ARC Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, QLD 4811, Australia.
Harvey Mudd College, Biology Department, 1250 N. Dartmouth Ave., Claremont, CA 91711, USA; Department of Invertebrate Zoology, National Museum of Natural History, Smithsonian Institution, Washington DC 20560, USA.
Mol Phylogenet Evol. 2020 Dec;153:106944. doi: 10.1016/j.ympev.2020.106944. Epub 2020 Aug 27.
Targeted enrichment of genomic DNA can profoundly increase the phylogenetic resolution of clades and inform taxonomy. Here, we redesign a custom bait set previously developed for the cnidarian class Anthozoa to more efficiently target and capture ultraconserved elements (UCEs) and exonic loci within the subclass Hexacorallia. We test this enhanced bait set (targeting 2476 loci) on 99 specimens of scleractinian corals spanning both the "complex" (Acroporidae, Agariciidae) and "robust" (Fungiidae) clades. Focused sampling in the staghorn corals (genus Acropora) highlights the ability of sequence capture to inform the taxonomy of a clade previously deficient in molecular resolution. A mean of 1850 (±298) loci were captured per taxon (955 UCEs, 894 exons), and a 75% complete concatenated alignment of 96 samples included 1792 loci (991 UCE, 801 exons) and ~1.87 million base pairs. Maximum likelihood and Bayesian analyses recovered robust molecular relationships and revealed that species-level relationships within the Acropora are incongruent with traditional morphological groupings. Both UCE and exon datasets delineated six well-supported clades within Acropora. The enhanced bait set will facilitate investigations of the evolutionary history of many important groups of reef corals, particularly where previous molecular marker development has been unsuccessful.
靶向富集基因组 DNA 可以极大地提高进化枝的系统发育分辨率,并为分类学提供信息。在这里,我们重新设计了以前为腔肠动物门珊瑚纲开发的定制诱饵集,以更有效地靶向和捕获超保守元件 (UCE) 和子类六放珊瑚亚纲内的外显子基因座。我们在 99 个石珊瑚标本上测试了这个增强的诱饵集(靶向 2476 个基因座),这些标本涵盖了“复杂”(鹿角珊瑚科、扇珊瑚科)和“强壮”(真菌珊瑚科)两个分支。在鹿角珊瑚属(Acropora)的重点采样突出了序列捕获能够为一个以前在分子分辨率上不足的分支的分类学提供信息的能力。每个分类群平均捕获了 1850(±298)个基因座(955 个 UCE,894 个外显子),96 个样本的 75%完整串联比对包含 1792 个基因座(991 个 UCE,801 个外显子)和约 187 万碱基对。最大似然和贝叶斯分析恢复了稳健的分子关系,并表明鹿角珊瑚属内的种间关系与传统的形态分组不一致。UCE 和外显子数据集都将鹿角珊瑚属划分为六个支持良好的分支。增强的诱饵集将促进对许多重要珊瑚礁群体的进化历史的研究,特别是在以前的分子标记开发不成功的情况下。