Simmler M C, Rouyer F, Vergnaud G, Nyström-Lahti M, Ngo K Y, de la Chapelle A, Weissenbach J
Nature. 1985;317(6039):692-7. doi: 10.1038/317692a0.
A DNA probe from a human Y chromosome-derived cosmid detects a single-copy genomic DNA fragment which can appear in different allelic forms shared by both sex chromosomes. Variants at this DNA locus show an autosomal pattern of inheritance, undergo recombination with sexual phenotype and can therefore be described as 'pseudoautosomal'. Another probe from the same cosmid detects a sequence repeated 15-20 times per haploid genome. These repeats also appear pseudoautosomal and map exclusively to the short-arm terminal region of each sex chromosome.
来自人类Y染色体衍生黏粒的DNA探针检测到一个单拷贝基因组DNA片段,该片段可呈现出由两条性染色体共享的不同等位基因形式。此DNA位点的变异显示出常染色体遗传模式,与性表型发生重组,因此可被描述为“假常染色体的”。来自同一黏粒的另一个探针检测到一个在每个单倍体基因组中重复15 - 20次的序列。这些重复序列也呈现假常染色体特征,并且专门定位于每条性染色体的短臂末端区域。