Kidwell M G, Kidwell J F
J Hered. 1975 Nov-Dec;66(6):367-75. doi: 10.1093/oxfordjournals.jhered.a108649.
Spontaneous male recombination and visible mutations were observed in second and third chromosomes derived from an isogenic line, ID, previously found to exhibit a high recessive lethal mutation rate. All three types of events tend to occur very early in spermatogenesis resulting in large clusters of identical recombinant or mutant progeny from a single male. Mutations and male recombination exchange points tend to be located more frequently in the right arm than in the left in both second and third chromosomes but for a trivial reason in the case of chromosome 2. No significant differences in male or female recombination were found between the progeny of reciprocal crosses. Male recombination in chromosome 2, like recessive lethal mutation, is independent of the presence of ID third chromosomes in the same genome. Both quantitative and qualitative differences in male recombination were found when ID chromosomes were compared with others extracted from natural populations.
在源自近交系ID的第二和第三条染色体中观察到自发雄性重组和可见突变,该近交系ID先前被发现具有较高的隐性致死突变率。所有这三种类型的事件往往在精子发生的早期就会发生,从而导致来自单个雄性的大量相同重组或突变后代的聚集。在第二和第三条染色体中,突变和雄性重组交换点往往更频繁地位于右臂而非左臂,但就第二条染色体而言,原因微不足道。正反交后代之间在雄性或雌性重组方面未发现显著差异。第二条染色体中的雄性重组,与隐性致死突变一样,与同一基因组中ID第三条染色体的存在无关。当将ID染色体与从自然种群中提取的其他染色体进行比较时,发现雄性重组在数量和质量上都存在差异。