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Challenges and pitfalls in the characterization of anonymous outlier AFLP markers in non-model species: lessons from an ocellated lizard genome scan

机译:非模型物种中匿名离群值AFLP标记的表征面临的挑战和陷阱:来自有孔蜥蜴基因组扫描的教训

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摘要

In the last few years, dozens of studies have documented the detection of loci influenced by selection from genome scans in a wide range of non-model species. Many of those studies used amplified fragment length polymorphism (AFLP) markers, which became popular for being easily applicable to any organism. However, because they are anonymous markers, AFLPs impose many challenges for their isolation and identification. Most recent AFLP genome scans used capillary electrophoresis (CE), which adds even more obstacles to the isolation of bands with a specific size for sequencing. These caveats might explain the extremely low number of studies that moved from the detection of outlier AFLP markers to their actual isolation and characterization. We document our efforts to characterize a set of outlier AFLP markers from a previous genome scan with CE in ocellated lizards (Lacerta lepida). Seven outliers were successfully isolated, cloned and sequenced. Their sequences are noncoding and show internal indels or polymorphic repetitive elements (microsatellites). Three outliers were converted into codominant markers by using specific internal primers to sequence and screen population variability from undigested DNA. Amplification in closely related lizard species was also achieved, revealing remarkable interspecific conservation in outlier loci sequences. We stress the importance of following up AFLP genome scans to validate selection signatures of outlier loci, but also report the main challenges and pitfalls that may be faced during the process.
机译:在过去的几年中,数十项研究记录了在各种非模型物种中,受基因组扫描选择影响的基因座检测。这些研究中的许多研究都使用了扩增的片段长度多态性(AFLP)标记,由于易于应用于任何生物而广受欢迎。但是,由于AFLP是匿名标记,因此AFLP对其隔离和识别提出了许多挑战。最近的AFLP基因组扫描使用毛细管电泳(CE),这为分离具有特定大小的测序带增加了更多障碍。这些警告可能解释了从异常的AFLP标记的检测到其实际隔离和表征的研究数量极少。我们记录了我们的工作,以表征从先前的基因组扫描中,有色蜥蜴(Lacerta lepida)具有CE的异常基因组AFLP标记。成功分离,克隆和测序了七个异常值。它们的序列是非编码的,并显示内部插入缺失或多态性重复元件(微卫星)。通过使用特异的内部引物对未消化的DNA进行测序和筛选群体变异性,将三个异常值转化为显性标记。还实现了密切相关的蜥蜴物种的扩增,揭示了异常基因座序列中的显着种间保守性。我们强调跟踪AFLP基因组扫描以验证异常基因座的选择特征的重要性,而且还报告了在此过程中可能面临的主要挑战和陷阱。

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