Nussbaum R L, Lesko J G, Lewis R A, Ledbetter S A, Ledbetter D H
Proc Natl Acad Sci U S A. 1987 Sep;84(18):6521-5. doi: 10.1073/pnas.84.18.6521.
Choroideremia, an X-chromosome linked retinal dystrophy of unknown pathogenesis, causes progressive nightblindness and eventual central blindness in affected males by the third to fourth decade of life. Choroideremia has been mapped to Xq13-21 by tight linkage to restriction fragment length polymorphism loci. We have recently identified two families in which choroideremia is inherited with mental retardation and deafness. In family XL-62, an interstitial deletion in Xq21 is visible by cytogenetic analysis and two linked anonymous DNA markers, DXYS1 and DXS72, are deleted. In the second family, XL-45, an interstitial deletion was suspected on phenotypic grounds but could not be confirmed by high-resolution cytogenetic analysis. We used phenol-enhanced reassociation of 48,XXXX DNA in competition with excess XL-45 DNA to generate a library of cloned DNA enriched for sequences that might be deleted in XL-45. Two of the first 83 sequences characterized from the library were found to be deleted in probands from family XL-45 as well as from family XL-62. Isolation of these sequences proves that XL-45 does contain a submicroscopic deletion and provides a starting point for identifying overlapping genomic sequences that span the XL-45 deletion. Each overlapping sequence will be studied to identify exons from the choroideremia locus.
无脉络膜症是一种病因不明的X染色体连锁视网膜营养不良症,会导致患病男性在30到40岁时逐渐出现夜盲,并最终导致中央视力失明。通过与限制性片段长度多态性位点紧密连锁,无脉络膜症基因已被定位到Xq13 - 21。我们最近发现了两个家族,其中无脉络膜症与智力迟钝和耳聋一起遗传。在XL - 62家族中,通过细胞遗传学分析可见Xq21的间质性缺失,并且两个连锁的匿名DNA标记DXYS1和DXS72被缺失。在第二个家族XL - 45中,基于表型推测存在间质性缺失,但高分辨率细胞遗传学分析未能证实。我们使用苯酚增强的48,XXXX DNA重结合并与过量的XL - 45 DNA竞争,以生成一个克隆DNA文库,该文库富含可能在XL - 45中缺失的序列。从该文库中鉴定的前83个序列中的两个被发现在XL - 45家族以及XL - 62家族的先证者中缺失。这些序列的分离证明XL - 45确实包含一个亚显微缺失,并为鉴定跨越XL - 45缺失的重叠基因组序列提供了一个起点。将对每个重叠序列进行研究,以鉴定无脉络膜症基因座的外显子。