首页> 美国卫生研究院文献>Genetics >Polymorphism, recombination and alternative unscrambling in the DNA polymerase alpha gene of the ciliate Stylonychia lemnae (Alveolata; class Spirotrichea).
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Polymorphism, recombination and alternative unscrambling in the DNA polymerase alpha gene of the ciliate Stylonychia lemnae (Alveolata; class Spirotrichea).

机译:纤毛针茅兰(DNA)的DNA聚合酶α基因的多态性,重组和替代性解读(Alveolata; Spirotrichea类)。

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摘要

DNA polymerase alpha is the most highly scrambled gene known in stichotrichous ciliates. In its hereditary micronuclear form, it is broken into >40 pieces on two loci at least 3 kb apart. Scrambled genes must be reassembled through developmental DNA rearrangements to yield functioning macronuclear genes, but the mechanism and accuracy of this process are unknown. We describe the first analysis of DNA polymorphism in the macronuclear version of any scrambled gene. Six functional haplotypes obtained from five Eurasian strains of Stylonychia lemnae were highly polymorphic compared to Drosophila genes. Another incompletely unscrambled haplotype was interrupted by frameshift and nonsense mutations but contained more silent mutations than expected by allelic inactivation. In our sample, nucleotide diversity and recombination signals were unexpectedly high within a region encompassing the boundary of the two micronuclear loci. From this and other evidence we infer that both members of a long repeat at the ends of the loci provide alternative substrates for unscrambling in this region. Incongruent genealogies and recombination patterns were also consistent with separation of the two loci by a large genetic distance. Our results suggest that ciliate developmental DNA rearrangements may be more probabilistic and error prone than previously appreciated and constitute a potential source of macronuclear variation. From this perspective we introduce the nonsense-suppression hypothesis for the evolution of ciliate altered genetic codes. We also introduce methods and software to calculate the likelihood of hemizygosity in ciliate haplotype samples and to correct for multiple comparisons in sliding-window analyses of Tajima's D.
机译:DNA聚合酶α是粘虫纤毛中已知的最高度混乱的基因。以其遗传性微核形式,它在两个至少相距3 kb的基因座上被分成40多个片段。必须通过发育性DNA重排重新组装加扰的基因,以产生功能正常的大核基因,但是该过程的机制和准确性尚不清楚。我们描述了任何加扰基因的大核版本中DNA多态性的首次分析。与果蝇基因相比,从五个欧亚甜菜针茅菌株中获得的六个功能单倍型具有高度多态性。另一个不完整的单倍型被移码和无意义的突变打断,但包含的沉默突变比等位基因失活所预期的多。在我们的样本中,核苷酸多样性和重组信号在包含两个微核基因座边界的区域内异常高。从这个和其他证据中,我们推断出在基因座末端的长重复序列的两个成员都提供了在该区域解扰的替代底物。族谱不一致和重组模式也与两个基因座相距较大的遗传距离相一致。我们的结果表明,纤毛虫发育DNA重排可能比以前认识到的概率更高,更容易出错,并且构成了大核变异的潜在来源。从这个角度出发,我们介绍了纤毛虫改变遗传密码进化过程的无意义抑制假设。我们还介绍了计算纤毛单倍型样品中半合子的可能性并校正Tajima D的滑动窗口分析中的多个比较的方法和软件。

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