Vetrie D, Bobrow M, Harris A
Paediatric Research Unit, United Medical School, Guy's Hospital, London, United Kingdom.
Genomics. 1993 Mar;15(3):631-42. doi: 10.1006/geno.1993.1118.
Several genes involved in human genetic diseases map to the Xq22 band on the long arm of the human X chromosome. We have constructed a long-range restriction map of the most proximal part of Xq22. Initially, pulsed-field gel electrophoresis, in combination with rare-cutting restriction enzymes, was used to try and establish physical linkage of 11 polymorphic and nonpolymorphic DNA markers. This approach resulted in the construction of three long-range restriction maps around groups of physically linked Xq22 markers that spanned over 5.0 Mb of DNA. Yeast artificial chromosome clones were used to organize the three long-range maps onto a contiguous 5.2-Mb stretch of Xq22. The order of markers in this region was shown to be cen-GLA-DXS178-DXS101-DXS83-DXS24-DXS101-+ ++DXS54-PLP-DXS94-DXS147-DXS17-DXS87-tel . The results of this study suggest that the proximal part of Xq22 may be rich in genes. Construction of a physical map for this region will, therefore, facilitate the localization and subsequent isolation of novel genes.
几个与人类遗传疾病相关的基因定位到人类X染色体长臂的Xq22带。我们构建了Xq22最近端部分的长程限制酶切图谱。最初,脉冲场凝胶电泳结合稀有切割限制酶,用于尝试建立11个多态性和非多态性DNA标记的物理连锁。这种方法导致围绕跨越超过5.0 Mb DNA的物理连锁Xq22标记组构建了三个长程限制酶切图谱。酵母人工染色体克隆用于将这三个长程图谱整理到Xq22的一个连续5.2-Mb片段上。该区域标记的顺序显示为cen-GLA-DXS178-DXS101-DXS83-DXS24-DXS101- +++DXS54-PLP-DXS94-DXS147-DXS17-DXS87-端粒。这项研究的结果表明Xq22的近端部分可能富含基因。因此,构建该区域的物理图谱将有助于新基因的定位和后续分离。