Nitasaka E, Yamazaki T
Department of Biology, Faculty of Science, Kyushu University, Fukuoka.
Jpn J Genet. 1988 Aug;63(4):303-12. doi: 10.1266/jjg.63.303.
The X-linked singed locus is concerned with the bristle phenotype and female sterility, and is known as a hot spot of P element insertion. A moderate allele of singed, singed-weak (snw) (Engels, 1979; 1984) is inserted with P elements. It is used as an index of P element activity, since it mutates at a high frequency to either a more extreme allele, singed-extreme (sne), or to a phenotype that is equivalent to the wild type (sn+) when an autonomous P element exists. We show here that snw is inserted with two defective P elements in reverse orientation, and the two alternate mutational events (sn+ and sne) are caused by the excision of one or the other of the P elements present in the singed gene. It is interesting that sn+ and sne are inserted with a single P element in the same position, but show very different phenotypes. The insertional sites of P elements in the singed locus possibly contain an unidentified repetitive sequence, which is repeated dozens of times per haploid genome of the wild-type strain Canton-S.
X 连锁的“焦刚毛”基因座与刚毛表型和雌性不育有关,并且是 P 因子插入的热点区域。“焦刚毛”的一个中度等位基因,即弱焦刚毛(snw)(恩格斯,1979 年;1984 年)被 P 因子插入。它被用作 P 因子活性的指标,因为当存在自主 P 因子时,它会高频突变为更极端的等位基因,即极端焦刚毛(sne),或者突变为等同于野生型(sn+)的表型。我们在此表明,snw 被两个反向的缺陷型 P 因子插入,并且这两个交替的突变事件(sn+和 sne)是由“焦刚毛”基因中存在的一个或另一个 P 因子的切除引起的。有趣的是,sn+和 sne 在同一位置被单个 P 因子插入,但表现出非常不同的表型。P 因子在“焦刚毛”基因座中的插入位点可能包含一个未鉴定的重复序列,该序列在野生型品系 Canton-S 的每个单倍体基因组中重复数十次。