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Domestication of High-Copy Transposons Underlays the Wheat Small RNA Response to an Obligate Pathogen
Plant genomes have evolved several evolutionary mechanisms to tolerate and make use of transposable elements (TEs). Of these, transposon domestication into cis-regulatory and microRNA (miRNA) sequences is proposed to contribute to abiotic/biotic stress adaptation in plants. The wheat genome is deriv...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038664/ https://www.ncbi.nlm.nih.gov/pubmed/31730193 http://dx.doi.org/10.1093/molbev/msz272 |
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author | Poretti, Manuel Praz, Coraline Rosalie Meile, Lukas Kälin, Carol Schaefer, Luisa Katharina Schläfli, Michael Widrig, Victoria Sanchez-Vallet, Andrea Wicker, Thomas Bourras, Salim |
author_facet | Poretti, Manuel Praz, Coraline Rosalie Meile, Lukas Kälin, Carol Schaefer, Luisa Katharina Schläfli, Michael Widrig, Victoria Sanchez-Vallet, Andrea Wicker, Thomas Bourras, Salim |
author_sort | Poretti, Manuel |
collection | PubMed |
description | Plant genomes have evolved several evolutionary mechanisms to tolerate and make use of transposable elements (TEs). Of these, transposon domestication into cis-regulatory and microRNA (miRNA) sequences is proposed to contribute to abiotic/biotic stress adaptation in plants. The wheat genome is derived at 85% from TEs, and contains thousands of miniature inverted-repeat transposable elements (MITEs), whose sequences are particularly prone for domestication into miRNA precursors. In this study, we investigate the contribution of TEs to the wheat small RNA immune response to the lineage-specific, obligate powdery mildew pathogen. We show that MITEs of the Mariner superfamily contribute the largest diversity of miRNAs to the wheat immune response. In particular, MITE precursors of miRNAs are wide-spread over the wheat genome, and highly conserved copies are found in the Lr34 and QPm.tut-4A mildew resistance loci. Our work suggests that transposon domestication is an important evolutionary force driving miRNA functional innovation in wheat immunity. |
format | Online Article Text |
id | pubmed-7038664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70386642020-03-02 Domestication of High-Copy Transposons Underlays the Wheat Small RNA Response to an Obligate Pathogen Poretti, Manuel Praz, Coraline Rosalie Meile, Lukas Kälin, Carol Schaefer, Luisa Katharina Schläfli, Michael Widrig, Victoria Sanchez-Vallet, Andrea Wicker, Thomas Bourras, Salim Mol Biol Evol Discoveries Plant genomes have evolved several evolutionary mechanisms to tolerate and make use of transposable elements (TEs). Of these, transposon domestication into cis-regulatory and microRNA (miRNA) sequences is proposed to contribute to abiotic/biotic stress adaptation in plants. The wheat genome is derived at 85% from TEs, and contains thousands of miniature inverted-repeat transposable elements (MITEs), whose sequences are particularly prone for domestication into miRNA precursors. In this study, we investigate the contribution of TEs to the wheat small RNA immune response to the lineage-specific, obligate powdery mildew pathogen. We show that MITEs of the Mariner superfamily contribute the largest diversity of miRNAs to the wheat immune response. In particular, MITE precursors of miRNAs are wide-spread over the wheat genome, and highly conserved copies are found in the Lr34 and QPm.tut-4A mildew resistance loci. Our work suggests that transposon domestication is an important evolutionary force driving miRNA functional innovation in wheat immunity. Oxford University Press 2020-03 2019-11-15 /pmc/articles/PMC7038664/ /pubmed/31730193 http://dx.doi.org/10.1093/molbev/msz272 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 | Discoveries Poretti, Manuel Praz, Coraline Rosalie Meile, Lukas Kälin, Carol Schaefer, Luisa Katharina Schläfli, Michael Widrig, Victoria Sanchez-Vallet, Andrea Wicker, Thomas Bourras, Salim Domestication of High-Copy Transposons Underlays the Wheat Small RNA Response to an Obligate Pathogen |
title | Domestication of High-Copy Transposons Underlays the Wheat Small RNA Response to an Obligate Pathogen |
title_full | Domestication of High-Copy Transposons Underlays the Wheat Small RNA Response to an Obligate Pathogen |
title_fullStr | Domestication of High-Copy Transposons Underlays the Wheat Small RNA Response to an Obligate Pathogen |
title_full_unstemmed | Domestication of High-Copy Transposons Underlays the Wheat Small RNA Response to an Obligate Pathogen |
title_short | Domestication of High-Copy Transposons Underlays the Wheat Small RNA Response to an Obligate Pathogen |
title_sort | domestication of high-copy transposons underlays the wheat small rna response to an obligate pathogen |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038664/ https://www.ncbi.nlm.nih.gov/pubmed/31730193 http://dx.doi.org/10.1093/molbev/msz272 |
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