Laboratory of Genetics, University of Wisconsin, Madison, Wisconsin 53706.
Genetics. 1983 Apr;103(4):659-73. doi: 10.1093/genetics/103.4.659.
Segregation distorter (SD) chromosomes are preferentially transmitted to offspring from heterozygous SD/SD(+) males owing to the induced dysfunction of the SD(+)-bearing sperm. This phenomenon involves at least two major loci: the Sd locus whose presence is necessary for distortion to occur and the Rsp locus which acts as the site of Sd action. Several additional loci on SD chromosomes enhance distortion.-In a previous study deletions were used to map the Sd locus and to determine some of its properties. We have extended this analysis with the isolation and characterization of 14 new deletions in the Sd region. From our results we conclude (1) SD chromosomes contain a single Sd locus located in region 37D2-6 of the salivary gland chromosome map. Deletion of this locus in any of three SD chromosomes now studied results in complete loss of ability to distort a sensitive chromosome; (2) the reduced male fecundity observed in many homozygous SD or SD(i)/SD(j) combinations is due at least in part to the action of the Sd locus. The fecundity of these males can be substantially increased by deletion of one Sd locus. Thus, it is the presence of two doses of Sd rather than the absence of Sd(+) that produces the lowered male fecundity in SD homozygotes; (3) Sd behaves as a neomorph, whereas Sd(+), if it exists at all, is amorphic with respect to segregation distortion; (4) these results support a model in which the Sd product is made in limiting amounts and the interaction of this product with the Rsp locus causes sperm dysfunction. The Sd product appears to act preferentially at Rsp(s) (sensitive-Responder) but may also act at Rsp(i) (insensitive-Responder).
分离歪曲器 (SD) 染色体由于携带 SD(+) 的精子功能失调,优先传递给杂合 SD/SD(+) 雄性的后代。这种现象至少涉及两个主要基因座:Sd 基因座,其存在是发生扭曲的必要条件,以及 Rsp 基因座,它作为 Sd 作用的位点。SD 染色体上的几个其他基因座增强了扭曲。-在之前的研究中,我们使用缺失来定位 Sd 基因座并确定其一些特性。我们通过分离和鉴定 Sd 区域的 14 个新缺失来扩展了这一分析。从我们的结果中,我们得出结论:(1) SD 染色体包含一个位于唾腺染色体图谱 37D2-6 区的单一 Sd 基因座。在现在研究的三个 SD 染色体中的任何一个中缺失这个基因座,都会导致完全丧失扭曲敏感染色体的能力;(2) 在许多纯合 SD 或 SD(i)/SD(j) 组合中观察到的雄性生育力降低至少部分是由于 Sd 基因座的作用。这些雄性的生育力可以通过缺失一个 Sd 基因座而大大提高。因此,是两个剂量的 Sd 的存在而不是 Sd(+) 的缺失导致 SD 纯合子中的雄性生育力降低;(3) Sd 表现为一个新形态,而 Sd(+),如果存在的话,在分离扭曲方面是无形态的;(4) 这些结果支持了这样一种模型,即 Sd 产物以有限的量产生,并且该产物与 Rsp 基因座的相互作用导致精子功能失调。Sd 产物似乎优先作用于 Rsp(s)(敏感-应答者),但也可能作用于 Rsp(i)(不敏感-应答者)。