Sea anemones possess dynamic mitogenome structures.

Autor: Emblem Å; Department of Medical Biology, Faculty of Health Sciences, University of Tromsø, Norway., Okkenhaug S; Department of Medical Biology, Faculty of Health Sciences, University of Tromsø, Norway., Weiss ES; Department of Zoology, Oregon State University, USA., Denver DR; Department of Zoology, Oregon State University, USA., Karlsen BO; Department of Medical Biology, Faculty of Health Sciences, University of Tromsø, Norway; Marine Genomics group, Faculty of Biosciences and Aquaculture, University of Nordland, Norway., Moum T; Marine Genomics group, Faculty of Biosciences and Aquaculture, University of Nordland, Norway., Johansen SD; Department of Medical Biology, Faculty of Health Sciences, University of Tromsø, Norway; Marine Genomics group, Faculty of Biosciences and Aquaculture, University of Nordland, Norway. Electronic address: Steinar.Johansen@uit.no.
Jazyk: angličtina
Zdroj: Molecular phylogenetics and evolution [Mol Phylogenet Evol] 2014 Jun; Vol. 75, pp. 184-93. Date of Electronic Publication: 2014 Mar 06.
DOI: 10.1016/j.ympev.2014.02.016
Abstrakt: A notable feature of hexacoral mitogenomes is the presence of complex self-catalytic group I introns. We investigated mitogenome structural variations and evolutionary mechanisms in actiniarian sea anemones based on the complete mitogenome sequence of the cold-water sea anemone species Urticina eques, Bolocera tuediae, Hormathia digitata and Metridium senile, and two isolates of the sub-tropical Aiptasia pulchella. Whole genome sequencing at 50 times coverage of B. tuediae and H. digitata indicated low mtDNA copy number of per haploid nuclear genome and presence of rare haplotypes. A group I intron inserted in ND5 was found to host essential mitochondrial protein genes in all species, and an additional truncated copy of ND5 in B. tuediae. A second group I intron (inserted in COI) that contained a homing endonuclease gene (HEG) was present in all mtDNA examined. Different variants of HEGs were observed, and included expressed elements fused in-frame with upstream exons and free-standing HEGs embedded within the intron. A notable hallmark of HEGs was a high extent of overlap with ribozyme structural elements; the U. eques HEG overlapped with the entire intron. We reconstructed the evolutionary history of the COI intron from insertion at unoccupied cognate sites, through HEG degradation, to intron loss. We also identified a novel insertion element in U. eques that contained two expressed protein-coding genes. An evolutionary analysis of the sea anemone mtDNA genes revealed higher substitution rates in the HEG and the insertion sequence as compared to the other loci, indicating relaxed selective pressures in these elements. We conclude that sea anemone mitogenomes are surprisingly dynamic in structure despite the economical organization and low sequence mutation rate.
(Copyright © 2014 Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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