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The unique epigenetic features of Pack-MULEs and their impact on chromosomal base composition and expression spectrum

Acquisition and rearrangement of host genes by transposable elements (TEs) is an important mechanism to increase gene diversity as exemplified by the ∼3000 Pack-Mutator-like TEs in the rice genome which have acquired gene sequences (Pack-MULEs), yet remain enigmatic. To identify signatures of functi...

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Autores principales: Zhao, Dongyan, Hamilton, John P, Vaillancourt, Brieanne, Zhang, Wenli, Eizenga, Georgia C, Cui, Yuehua, Jiang, Jiming, Buell, C Robin, Jiang, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861414/
https://www.ncbi.nlm.nih.gov/pubmed/29365184
http://dx.doi.org/10.1093/nar/gky025
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author Zhao, Dongyan
Hamilton, John P
Vaillancourt, Brieanne
Zhang, Wenli
Eizenga, Georgia C
Cui, Yuehua
Jiang, Jiming
Buell, C Robin
Jiang, Ning
author_facet Zhao, Dongyan
Hamilton, John P
Vaillancourt, Brieanne
Zhang, Wenli
Eizenga, Georgia C
Cui, Yuehua
Jiang, Jiming
Buell, C Robin
Jiang, Ning
author_sort Zhao, Dongyan
collection PubMed
description Acquisition and rearrangement of host genes by transposable elements (TEs) is an important mechanism to increase gene diversity as exemplified by the ∼3000 Pack-Mutator-like TEs in the rice genome which have acquired gene sequences (Pack-MULEs), yet remain enigmatic. To identify signatures of functioning Pack-MULEs and Pack-MULE evolution, we generated transcriptome, translatome, and epigenome datasets and compared Pack-MULEs to genes and other TE families. Approximately 40% of Pack-MULEs were transcribed with 9% having translation evidence, clearly distinguishing them from other TEs. Pack-MULEs exhibited a unique expression profile associated with specificity in reproductive tissues that may be associated with seed traits. Expressed Pack-MULEs resemble regular protein-coding genes as exhibited by a low level of DNA methylation, association with active histone marks and DNase I hypersensitive sites, and an absence of repressive histone marks, suggesting that a substantial fraction of Pack-MULEs are potentially functional in vivo. Interestingly, the expression capacity of Pack-MULEs is independent of the local genomic environment, and the insertion and expression of Pack-MULEs may have altered the local chromosomal expression pattern as well as counteracted the impact of recombination on chromosomal base composition, which has profound consequences on the evolution of chromosome structure.
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spelling pubmed-58614142018-03-28 The unique epigenetic features of Pack-MULEs and their impact on chromosomal base composition and expression spectrum Zhao, Dongyan Hamilton, John P Vaillancourt, Brieanne Zhang, Wenli Eizenga, Georgia C Cui, Yuehua Jiang, Jiming Buell, C Robin Jiang, Ning Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Acquisition and rearrangement of host genes by transposable elements (TEs) is an important mechanism to increase gene diversity as exemplified by the ∼3000 Pack-Mutator-like TEs in the rice genome which have acquired gene sequences (Pack-MULEs), yet remain enigmatic. To identify signatures of functioning Pack-MULEs and Pack-MULE evolution, we generated transcriptome, translatome, and epigenome datasets and compared Pack-MULEs to genes and other TE families. Approximately 40% of Pack-MULEs were transcribed with 9% having translation evidence, clearly distinguishing them from other TEs. Pack-MULEs exhibited a unique expression profile associated with specificity in reproductive tissues that may be associated with seed traits. Expressed Pack-MULEs resemble regular protein-coding genes as exhibited by a low level of DNA methylation, association with active histone marks and DNase I hypersensitive sites, and an absence of repressive histone marks, suggesting that a substantial fraction of Pack-MULEs are potentially functional in vivo. Interestingly, the expression capacity of Pack-MULEs is independent of the local genomic environment, and the insertion and expression of Pack-MULEs may have altered the local chromosomal expression pattern as well as counteracted the impact of recombination on chromosomal base composition, which has profound consequences on the evolution of chromosome structure. Oxford University Press 2018-03-16 2018-01-22 /pmc/articles/PMC5861414/ /pubmed/29365184 http://dx.doi.org/10.1093/nar/gky025 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 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 Gene regulation, Chromatin and Epigenetics
Zhao, Dongyan
Hamilton, John P
Vaillancourt, Brieanne
Zhang, Wenli
Eizenga, Georgia C
Cui, Yuehua
Jiang, Jiming
Buell, C Robin
Jiang, Ning
The unique epigenetic features of Pack-MULEs and their impact on chromosomal base composition and expression spectrum
title The unique epigenetic features of Pack-MULEs and their impact on chromosomal base composition and expression spectrum
title_full The unique epigenetic features of Pack-MULEs and their impact on chromosomal base composition and expression spectrum
title_fullStr The unique epigenetic features of Pack-MULEs and their impact on chromosomal base composition and expression spectrum
title_full_unstemmed The unique epigenetic features of Pack-MULEs and their impact on chromosomal base composition and expression spectrum
title_short The unique epigenetic features of Pack-MULEs and their impact on chromosomal base composition and expression spectrum
title_sort unique epigenetic features of pack-mules and their impact on chromosomal base composition and expression spectrum
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861414/
https://www.ncbi.nlm.nih.gov/pubmed/29365184
http://dx.doi.org/10.1093/nar/gky025
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