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A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads

Identification of polymorphic transposable elements (TEs) is important because TE polymorphism creates genetic diversity and influences the function of genes in the host genome. However, de novo scanning of polymorphic TEs remains a challenge. Here, we report a novel computational method, called PTE...

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Autores principales: Kang, Houxiang, Zhu, Dan, Lin, Runmao, Opiyo, Stephen Obol, Jiang, Ning, Shiu, Shin-Han, Wang, Guo-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909310/
https://www.ncbi.nlm.nih.gov/pubmed/27098848
http://dx.doi.org/10.1093/dnares/dsw011
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author Kang, Houxiang
Zhu, Dan
Lin, Runmao
Opiyo, Stephen Obol
Jiang, Ning
Shiu, Shin-Han
Wang, Guo-Liang
author_facet Kang, Houxiang
Zhu, Dan
Lin, Runmao
Opiyo, Stephen Obol
Jiang, Ning
Shiu, Shin-Han
Wang, Guo-Liang
author_sort Kang, Houxiang
collection PubMed
description Identification of polymorphic transposable elements (TEs) is important because TE polymorphism creates genetic diversity and influences the function of genes in the host genome. However, de novo scanning of polymorphic TEs remains a challenge. Here, we report a novel computational method, called PTEMD (polymorphic TEs and their movement detection), for de novo discovery of genome-wide polymorphic TEs. PTEMD searches highly identical sequences using reads supported breakpoint evidences. Using PTEMD, we identified 14 polymorphic TE families (905 sequences) in rice blast fungus Magnaporthe oryzae, and 68 (10,618 sequences) in maize. We validated one polymorphic TE family experimentally, MoTE-1; all MoTE-1 family members are located in different genomic loci in the three tested isolates. We found that 57.1% (8 of 14) of the PTEMD-detected polymorphic TE families in M. oryzae are active. Furthermore, our data indicate that there are more polymorphic DNA transposons in maize than their counterparts of retrotransposons despite the fact that retrotransposons occupy largest fraction of genomic mass. We demonstrated that PTEMD is an effective tool for identifying polymorphic TEs in M. oryzae and maize genomes. PTEMD and the genome-wide polymorphic TEs in M. oryzae and maize are publically available at http://www.kanglab.cn/blast/PTEMD_V1.02.htm.
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spelling pubmed-49093102016-06-16 A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads Kang, Houxiang Zhu, Dan Lin, Runmao Opiyo, Stephen Obol Jiang, Ning Shiu, Shin-Han Wang, Guo-Liang DNA Res Full Papers Identification of polymorphic transposable elements (TEs) is important because TE polymorphism creates genetic diversity and influences the function of genes in the host genome. However, de novo scanning of polymorphic TEs remains a challenge. Here, we report a novel computational method, called PTEMD (polymorphic TEs and their movement detection), for de novo discovery of genome-wide polymorphic TEs. PTEMD searches highly identical sequences using reads supported breakpoint evidences. Using PTEMD, we identified 14 polymorphic TE families (905 sequences) in rice blast fungus Magnaporthe oryzae, and 68 (10,618 sequences) in maize. We validated one polymorphic TE family experimentally, MoTE-1; all MoTE-1 family members are located in different genomic loci in the three tested isolates. We found that 57.1% (8 of 14) of the PTEMD-detected polymorphic TE families in M. oryzae are active. Furthermore, our data indicate that there are more polymorphic DNA transposons in maize than their counterparts of retrotransposons despite the fact that retrotransposons occupy largest fraction of genomic mass. We demonstrated that PTEMD is an effective tool for identifying polymorphic TEs in M. oryzae and maize genomes. PTEMD and the genome-wide polymorphic TEs in M. oryzae and maize are publically available at http://www.kanglab.cn/blast/PTEMD_V1.02.htm. Oxford University Press 2016-06 2016-04-20 /pmc/articles/PMC4909310/ /pubmed/27098848 http://dx.doi.org/10.1093/dnares/dsw011 Text en © The Author 2016. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Full Papers
Kang, Houxiang
Zhu, Dan
Lin, Runmao
Opiyo, Stephen Obol
Jiang, Ning
Shiu, Shin-Han
Wang, Guo-Liang
A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads
title A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads
title_full A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads
title_fullStr A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads
title_full_unstemmed A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads
title_short A novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads
title_sort novel method for identifying polymorphic transposable elements via scanning of high-throughput short reads
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909310/
https://www.ncbi.nlm.nih.gov/pubmed/27098848
http://dx.doi.org/10.1093/dnares/dsw011
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