首页> 外文期刊>Molecular biology and evolution >The frequency distribution of nucleotide variation in Drosophila simulans
【24h】

The frequency distribution of nucleotide variation in Drosophila simulans

机译:拟果蝇核苷酸变异频率分布

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Patterns of codon bias in Drosophila suggest that silent mutations can be classified into two types: unpreferred (slightly deleterious) and preferred (slightly beneficial). Results of previous analyses of polymorphism and divergence in Drosophila simulans were interpreted as supporting a mutation-selection-drift model in which slightly deleterious, silent mutants make significantly greater contributions to polymorphism than to divergence. Frequencies of unpreferred polymorphisms were inferred to be lower than frequencies of other silent polymorphisms. Here, I analyzed additional D. simulans data to reevaluate the support for these ideas. I found that D. simulans has fixed more unpreferred than preferred mutations, suggesting that this lineage has not been at mutation-selection-drift equilibrium at silent sites. Frequencies of polarized unpreferred polymorphisms are not skewed toward rare alleles. However, frequencies of unpolarized unpreferred codons are lower in high-bias genes than in low-bias genes. This supports the idea that unpreferred codons are borderline deleterious mutations. Purifying selection on silent sites appears to be stronger at twofold-degenerate codons than at fourfold-degenerate codons. Finally, I found that X-linked polymorphisms occur at a higher average frequency than polymorphisms on chromosome arm 3R, even though an average X-linked site is significantly less likely to be polymorphic than an average site on 3R. This result supports a previous analysis of D. simulans indicating different population genetics of X-linked versus autosomal mutations.
机译:果蝇的密码子偏倚模式表明,沉默突变可分为两种类型:非首选(轻微有害)和首选(轻微有益)。先前对果蝇模拟多态性和分化的分析结果被解释为支持突变-选择-漂移模型,其中轻微有害的、沉默的突变体对多态性的贡献明显大于对分化的贡献。推断出非首选多态性的频率低于其他沉默多态性的频率。在这里,我分析了更多的模拟蛤蜊数据,以重新评估对这些想法的支持。我发现 D. simulans 修复的非首选突变多于首选突变,这表明该谱系在沉默位点没有处于突变-选择-漂移平衡状态。极化非首选多态性的频率不会偏向于稀有等位基因。然而,高偏倚基因中非极化非首选密码子的频率低于低偏倚基因。这支持了这样一种观点,即非首选密码子是临界有害突变。沉默位点的纯化选择似乎在两重简并密码子上比在四重简并密码子上更强。最后,我发现 X 连锁多态性的平均发生频率高于染色体臂 3R 上的多态性,尽管平均 X 连锁位点的多态性明显低于 3R 上的平均位点。该结果支持先前对拟拟 D. simulans 的分析,表明 X 连锁突变与常染色体突变的群体遗传学不同。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号