Hidden diversity of Ctenophora revealed by new mitochondrial COI primers and sequences

被引:14
作者
Christianson, Lynne M. [1 ]
Johnson, Shannon B. [1 ]
Schultz, Darrin T. [1 ,2 ]
Haddock, Steven H. D. [1 ]
机构
[1] Monterey Bay Aquarium Res Inst, Moss Landing, CA 95039 USA
[2] Univ Calif Santa Cruz, Dept Biomol Engn & Bioinformat, Santa Cruz, CA 95064 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
barcoding; biodiversity; Ctenophora; cytochrome-c oxidase; eDNA; metabarcoding; primers; OXIDASE SUBUNIT-I; DNA; EVOLUTION; SPONGES; GENOME; MODEL;
D O I
10.1111/1755-0998.13459
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mitochondrial gene cytochrome-c-oxidase subunit 1 (COI) is useful in many taxa for phylogenetics, population genetics, metabarcoding, and rapid species identifications. However, the phylum Ctenophora (comb jellies) has historically been difficult to study due to divergent mitochondrial sequences and the corresponding inability to amplify COI with degenerate and standard COI "barcoding" primers. As a result, there are very few COI sequences available for ctenophores, despite over 200 described species in the phylum. Here, we designed new primers and amplified the COI fragment from members of all major groups of ctenophores, including many undescribed species. Phylogenetic analyses of the resulting COI sequences revealed high diversity within many groups that was not evident from more conserved 18S rDNA sequences, in particular among the Lobata (Ctenophora; Tentaculata; Lobata). The COI phylogenetic results also revealed unexpected community structure within the genus Bolinopsis, suggested new species within the genus Bathocyroe, and supported the ecological and morphological differences of some species such as Lampocteis cruentiventer and similar undescribed lobates (Lampocteis sp. "V" stratified by depth, and "A" differentiated by colour). The newly designed primers reported herein provide important tools to enable researchers to illuminate the diversity of ctenophores worldwide via quick molecular identifications, improve the ability to analyse environmental DNA by improving reference libraries and amplifications, and enable a new breadth of population genetic studies.
引用
收藏
页码:283 / 294
页数:12
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