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A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes

Author

Listed:
  • Ivana Grabundzija

    (Max Delbrück Center for Molecular Medicine
    Laboratory of Molecular Biology)

  • Simon A. Messing

    (Laboratory of Molecular Biology)

  • Jainy Thomas

    (University of Utah)

  • Rachel L. Cosby

    (University of Utah)

  • Ilija Bilic

    (Max Delbrück Center for Molecular Medicine)

  • Csaba Miskey

    (Paul Ehrlich Institute)

  • Andreas Gogol-Döring

    (German Center of Integrative Biodiversity Research (iDiv)
    Institute of Computer Science, Martin Luther University Halle–Wittenberg)

  • Vladimir Kapitonov

    (Genetic Information Research Institute)

  • Tanja Diem

    (Paul Ehrlich Institute)

  • Anna Dalda

    (Max Delbrück Center for Molecular Medicine)

  • Jerzy Jurka

    (Genetic Information Research Institute)

  • Ellen J. Pritham

    (University of Utah)

  • Fred Dyda

    (Laboratory of Molecular Biology)

  • Zsuzsanna Izsvák

    (Max Delbrück Center for Molecular Medicine)

  • Zoltán Ivics

    (Paul Ehrlich Institute)

Abstract

Helitron transposons capture and mobilize gene fragments in eukaryotes, but experimental evidence for their transposition is lacking in the absence of an isolated active element. Here we reconstruct Helraiser, an ancient element from the bat genome, and use this transposon as an experimental tool to unravel the mechanism of Helitron transposition. A hairpin close to the 3′-end of the transposon functions as a transposition terminator. However, the 3′-end can be bypassed by the transposase, resulting in transduction of flanking sequences to new genomic locations. Helraiser transposition generates covalently closed circular intermediates, suggestive of a replicative transposition mechanism, which provides a powerful means to disseminate captured transcriptional regulatory signals across the genome. Indeed, we document the generation of novel transcripts by Helitron promoter capture both experimentally and by transcriptome analysis in bats. Our results provide mechanistic insight into Helitron transposition, and its impact on diversification of gene function by genome shuffling.

Suggested Citation

  • Ivana Grabundzija & Simon A. Messing & Jainy Thomas & Rachel L. Cosby & Ilija Bilic & Csaba Miskey & Andreas Gogol-Döring & Vladimir Kapitonov & Tanja Diem & Anna Dalda & Jerzy Jurka & Ellen J. Pritha, 2016. "A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes," Nature Communications, Nature, vol. 7(1), pages 1-12, April.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10716
    DOI: 10.1038/ncomms10716
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    Cited by:

    1. Marine Duhamel & Michael E. Hood & Ricardo C. Rodríguez de la Vega & Tatiana Giraud, 2023. "Dynamics of transposable element accumulation in the non-recombining regions of mating-type chromosomes in anther-smut fungi," Nature Communications, Nature, vol. 14(1), pages 1-18, December.

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