| Literature DB >> 28222945 |
Quentin Blandenier1, Enrique Lara2, Edward A D Mitchell3, Daniel M C Alcantara4, Ferry J Siemensma5, Milcho Todorov6, Daniel J G Lahr7.
Abstract
Molecular phylogeny is an indispensable tool for assessing evolutionary relationships among protists. The most commonly used marker is the small subunit ribosomal RNA gene, a conserved gene present in many copies in the nuclear genomes. However, this marker is not variable enough at a fine-level taxonomic scale, and intra-genomic polymorphism has already been reported. Finding a marker that could be useful at both deep and fine taxonomic resolution levels seemed like a utopic dream. We designed Amoebozoa-specific primers to amplify a region including partial sequences of two subunits of the mitochondrial nicotinamide adenine dinucleotide dehydrogenase gene (NAD9/NAD7). We applied them to arcellinids belonging to distantly related genera (Arcella, Difflugia, Netzelia and Hyalosphenia) and to Arcellinid-rich environmental samples to obtain additional Amoebozoa sequences. Tree topology was congruent with previous phylogenies, all nodes being highly supported, suggesting that this marker is well-suited for deep phylogenies in Arcellinida and perhaps Amoebozoa. Furthermore, it enabled discrimination of close-related taxa. This short genetic marker (ca. 250bp) can therefore be used at different taxonomic levels, due to a fast-varying intergenic region presenting either a small intergenic sequence or an overlap, depending on the species.Entities:
Keywords: Arcella; Environmental DNA survey; Intergenic region; Mitochondrion; Molecular barcoding
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Year: 2016 PMID: 28222945 DOI: 10.1016/j.ejop.2016.12.002
Source DB: PubMed Journal: Eur J Protistol ISSN: 0932-4739 Impact factor: 3.020