Freije D, Schlessinger D
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110.
Am J Hum Genet. 1992 Jul;51(1):66-80.
Two yeast artificial chromosome (YAC) libraries were screened for probes in Xq28, around the gene for coagulation factor VIII (F8). A set of 30 YACs were recovered and assembled into a contig spanning at least 1.6 Mb from the DXYS64 locus to the glucose 6-phosphate dehydrogenase gene (G6PD). Overlaps among the YACs were determined by several fingerprinting techniques and by additional probes generated from YAC inserts by using Alu-vector or ligation-mediated PCR. Analysis of more than 30 probes and sequence-tagged sites (STSs) made from the region revealed the presence of several homologous genomic segments. For example, a probe for the DXYS64 locus, which maps less than 500 kb 5' of F8, detects a similar but not identical locus between F8 and G6PD. Also, a probe for the DXS115 locus detects at least three identical copies in this region, one in intron 22 of F8 and at least two more, which are upstream of the 5' end of the gene. Comparisons of genomic and YAC DNA suggest that the multiple loci are not created artifactually during cloning but reflect the structure of uncloned human DNA. On the basis of these data, the most likely order for the loci analyzed is tel-DXYS61-DXYS64-(DXS115-3-DXS115-2)-5'F8-(D XS115-1)-3'F8-G6PD.
对两个酵母人工染色体(YAC)文库进行筛选,以寻找位于凝血因子VIII(F8)基因附近的Xq28区域中的探针。回收了一组30个YAC,并将其组装成一个重叠群,该重叠群从DXYS64位点延伸至葡萄糖6 - 磷酸脱氢酶基因(G6PD),跨度至少为1.6 Mb。通过几种指纹图谱技术以及使用Alu - 载体或连接介导的PCR从YAC插入片段产生的额外探针来确定YAC之间的重叠情况。对该区域产生的30多个探针和序列标签位点(STS)进行分析,发现存在几个同源基因组片段。例如,位于F8基因5'端不到500 kb处的DXYS64位点的一个探针,在F8和G6PD之间检测到一个相似但不完全相同的位点。此外,DXS115位点的一个探针在该区域检测到至少三个相同的拷贝,一个在F8基因的内含子22中,另外至少两个在该基因5'端上游。基因组DNA与YAC DNA的比较表明,多个位点不是在克隆过程中人为产生的,而是反映了未克隆的人类DNA的结构。根据这些数据,所分析位点最可能的顺序是端粒 - DXYS61 - DXYS64 - (DXS115 - 3 - DXS115 - 2) - 5'F8 - (DXS115 - 1) - 3'F8 - G6PD。