Winzeler E A, Richards D R, Conway A R, Goldstein A L, Kalman S, McCullough M J, McCusker J H, Stevens D A, Wodicka L, Lockhart D J, Davis R W
Department of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305-5307, USA.
Science. 1998 Aug 21;281(5380):1194-7. doi: 10.1126/science.281.5380.1194.
As more genomes are sequenced, the identification and characterization of the causes of heritable variation within a species will be increasingly important. It is demonstrated that allelic variation in any two isolates of a species can be scanned, mapped, and scored directly and efficiently without allele-specific polymerase chain reaction, without creating new strains or constructs, and without knowing the specific nature of the variation. A total of 3714 biallelic markers, spaced about every 3.5 kilobases, were identified by analyzing the patterns obtained when total genomic DNA from two different strains of yeast was hybridized to high-density oligonucleotide arrays. The markers were then used to simultaneously map a multidrug-resistance locus and four other loci with high resolution (11 to 64 kilobases).
随着越来越多的基因组被测序,识别和表征物种内可遗传变异的原因将变得越来越重要。结果表明,无需等位基因特异性聚合酶链反应、无需创建新菌株或构建体、也无需了解变异的具体性质,就可以直接且高效地扫描、定位和评分一个物种任意两个分离株中的等位基因变异。通过分析来自两种不同酵母菌株的总基因组DNA与高密度寡核苷酸阵列杂交时获得的模式,共鉴定出3714个双等位基因标记,这些标记大约每隔3.5千碱基分布一个。然后利用这些标记对一个多药抗性位点和其他四个位点进行了高分辨率(11至64千碱基)的同时定位。