Creer Simon, Malhotra Anita, Thorpe Roger S, Pook Catharine E
School of Biological Sciences, University of Wales, Bangor, Gwynedd, LL57 2UW, UK.
Cladistics. 2005 Aug;21(4):390-395. doi: 10.1111/j.1096-0031.2005.00072.x.
Nuclear introns are increasingly used as phylogenetic markers. Here, we present a multidisciplinary approach towards optimal locus selection and amplification using Asian pitvipers as an example of a non-model taxon, and raise the profile of length variant heterozygotes (LVHs) in intron loci. Taxon-specific primers were identified using a bioinformatic approach, and also designed from existing exon primed, intron crossing (EPIC) primer amplifications. Eleven further universal EPIC primer pairs were assayed using a range of PCR optimization strategies. Taxon-specific primers yielded the most consistent amplifications, but assaying a large number of universal EPIC primers yielded another appropriate locus for phylogenetic purposes. Modified Taq DNA polymerases such as JumpStart™Taq either significantly improved the specificity and yield of EPIC PCR amplifications (of low copy number nuclear targets), or resulted in amplifications that were not significantly worse than those derived from a generic Taq DNA polymerase. Finally, LVHs were detected in all loci that were sequenced suggesting that they are relatively common in introns. This study provides an efficient and cost effective template for the successful identification of intron markers for molecular systematics which is universally applicable to other non-model taxon groups.
核内含子越来越多地被用作系统发育标记。在此,我们以亚洲蝰蛇这一非模式分类群为例,展示了一种用于最佳基因座选择和扩增的多学科方法,并提高了内含子基因座中长度变异杂合子(LVH)的关注度。通过生物信息学方法鉴定了分类群特异性引物,也从现有的外显子引物介导的内含子交叉(EPIC)引物扩增中进行设计。使用一系列PCR优化策略对另外11对通用EPIC引物对进行了检测。分类群特异性引物产生了最一致的扩增结果,但检测大量通用EPIC引物产生了另一个适用于系统发育目的的基因座。诸如JumpStart™Taq等改良的Taq DNA聚合酶要么显著提高了EPIC PCR扩增(低拷贝数核靶标)的特异性和产量,要么导致扩增结果不比从通用Taq DNA聚合酶获得的结果差很多。最后,在所有测序的基因座中都检测到了LVH,这表明它们在内含子中相对常见。本研究为成功鉴定用于分子系统学的内含子标记提供了一种高效且经济高效的模板,该模板普遍适用于其他非模式分类群。