Vincent A, Kretz C, Oberlé I, Mandel J L
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire et de Génie Génétique de l'INSERM, Faculté de Médecine, Strasbourg, France.
Hum Genet. 1989 Apr;82(1):85-6. doi: 10.1007/BF00288280.
We have isolated an X chromosome probe, St35.691 (DXS305), which detects two RFLPs with TaqI and PstI, whose combined heterozygosity is about 60%. This probe has been assigned to Xq28 by physical and genetic mapping and is very closely linked to DXS52, DXS15, and the coagulation factor VIII gene (F8C). The best estimate of the recombination fraction for the DXS52-DXS305 interval is 0.014, with a lod score of 50.1. Multipoint analysis places DXS305 on the same side of F8C as DXS52, but complete ordering of the three loci was not possible with our present data. This highly informative marker should be useful in the precise mapping of the many disease genes that have been assigned to the Xq28 band.
我们分离出了一个X染色体探针St35.691(DXS305),它用TaqI和PstI可检测到两个限制性片段长度多态性(RFLP),其联合杂合度约为60%。通过物理和遗传作图,该探针已被定位到Xq28,并且与DXS52、DXS15和凝血因子VIII基因(F8C)紧密连锁。DXS52 - DXS305区间重组率的最佳估计值为0.014,对数优势(lod)分数为50.1。多点分析表明DXS305与DXS52位于F8C的同一侧,但根据我们目前的数据无法确定这三个位点的完整顺序。这个信息丰富的标记对于精确定位已被定位到Xq28带的许多疾病基因应该是有用的。