Naveira H, Fontdevila A
Chromosoma. 1985;91(2):87-94. doi: 10.1007/BF00294050.
Introgression of a chromosome segment from Drosophila serido into the genome of its sibling D. buzzatii brought about the release of mutator potential in the hybrids. Mutator activity was determined by examining the frequency of new chromosomal rearrangements, that appeared only in the progeny of hybrid individuals. Mutation frequency was 30 times greater in the progeny of hybrid males than in that of hybrid females. There was a remarkable influence of the D. buzzatii genetic background on the frequency of production of these new rearrangements. The appearance of a new rearrangement did not depend on the genotype of the larva that bore it, but only on that of its hybrid progenitor. Among the new rearrangements there were inversions, translocations, and duplications. The number of translocations was significantly lower than that of inversions or duplications; this last type was the most frequently recorded. The distribution of the aberrations among the four major autosomes seemed to be homogeneous, although the total number of breakpoints was significantly greater in chromosome 4 than in the others. No rearrangement was found on the X chromosome. Breakpoints within three of the four affected autosomes were not randomly distributed.
将果蝇Serido的一个染色体片段渗入其同胞种果蝇Buzzatii的基因组中,导致杂种中诱变潜能的释放。通过检查仅在杂种个体后代中出现的新染色体重排频率来确定诱变活性。杂种雄性后代的突变频率比杂种雌性后代高30倍。果蝇Buzzatii的遗传背景对这些新重排产生频率有显著影响。新重排的出现不取决于携带它的幼虫的基因型,而仅取决于其杂种亲本的基因型。在新重排中,有倒位、易位和重复。易位的数量明显低于倒位或重复的数量;最后这种类型是记录最频繁的。畸变在四条主要常染色体上的分布似乎是均匀的,尽管第4号染色体上的断点总数明显多于其他染色体。在X染色体上未发现重排。四条受影响常染色体中的三条上的断点不是随机分布的。