Coleman M, Bhattacharya S, Lindsay S, Wright A, Jay M, Litt M, Craig I, Davies K
Institute of Molecular Medicine, University of Oxford, England.
Am J Hum Genet. 1990 Dec;47(6):935-40.
The microsatellite marker DXS426 maps to the interval Xp21.1-Xp11.21, the chromosomal region which contains two loci for X-linked retinitis pigmentosa (XLRP; RP2 and RP3). We have refined the localization of DXS426 both physically, by mapping it to a deletion which spans the interval Xp21.3-Xp11.23, and genetically, by studying multiply informative crossovers which indicate that DXS426 lies between DXS7 and DXS255 (i.e., Xp11.4-Xp11.22). As this is the region which contains the RP2 gene, RP2 families could be identified on the basis of linkage of XLRP to DXS426. Multiply informative crossovers in two RP2 families indicate that the most likely location of the RP2 gene is between DXS426 and DXS7. DXS426 is therefore an important highly informative marker for the purposes of carrier detection and early diagnosis of RP2 and for the localization of the disease gene.
微卫星标记DXS426定位于Xp21.1 - Xp11.21区间,该染色体区域包含两个X连锁视网膜色素变性(XLRP;RP2和RP3)位点。我们通过将其定位到一个跨越Xp21.3 - Xp11.23区间的缺失区域,从物理角度对DXS426的定位进行了优化;同时通过研究多个信息丰富的交叉,从遗传角度表明DXS426位于DXS7和DXS255之间(即Xp11.4 - Xp11.22)。由于这是包含RP2基因的区域,因此可以基于XLRP与DXS426的连锁关系来鉴定RP2家系。两个RP2家系中多个信息丰富的交叉表明,RP2基因最可能的位置在DXS426和DXS7之间。因此,DXS426对于RP2携带者检测和早期诊断以及疾病基因定位而言,是一个重要的高信息含量标记。