Black D M, Jackson M S, Kidwell M G, Dover G A
Department of Genetics, University of Cambridge, UK.
EMBO J. 1987 Dec 20;6(13):4125-35. doi: 10.1002/j.1460-2075.1987.tb02758.x.
Molecular and genetic analysis has revealed a specific P factor deletion derivative (the KP element) which is able to repress P-induced hybrid dysgenesis. All naturally occurring strains lacking the P cytotype (M') that were examined, throughout the world contain up to 30 copies of KP per haploid genome together with complete P factors. The KP element is derived from the P factor by an internal deletion of 1753 bp removing nucleotides 808-2560 and is transcribed to yield an abundant 0.8-kb poly(A)+ RNA with the coding capacity for an in-frame 207 amino acid polypeptide. Genetic crosses show that KP elements preferentially accumulate in the presence of P factors and suppress hybrid dysgenesis. Suppression is transmitted through both sexes and is thus distinct from the maternally transmitted P cytotype mode of suppression. The spread of KP elements is probably due to the continual selection of individuals with the highest numbers of KP elements in which P-induced hybrid dysgenesis is suppressed.
分子和遗传学分析揭示了一种特定的P因子缺失衍生物(KP元件),它能够抑制P诱导的杂种不育。在世界各地检查的所有缺乏P细胞型(M')的自然发生菌株中,每个单倍体基因组含有多达30个KP拷贝以及完整的P因子。KP元件是由P因子通过内部缺失1753 bp(去除核苷酸808 - 2560)衍生而来,转录后产生丰富的0.8 kb聚腺苷酸化(poly(A)+)RNA,其编码能力为一个读码框内的207个氨基酸的多肽。遗传杂交表明,KP元件在P因子存在的情况下优先积累并抑制杂种不育。抑制作用通过两性传递,因此不同于母系传递的P细胞型抑制模式。KP元件的传播可能是由于对具有最高数量KP元件且P诱导的杂种不育被抑制的个体进行持续选择的结果。