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

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...

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Autores principales: Grabundzija, Ivana, Messing, Simon A., Thomas, Jainy, Cosby, Rachel L., Bilic, Ilija, Miskey, Csaba, Gogol-Döring, Andreas, Kapitonov, Vladimir, Diem, Tanja, Dalda, Anna, Jurka, Jerzy, Pritham, Ellen J., Dyda, Fred, Izsvák, Zsuzsanna, Ivics, Zoltán
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778049/
https://www.ncbi.nlm.nih.gov/pubmed/26931494
http://dx.doi.org/10.1038/ncomms10716
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author Grabundzija, Ivana
Messing, Simon A.
Thomas, Jainy
Cosby, Rachel L.
Bilic, Ilija
Miskey, Csaba
Gogol-Döring, Andreas
Kapitonov, Vladimir
Diem, Tanja
Dalda, Anna
Jurka, Jerzy
Pritham, Ellen J.
Dyda, Fred
Izsvák, Zsuzsanna
Ivics, Zoltán
author_facet Grabundzija, Ivana
Messing, Simon A.
Thomas, Jainy
Cosby, Rachel L.
Bilic, Ilija
Miskey, Csaba
Gogol-Döring, Andreas
Kapitonov, Vladimir
Diem, Tanja
Dalda, Anna
Jurka, Jerzy
Pritham, Ellen J.
Dyda, Fred
Izsvák, Zsuzsanna
Ivics, Zoltán
author_sort Grabundzija, Ivana
collection PubMed
description 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.
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spelling pubmed-47780492016-03-04 A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes Grabundzija, Ivana Messing, Simon A. Thomas, Jainy Cosby, Rachel L. Bilic, Ilija Miskey, Csaba Gogol-Döring, Andreas Kapitonov, Vladimir Diem, Tanja Dalda, Anna Jurka, Jerzy Pritham, Ellen J. Dyda, Fred Izsvák, Zsuzsanna Ivics, Zoltán Nat Commun Article 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. Nature Publishing Group 2016-03-02 /pmc/articles/PMC4778049/ /pubmed/26931494 http://dx.doi.org/10.1038/ncomms10716 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Grabundzija, Ivana
Messing, Simon A.
Thomas, Jainy
Cosby, Rachel L.
Bilic, Ilija
Miskey, Csaba
Gogol-Döring, Andreas
Kapitonov, Vladimir
Diem, Tanja
Dalda, Anna
Jurka, Jerzy
Pritham, Ellen J.
Dyda, Fred
Izsvák, Zsuzsanna
Ivics, Zoltán
A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes
title A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes
title_full A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes
title_fullStr A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes
title_full_unstemmed A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes
title_short A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes
title_sort helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778049/
https://www.ncbi.nlm.nih.gov/pubmed/26931494
http://dx.doi.org/10.1038/ncomms10716
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