Cargando…

Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions

Miniature inverted repeat transposable elements (MITEs) are prevalent in eukaryotic genomes. They are known to critically influence the process of genome evolution and play a role in gene regulation. As the first study concentrated in the transposition activities of MITEs among different ecotype acc...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Cheng, Spinelli, Matthew, Ye, Congting, Li, Qingshun Q., Liang, Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454002/
https://www.ncbi.nlm.nih.gov/pubmed/28572566
http://dx.doi.org/10.1038/s41598-017-02855-1
_version_ 1783240757309603840
author Guo, Cheng
Spinelli, Matthew
Ye, Congting
Li, Qingshun Q.
Liang, Chun
author_facet Guo, Cheng
Spinelli, Matthew
Ye, Congting
Li, Qingshun Q.
Liang, Chun
author_sort Guo, Cheng
collection PubMed
description Miniature inverted repeat transposable elements (MITEs) are prevalent in eukaryotic genomes. They are known to critically influence the process of genome evolution and play a role in gene regulation. As the first study concentrated in the transposition activities of MITEs among different ecotype accessions within a species, we conducted a genome-wide comparative analysis by characterizing and comparing MITEs in 19 Arabidopsis thaliana accessions. A total of 343485 MITE putative sequences, including canonical, diverse and partial ones, were delineated from all 19 accessions. Within the entire population of MITEs sequences, 80.7% of them were previously unclassified MITEs, demonstrating a different genomic distribution and functionality compared to the classified MITEs. The interactions between MITEs and homologous genes across 19 accessions provided a fine source for analyzing MITE transposition activities and their impacts on genome evolution. Moreover, a significant proportion of MITEs were found located in the last exon of genes besides the ordinary intron locality, thus potentially modifying the end of genes. Finally, analysis of the impact of MITEs on gene expression suggests that migrations of MITEs have no detectable effect on the expression level for host genes across accessions.
format Online
Article
Text
id pubmed-5454002
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-54540022017-06-06 Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions Guo, Cheng Spinelli, Matthew Ye, Congting Li, Qingshun Q. Liang, Chun Sci Rep Article Miniature inverted repeat transposable elements (MITEs) are prevalent in eukaryotic genomes. They are known to critically influence the process of genome evolution and play a role in gene regulation. As the first study concentrated in the transposition activities of MITEs among different ecotype accessions within a species, we conducted a genome-wide comparative analysis by characterizing and comparing MITEs in 19 Arabidopsis thaliana accessions. A total of 343485 MITE putative sequences, including canonical, diverse and partial ones, were delineated from all 19 accessions. Within the entire population of MITEs sequences, 80.7% of them were previously unclassified MITEs, demonstrating a different genomic distribution and functionality compared to the classified MITEs. The interactions between MITEs and homologous genes across 19 accessions provided a fine source for analyzing MITE transposition activities and their impacts on genome evolution. Moreover, a significant proportion of MITEs were found located in the last exon of genes besides the ordinary intron locality, thus potentially modifying the end of genes. Finally, analysis of the impact of MITEs on gene expression suggests that migrations of MITEs have no detectable effect on the expression level for host genes across accessions. Nature Publishing Group UK 2017-06-01 /pmc/articles/PMC5454002/ /pubmed/28572566 http://dx.doi.org/10.1038/s41598-017-02855-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Guo, Cheng
Spinelli, Matthew
Ye, Congting
Li, Qingshun Q.
Liang, Chun
Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions
title Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions
title_full Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions
title_fullStr Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions
title_full_unstemmed Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions
title_short Genome-Wide Comparative Analysis of Miniature Inverted Repeat Transposable Elements in 19 Arabidopsis thaliana Ecotype Accessions
title_sort genome-wide comparative analysis of miniature inverted repeat transposable elements in 19 arabidopsis thaliana ecotype accessions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454002/
https://www.ncbi.nlm.nih.gov/pubmed/28572566
http://dx.doi.org/10.1038/s41598-017-02855-1
work_keys_str_mv AT guocheng genomewidecomparativeanalysisofminiatureinvertedrepeattransposableelementsin19arabidopsisthalianaecotypeaccessions
AT spinellimatthew genomewidecomparativeanalysisofminiatureinvertedrepeattransposableelementsin19arabidopsisthalianaecotypeaccessions
AT yecongting genomewidecomparativeanalysisofminiatureinvertedrepeattransposableelementsin19arabidopsisthalianaecotypeaccessions
AT liqingshunq genomewidecomparativeanalysisofminiatureinvertedrepeattransposableelementsin19arabidopsisthalianaecotypeaccessions
AT liangchun genomewidecomparativeanalysisofminiatureinvertedrepeattransposableelementsin19arabidopsisthalianaecotypeaccessions