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Evolution of Group I Introns in Porifera: New Evidence for Intron Mobility and Implications for DNA Barcoding

  • Astrid Schuster
  • , Jose V Lopez
  • , Leontine E. Becking
  • , Michelle Kelly
  • , Shirley A. Pomponi
  • , Gert Wörheide
  • , Dirk Erpenbeck
  • , Paco Cárdenas

Research output: Contribution to journal › Article › peer-review

Abstract

Background
Mitochondrial introns intermit coding regions of genes and feature characteristic secondary structures and splicing mechanisms. In metazoans, mitochondrial introns have only been detected in sponges, cnidarians, placozoans and one annelid species. Within demosponges, group I and group II introns are present in six families. Based on different insertion sites within the cox 1 gene and secondary structures, four types of group I and two types of group II introns are known, which can harbor up to three encoding homing endonuclease genes (HEG) of the LAGLIDADG family (group I) and/or reverse transcriptase (group II). However, only little is known about sponge intron mobility, transmission, and origin due to the lack of a comprehensive dataset. We analyzed the largest dataset on sponge mitochondrial group I introns to date: 95 specimens, from 11 different sponge genera which provided novel insights into the evolution of group I introns.

Results
For the first time group I introns were detected in four genera of the sponge family Scleritodermidae ( Scleritoderma, Microscleroderma, Aciculites, Setidium ). We demonstrated that group I introns in sponges aggregate in the most conserved regions of cox 1. We showed that co-occurrence of two introns in cox 1 is unique among metazoans, but not uncommon in sponges. However, this combination always associates an active intron with a degenerating one. Earlier hypotheses of HGT were confirmed and for the first time VGT and secondary losses of introns conclusively demonstrated.

Conclusion
This study validates the subclass Spirophorina (Tetractinellida) as an intron hotspot in sponges. Our analyses confirm that most sponge group I introns probably originated from fungi. DNA barcoding is discussed and the application of alternative primers suggested.

Original languageAmerican English
Article number82
Number of pages21
JournalBMC Evolutionary Biology
Volume17
Issue number1
DOIs
StatePublished - Mar 20 2017

Bibliographical note

Publisher Copyright:
© 2017 The Author(s).

Funding

This work was funded by the German Science Foundation (DFG) (grant number DFG ER 611/3-1, DFG Wo896/15-1); LMUMentoring Program; HELGE AX:Son JOHNSON STIFTELSE (Sweden), Inez Johanssons HT2012 (Uppsala University, Sweden) and Netherlands Organisation for Scientific Research (NWO) Veni#863.14.020.

FundersFunder number
Deutsche ForschungsgemeinschaftDFG Wo896/15-1, DFG ER 611/3-1, HT2012
Nederlandse Organisatie voor Wetenschappelijk Onderzoek863.14.020
Uppsala Universitet

    ASJC Scopus Subject Areas

    • Ecology, Evolution, Behavior and Systematics

    Keywords

    • DNA barcoding
    • Group I intron
    • HGT
    • Homing endonuclease gene (HEG)
    • LAGLIDADG
    • Porifera
    • Tetractinellida
    • VGT
    • cox1
    • homing endonuclease gene (HEG)
    • group I intron
    • Endonucleases/genetics
    • Introns
    • Open Reading Frames
    • Phylogeny
    • DNA Barcoding, Taxonomic
    • Biological Evolution
    • RNA Splicing
    • Animals
    • Base Sequence
    • Porifera/classification
    • Mitochondria/genetics

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