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  4. NAD9/NAD7 (mitochondrial nicotinamide adenine dinucleotide dehydrogenase gene): A new “Holy Grail” phylogenetic and DNA-barcoding marker for Arcellinida (Amoebozoa)?

NAD9/NAD7 (mitochondrial nicotinamide adenine dinucleotide dehydrogenase gene): A new “Holy Grail” phylogenetic and DNA-barcoding marker for Arcellinida (Amoebozoa)?

Author(s)
Blandenier, Quentin  
Laboratoire de biodiversité du sol  
Lara, Enrique  
Laboratoire de biodiversité du sol  
Mitchell, Edward  
Laboratoire de biodiversité du sol  
Alcantara, Daniel M.C
Siemensma, Ferry J
Todorov, Milcho
Lahr, Daniel J.G
Date issued
2017
In
European Journal of Protistology, Elsevier
Vol
58
From page
175
To page
186
Subjects
<i>Arcella</i> Environmental DNA survey Intergenic region Mitochondrion Molecular barcoding
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 (<i>Arcella</i>, <i>Difflugia</i>, <i>Netzelia</i> and <i>Hyalosphenia</i>) 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. 250 bp) 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.
Publication type
journal article
Identifiers
https://libra.unine.ch/handle/20.500.14713/65182
DOI
10.1016/j.ejop.2016.12.002
-
https://libra.unine.ch/handle/123456789/4807
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