Cargando…

Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology

BACKGROUND: Transposables elements (TEs) contribute to both structural and functional dynamics of most eukaryotic genomes. Because of their propensity to densely populate plant and animal genomes, the precise estimation of the impact of transposition on genomic diversity has been considered as one o...

Descripción completa

Detalles Bibliográficos
Autores principales: Debladis, Emilie, Llauro, Christel, Carpentier, Marie-Christine, Mirouze, Marie, Panaud, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513335/
https://www.ncbi.nlm.nih.gov/pubmed/28715998
http://dx.doi.org/10.1186/s12864-017-3753-z
_version_ 1783250638622162944
author Debladis, Emilie
Llauro, Christel
Carpentier, Marie-Christine
Mirouze, Marie
Panaud, Olivier
author_facet Debladis, Emilie
Llauro, Christel
Carpentier, Marie-Christine
Mirouze, Marie
Panaud, Olivier
author_sort Debladis, Emilie
collection PubMed
description BACKGROUND: Transposables elements (TEs) contribute to both structural and functional dynamics of most eukaryotic genomes. Because of their propensity to densely populate plant and animal genomes, the precise estimation of the impact of transposition on genomic diversity has been considered as one of the main challenges of today’s genomics. The recent development of NGS (next generation sequencing) technologies has open new perspectives in population genomics by providing new methods for high throughput detection of Transposable Elements-associated Structural Variants (TEASV). However, these have relied on Illumina platform that generates short reads (up to 350 nucleotides). This limitation in size of sequence reads can cause high false discovery rate (FDR) and therefore limit the power of detection of TEASVs, especially in the case of large, complex genomes. The newest sequencing technologies, such as Oxford Nanopore Technologies (ONT) can generate kilobases-long reads thus representing a promising tool for TEASV detection in plant and animals. RESULTS: We present the results of a pilot experiment for TEASV detection on the model plant species Arabidopsis thaliana using ONT sequencing and show that it can be used efficiently to detect TE movements. We generated a ~0.8X genome coverage of a met1-derived epigenetic recombinant inbred line (epiRIL) using a MinIon device with R7 chemistry. We were able to detect nine new copies of the LTR-retrotransposon Evadé (EVD). We also evidenced the activity of the DNA transposon CACTA, CAC1. CONCLUSIONS: Even at a low sequence coverage (0.8X), ONT sequencing allowed us to reliably detect several TE insertions in Arabidopsis thaliana genome. The long read length allowed a precise and un-ambiguous mapping of the structural variations caused by the activity of TEs. This suggests that the trade-off between read length and genome coverage for TEASV detection may be in favor of the former. Should the technology be further improved both in terms of lower error rate and operation costs, it could be efficiently used in diversity studies at population level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3753-z) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5513335
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-55133352017-07-19 Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology Debladis, Emilie Llauro, Christel Carpentier, Marie-Christine Mirouze, Marie Panaud, Olivier BMC Genomics Methodology Article BACKGROUND: Transposables elements (TEs) contribute to both structural and functional dynamics of most eukaryotic genomes. Because of their propensity to densely populate plant and animal genomes, the precise estimation of the impact of transposition on genomic diversity has been considered as one of the main challenges of today’s genomics. The recent development of NGS (next generation sequencing) technologies has open new perspectives in population genomics by providing new methods for high throughput detection of Transposable Elements-associated Structural Variants (TEASV). However, these have relied on Illumina platform that generates short reads (up to 350 nucleotides). This limitation in size of sequence reads can cause high false discovery rate (FDR) and therefore limit the power of detection of TEASVs, especially in the case of large, complex genomes. The newest sequencing technologies, such as Oxford Nanopore Technologies (ONT) can generate kilobases-long reads thus representing a promising tool for TEASV detection in plant and animals. RESULTS: We present the results of a pilot experiment for TEASV detection on the model plant species Arabidopsis thaliana using ONT sequencing and show that it can be used efficiently to detect TE movements. We generated a ~0.8X genome coverage of a met1-derived epigenetic recombinant inbred line (epiRIL) using a MinIon device with R7 chemistry. We were able to detect nine new copies of the LTR-retrotransposon Evadé (EVD). We also evidenced the activity of the DNA transposon CACTA, CAC1. CONCLUSIONS: Even at a low sequence coverage (0.8X), ONT sequencing allowed us to reliably detect several TE insertions in Arabidopsis thaliana genome. The long read length allowed a precise and un-ambiguous mapping of the structural variations caused by the activity of TEs. This suggests that the trade-off between read length and genome coverage for TEASV detection may be in favor of the former. Should the technology be further improved both in terms of lower error rate and operation costs, it could be efficiently used in diversity studies at population level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3753-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-17 /pmc/articles/PMC5513335/ /pubmed/28715998 http://dx.doi.org/10.1186/s12864-017-3753-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Debladis, Emilie
Llauro, Christel
Carpentier, Marie-Christine
Mirouze, Marie
Panaud, Olivier
Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology
title Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology
title_full Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology
title_fullStr Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology
title_full_unstemmed Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology
title_short Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology
title_sort detection of active transposable elements in arabidopsis thaliana using oxford nanopore sequencing technology
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513335/
https://www.ncbi.nlm.nih.gov/pubmed/28715998
http://dx.doi.org/10.1186/s12864-017-3753-z
work_keys_str_mv AT debladisemilie detectionofactivetransposableelementsinarabidopsisthalianausingoxfordnanoporesequencingtechnology
AT llaurochristel detectionofactivetransposableelementsinarabidopsisthalianausingoxfordnanoporesequencingtechnology
AT carpentiermariechristine detectionofactivetransposableelementsinarabidopsisthalianausingoxfordnanoporesequencingtechnology
AT mirouzemarie detectionofactivetransposableelementsinarabidopsisthalianausingoxfordnanoporesequencingtechnology
AT panaudolivier detectionofactivetransposableelementsinarabidopsisthalianausingoxfordnanoporesequencingtechnology