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首页> 外文期刊>Genome Biology and Evolution >Validation of Rearrangement Break Points Identified by Paired-End Sequencing in Natural Populations of Drosophila melanogaster
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Validation of Rearrangement Break Points Identified by Paired-End Sequencing in Natural Populations of Drosophila melanogaster

机译:果蝇自然种群中通过配对末端测序确定的重排断裂点的验证

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Several recent studies have focused on the evolution of recently duplicated genes in Drosophila. Currently, however, little is known about the evolutionary forces acting upon duplications that are segregating in natural populations. We used a high-throughput, paired-end sequencing platform (Illumina) to identify structural variants in a population sample of African D. melanogaster. Polymerase chain reaction and sequencing confirmation of duplications detected by multiple, independent paired-ends showed that paired-end sequencing reliably uncovered the break points of structural rearrangements and allowed us to identify a number of tandem duplications segregating within a natural population. Our confirmation experiments show that rates of confirmation are very high, even at modest coverage. Our results also compare well with previous studies using microarrays (Emerson J, Cardoso-Moreira M, Borevitz JO, Long M. 2008. Natural selection shapes genome wide patterns of copy-number polymorphism in Drosophila melanogaster. Science. 320:1629–1631. and Dopman EB, Hartl DL. 2007. A portrait of copy-number polymorphism in Drosophila melanogaster. Proc Natl Acad Sci U S A. 104:19920–19925.), which both gives us confidence in the results of this study as well as confirms previous microarray results. We were also able to identify whole-gene duplications, such as a novel duplication of Or22a, an olfactory receptor, and identify copy-number differences in genes previously known to be under positive selection, like Cyp6g1, which confers resistance to dichlorodiphenyltrichloroethane. Several “hot spots” of duplications were detected in this study, which indicate that particular regions of the genome may be more prone to generating duplications. Finally, population frequency analysis of confirmed events also showed an excess of rare variants in our population, which indicates that duplications segregating in the population may be deleterious and ultimately destined to be lost from the population.
机译:最近的一些研究集中在果蝇中最近重复的基因的进化。但是,目前对于在自然种群中隔离的重复作用的进化力知之甚少。我们使用了高通量,双末端测序平台(Illumina)来鉴定非洲黑腹果蝇种群样本中的结构变异。聚合酶链反应和由多个独立的配对末端检测到的重复序列的测序确认表明,配对末端测序可靠地揭示了结构重排的断裂点,并使我们能够鉴定出在自然种群中分离的许多串联重复序列。我们的确认实验表明,即使覆盖率适中,确认率也很高。我们的结果也与以前使用微阵列的研究进行了比较(Emerson J,Cardoso-Moreira M,Borevitz JO,Long M.2008。自然选择塑造了果蝇果蝇的拷贝数多态性的全基因组模式。Science。320:1629–1631。 and Dopman EB,Hartl DL。2007. Drosophila melanogaster中的拷贝数多态性画像(Proc Natl Acad Sci US A. 104:19920–19925。),这都使我们对这项研究的结果充满信心并得到证实先前的芯片结果。我们还能够鉴定全基因重复,例如嗅觉受体Or22a的新重复,并鉴定先前已知处于正选择状态的基因(例如赋予对二氯二苯基三氯乙烷的抗性的Cyp6g1)的拷贝数差异。在这项研究中检测到几个重复的“热点”,这表明基因组的特定区域可能更容易产生重复。最后,对确诊事件的人群频率分析还显示,在我们的人群中存在过多的稀有变异,这表明在人群中隔离的重复项可能是有害的,最终注定会从人群中消失。

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