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The genetics and evolution of the Winters sex-ratio in Drosophila.

机译:果蝇温特性别比的遗传和进化。

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摘要

Sex chromosome meiotic drive elements are selfish genes that increase in frequency in populations due to their transmission ratio advantage, causing skews in population sex ratios. Suppressors of drivers are strongly selected to restore Fisherian sex ratios. We characterize the structure, function, and evolution of an X-linked sex ratio distorter in Drosophila called the Winters sex-ratio which evolved in the ancestor of D. simulans, D. mauritiana, and D. sechellia between 2.3 million and 250,000 years ago. Distortion is caused by Distorter on the X (Dox), a gene that was created through the duplication of Mother of Dox (MDox), which is 70 kilo bases distal to Dox. Dox causes skewed progeny sex ratios by disrupting the development of Y-bearing sperm through abnormal chromosome condensation and nuclear elongation. A dominant suppressor gene, Not Much Yang (Nmy) evolved on chromosome 3R as a retrotransposed copy of Dox.;We collect molecular population genetic data from D. simulans and D. mauritiana, sister species who diverged 250,000 years ago. Through structural analysis of gene regions, we show that Dox and MDox have a single origin and that each arose through non-allelic homologous recombination, mediated by 360bp satellite DNA repeat elements that flank the genes. D. simulans is polymorphic for all three genes whereas D. mauritiana has fixed MDox and Nmy, but is polymorphic for Dox. Coalescent modeling of positive selection indicates that selective sweeps have occurred at all three genes in North American populations of D. simulans in the last 100,000 years. In addition, the derived alleles in D. simulans show reduced diversity relative to ancestral null loci, which lack the gene insertions. Phylogenetic analysis is consistent with recurrent selective sweeps at Dox and Nmy in D. simulans. The high frequency of Nmy in natural populations of D. simulans likely silences Dox, and the gene has accumulated loss-of-function mutations. In contrast, Dox and MDox remain completely undifferentiated from each other in D. mauritiana, indicating that Dox has not been neo- or sub-functionalized and may be eventually lost due to genetic drift.
机译:性染色体减数分裂驱动因子是自私的基因,由于其传播比率优势而在人群中频率增加,从而导致人群性别比率出现偏差。强烈选择司机抑制器以恢复渔夫的性别比例。我们表征了果蝇中X连锁性别比率畸变者的结构,功能和进化,这种现象称为温特斯性别比,它在D. simulans,D。mauritiana和D. sechellia的祖先之间进化了230万到250,000年前。扭曲是由X(Dox)上的Distorter引起的,该基因是通过复制Dox妈妈(MDox)而产生的,该基因位于Dox的远端70千克碱基处。 Dox通过异常的染色体凝缩和核伸长来破坏含Y精子的发育,从而导致后代性别比例出现偏差。显性抑制基因Not Much Yang(Nmy)在染色体3R上作为Dox的转座复制品进化。我们收集了25万年前发散的姊妹物种D. simulans和D. mauritiana的分子种群遗传数据。通过对基因区域的结构分析,我们显示Dox和MDox具有单一起源,并且各自通过非等位基因同源重组而产生,该重组由位于基因两侧的360bp卫星DNA重复元件介导。 D. simulans对所有三个基因都是多态的,而D. mauritiana具有固定的MDox和Nmy,但对Dox是多态的。正选择的合并模型表明,在过去的100,000年中,北美模拟猿种群中的所有三个基因均发生了选择性扫描。另外,相对于没有基因插入的祖先无效基因座,拟杆菌中的衍生等位基因显示出降低的多样性。系统发育分析与D. simulans中Dox和Nmy的周期性选择性扫描一致。 N. simulans自然种群中Nmy的高频率可能会使Dox沉默,并且该基因积累了功能丧失突变。相反,在D. mauritiana中,Dox和MDox仍然彼此完全未分化,这表明Dox尚未被新功能或亚功能化,并可能由于遗传漂移而最终丢失。

著录项

  • 作者

    Kingan, Sarah Bowman.;

  • 作者单位

    Harvard University.;

  • 授予单位 Harvard University.;
  • 学科 Biology Molecular.;Biology Zoology.;Biology Genetics.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 134 p.
  • 总页数 134
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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