首页> 美国卫生研究院文献>Genetics >Negative Segregation Distortion in the Sd System of Drosophila Melanogaster: A Challenge to the Concept of Differential Sensitivity of Rsp Alleles
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Negative Segregation Distortion in the Sd System of Drosophila Melanogaster: A Challenge to the Concept of Differential Sensitivity of Rsp Alleles

机译:果蝇Sd系统中的负偏析畸变:对Rsp等位基因差异敏感性概念的挑战

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摘要

Current models of segregation distortion based on previous experimental results predict that, in the Sd heterozygous Rsp(i)/Rsp(s) male, the chromosome carrying the sensitive Rsp(s) allele is distorted or transmitted in a frequency smaller than that of the expected Mendelian 0.5 relative to the chromosome carrying the insensitive Rsp(i) allele. The present study presents a case where this does not occur, that is, when the genotype of the males is supp-X(SD)/Y; Sd E(SD)Rsp(i) M(SD)(+)/Sd(+) E(SD)(+) Rsp(s) M(SD)(+) where supp-X(SD) is an X chromosome carrying a strong suppressor or suppressors of SD activity and SD(+) E(SD)(+) Rsp(s) M(SD)(+) is the standard cn bw chromosome. Following the ``inseminated female transfer'' procedure, young males of the above genotype carrying the standard-X instead of the supp-X(SD) chromosome show k values for the SD chromosome (frequencies of the SD chromosome recovered among progeny) of about 0.75, but with the supp-X(SD) chromosome, the k values are reduced to 0.36-0.41. Several possibilities other than the mechanism of segregation distortion to explain the reduced k values are ruled out. The occurrence of ``negative segregation distortion'' is clearly demonstrated, where the chromosome carrying the Rsp(i) allele is distorted, but the chromosome with the Rsp(s) allele is not. This result requires a major modification of the current models or even a new model for the mechanism of segregation distortion to accommodate Rsp allele sensitivity or insensitivity. The present study also shows that males of the genotype, Sd Rsp(ss) M(SD)(+)/Sd(+) Rsp(ss) M(SD), are almost completely sterile, but their fertility is considerably increased when SD activity is suppressed by the presence of the supp-X(SD) chromosome. This result suggests that the amount of the Sd product is not limited with respect to the interacting sites available, that is, the amount is large enough to interact with both of the Rsp(ss) alleles.
机译:当前基于先前实验结果的偏析畸变模型预测,在Sd杂合子Rsp(i)/ Rsp(s)雄性中,携带敏感Rsp(s)等位基因的染色体会以比染色体Rsp(i)/ Rsp(s)等位基因小的频率扭曲或传播。相对于携带不敏感Rsp(i)等位基因的染色体的预期孟德尔0.5。本研究提出了一种情况,这种情况不会发生,即,当男性的基因型是supp-X(SD)/ Y时; Sd E(SD)Rsp(i)M(SD)(+)/ Sd(+)E(SD)(+)Rsp(s)M(SD)(+),其中supp-X(SD)是X染色体携带强力抑制或抑制SD活性和SD(+)E(SD)(+)Rsp(s)M(SD)(+)是标准的cn bw染色体。按照``授精雌性转移''程序,携带标准X而不是supp-X(SD)染色体的上述基因型的年轻雄性显示出SD染色体的k值(子代中回收的SD染色体频率)。大约0.75,但使用supp-X(SD)染色体,k值降低到0.36-0.41。排除了除偏析失真机制以外的几种可能性来解释减小的k值。清楚地证明了``负偏析畸变''的发生,其中带有Rsp(i)等位基因的染色体发生了畸变,而带有Rsp(s)等位基因的染色体却没有发生畸变。该结果需要对当前模型进行重大修改,甚至需要针对分离失真机制的新模型,以适应Rsp等位基因的敏感性或敏感性。本研究还表明,基因型为Sd Rsp(ss)M(SD)(+)/ Sd(+)Rsp(ss)M(SD)的雄性几乎完全不育,但当SD时,其生育力大大提高supp-X(SD)染色体的存在抑制了细胞的活性。该结果表明,相对于可用的相互作用位点,Sd产物的量不受限制,即,该量足够大以与两个Rsp(ss)等位基因相互作用。

著录项

  • 期刊名称 Genetics
  • 作者

    Y. Hiraizumi;

  • 作者单位
  • 年(卷),期 1990(125),3
  • 年度 1990
  • 页码 515–525
  • 总页数 11
  • 原文格式 PDF
  • 正文语种
  • 中图分类 遗传学;
  • 关键词

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