Genome-mismatch scanning (GMS) is a new method of linkage analysis that rapidly isolates regions of identity between two genomes. DNA molecules from regions of identity by descent from two relatives are isolated based on their ability to form extended mismatch-free heteroduplexes. We have applied this rapid technology to identify the chromosomal region shared by two fifth-degree cousins with autosomal dominant iridogoniodysgenesis anomaly (IGDA), a rare ocular neurocristopathy. Markers on the short arm of human chromosome 6p were recovered, consistent with the results of conventional linkage analysis conducted in parallel, indicating linkage of IGDA to 6p25. Control markers tested on a second human chromosome were not recovered. A GMS error rate of approximately 11% was observed, well within an acceptable range for a rapid, first screening approach, especially since GMS results would be confirmed by family analysis with selected markers from the putative region of identity by descent. These results demonstrate not only the value of this technique in the rapid mapping of human genetic traits, but the first application of GMS to a multicellular organism.

译文

基因组错配扫描 (GMS) 是一种新的连锁分析方法,可快速分离两个基因组之间的同一性区域。根据两个亲戚的血统从同一性区域分离出DNA分子,这是基于它们形成扩展的无错配异双链体的能力。我们已应用这项快速技术来识别常染色体显性显性虹膜增生异常 (IGDA) (一种罕见的眼部神经病变) 的5分之2度近亲共有的染色体区域。恢复了人类6p染色体短臂上的标记,与并行进行的常规连锁分析的结果一致,表明IGDA与6p25连锁。未恢复在第二条人类染色体上测试的对照标记。观察到大约11% 的GMS错误率,在快速、第一筛选方法的可接受范围内,特别是因为GMS结果将通过家族分析来确认,该家族分析具有来自推定的同一性区域的选定标记通过下降。这些结果不仅证明了该技术在快速绘制人类遗传性状方面的价值,而且证明了GMS在多细胞生物中的首次应用。

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