4.7 Article

An enhanced target-enrichment bait set for Hexacorallia provides phylogenomic resolution of the staghorn corals (Acroporidae) and close relatives

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ympev.2020.106944

关键词

Scleractinia; Targeted enrichment; Ultraconserved elements; UCEs; Exon; Phylogenetics

资金

  1. ARC DECRA Fellowships [DE170100516, DE180100746]
  2. ARC Centre of Excellence Programme [CE140100020]
  3. NSF-DEB [1457817]
  4. Direct For Biological Sciences
  5. Division Of Environmental Biology [1457817] Funding Source: National Science Foundation
  6. Australian Research Council [DE180100746, DE170100516] Funding Source: Australian Research Council

向作者/读者索取更多资源

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 Glade 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 similar to 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.

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