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Transposon Variants and Their Effects on Gene Expression in Arabidopsis

Transposable elements (TEs) make up the majority of many plant genomes. Their transcription and transposition is controlled through siRNAs and epigenetic marks including DNA methylation. To dissect the interplay of siRNA–mediated regulation and TE evolution, and to examine how TE differences affect...

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Autores principales: Wang, Xi, Weigel, Detlef, Smith, Lisa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3567156/
https://www.ncbi.nlm.nih.gov/pubmed/23408902
http://dx.doi.org/10.1371/journal.pgen.1003255
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author Wang, Xi
Weigel, Detlef
Smith, Lisa M.
author_facet Wang, Xi
Weigel, Detlef
Smith, Lisa M.
author_sort Wang, Xi
collection PubMed
description Transposable elements (TEs) make up the majority of many plant genomes. Their transcription and transposition is controlled through siRNAs and epigenetic marks including DNA methylation. To dissect the interplay of siRNA–mediated regulation and TE evolution, and to examine how TE differences affect nearby gene expression, we investigated genome-wide differences in TEs, siRNAs, and gene expression among three Arabidopsis thaliana accessions. Both TE sequence polymorphisms and presence of linked TEs are positively correlated with intraspecific variation in gene expression. The expression of genes within 2 kb of conserved TEs is more stable than that of genes next to variant TEs harboring sequence polymorphisms. Polymorphism levels of TEs and closely linked adjacent genes are positively correlated as well. We also investigated the distribution of 24-nt-long siRNAs, which mediate TE repression. TEs targeted by uniquely mapping siRNAs are on average farther from coding genes, apparently because they more strongly suppress expression of adjacent genes. Furthermore, siRNAs, and especially uniquely mapping siRNAs, are enriched in TE regions missing in other accessions. Thus, targeting by uniquely mapping siRNAs appears to promote sequence deletions in TEs. Overall, our work indicates that siRNA–targeting of TEs may influence removal of sequences from the genome and hence evolution of gene expression in plants.
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spelling pubmed-35671562013-02-13 Transposon Variants and Their Effects on Gene Expression in Arabidopsis Wang, Xi Weigel, Detlef Smith, Lisa M. PLoS Genet Research Article Transposable elements (TEs) make up the majority of many plant genomes. Their transcription and transposition is controlled through siRNAs and epigenetic marks including DNA methylation. To dissect the interplay of siRNA–mediated regulation and TE evolution, and to examine how TE differences affect nearby gene expression, we investigated genome-wide differences in TEs, siRNAs, and gene expression among three Arabidopsis thaliana accessions. Both TE sequence polymorphisms and presence of linked TEs are positively correlated with intraspecific variation in gene expression. The expression of genes within 2 kb of conserved TEs is more stable than that of genes next to variant TEs harboring sequence polymorphisms. Polymorphism levels of TEs and closely linked adjacent genes are positively correlated as well. We also investigated the distribution of 24-nt-long siRNAs, which mediate TE repression. TEs targeted by uniquely mapping siRNAs are on average farther from coding genes, apparently because they more strongly suppress expression of adjacent genes. Furthermore, siRNAs, and especially uniquely mapping siRNAs, are enriched in TE regions missing in other accessions. Thus, targeting by uniquely mapping siRNAs appears to promote sequence deletions in TEs. Overall, our work indicates that siRNA–targeting of TEs may influence removal of sequences from the genome and hence evolution of gene expression in plants. Public Library of Science 2013-02-07 /pmc/articles/PMC3567156/ /pubmed/23408902 http://dx.doi.org/10.1371/journal.pgen.1003255 Text en © 2013 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wang, Xi
Weigel, Detlef
Smith, Lisa M.
Transposon Variants and Their Effects on Gene Expression in Arabidopsis
title Transposon Variants and Their Effects on Gene Expression in Arabidopsis
title_full Transposon Variants and Their Effects on Gene Expression in Arabidopsis
title_fullStr Transposon Variants and Their Effects on Gene Expression in Arabidopsis
title_full_unstemmed Transposon Variants and Their Effects on Gene Expression in Arabidopsis
title_short Transposon Variants and Their Effects on Gene Expression in Arabidopsis
title_sort transposon variants and their effects on gene expression in arabidopsis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3567156/
https://www.ncbi.nlm.nih.gov/pubmed/23408902
http://dx.doi.org/10.1371/journal.pgen.1003255
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