, Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Faculté de Médecine, Strasbourg, France.
Genomics. 1987 Sep;1(1):60-6. doi: 10.1016/0888-7543(87)90105-4.
We have ordered nine polymorphic DNA markers within detailed map of the proximal part of the human X chromosome long arm, extending from band q11 to q22, by use of both physical mapping with a panel of rodent-human somatic hybrids and multipoint linkage analysis. Analysis of 44 families (including 17 families from the Centre d'Etude du Polymorphisme Humain) provided highly significant linkage data for both order and estimation of map distances between loci. We have obtained the following order: DXS1-DXS159-DXYS1-DXYS12-DXS3-(DXS94 , DXS178)-DXYS17. The most probable location of DXYS2 is between DXS159 and DXS3, close to DXYS1 and DXYS12. The high density of markers (nine loci within 30 recombination units) and the improvement in the estimation of recombination frequencies should be very useful for multipoint mapping of disease loci in this region and for diagnostic applications.
我们利用一组啮齿动物-人类体细胞杂种进行物理图谱构建以及多点连锁分析,在人类X染色体长臂近端从q11带至q22带的详细图谱内定位了9个多态性DNA标记。对44个家系(包括来自人类多态性研究中心的17个家系)的分析为基因座之间的顺序及图谱距离估计提供了高度显著的连锁数据。我们得到了以下顺序:DXS1-DXS159-DXYS1-DXYS12-DXS3-(DXS94, DXS178)-DXYS17。DXYS2最可能的位置在DXS159和DXS3之间,靠近DXYS1和DXYS12。标记的高密度(30个重组单位内有9个基因座)以及重组频率估计的改进对于该区域疾病基因座的多点定位及诊断应用应非常有用。