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Preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome

Bromus tectorum L. is arguably the most successful invasive weed in the world. It has fundamentally altered arid ecosystems of the western United States, where it now found on an excess of 20 million hectares. Invasion success is related to avoidance of abiotic stress and human management. Early flo...

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Autores principales: Revolinski, Samuel R., Maughan, Peter J., Coleman, Craig E., Burke, Ian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10042881/
https://www.ncbi.nlm.nih.gov/pubmed/36973344
http://dx.doi.org/10.1038/s42003-023-04620-9
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author Revolinski, Samuel R.
Maughan, Peter J.
Coleman, Craig E.
Burke, Ian C.
author_facet Revolinski, Samuel R.
Maughan, Peter J.
Coleman, Craig E.
Burke, Ian C.
author_sort Revolinski, Samuel R.
collection PubMed
description Bromus tectorum L. is arguably the most successful invasive weed in the world. It has fundamentally altered arid ecosystems of the western United States, where it now found on an excess of 20 million hectares. Invasion success is related to avoidance of abiotic stress and human management. Early flowering is a heritable trait utilized by B. tectorum, enabling the species to temporally monopolize limited resources and outcompete the native plant community. Thus, understanding the genetic underpinning of flowering time is critical for the design of integrated management strategies. To study flowering time traits in B. tectorum, we assembled a chromosome scale reference genome for B. tectorum. To assess the utility of the assembled genome, 121 diverse B. tectorum accessions are phenotyped and subjected to a genome wide association study (GWAS). Candidate genes, representing homologs of genes that have been previously associated with plant height or flowering phenology traits in related species are located near QTLs we identified. This study uses a high-resolution GWAS to identify reproductive phenology genes in a weedy species and represents a considerable step forward in understanding the mechanisms underlying genetic plasticity in one of the most successful invasive weed species.
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spelling pubmed-100428812023-03-29 Preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome Revolinski, Samuel R. Maughan, Peter J. Coleman, Craig E. Burke, Ian C. Commun Biol Article Bromus tectorum L. is arguably the most successful invasive weed in the world. It has fundamentally altered arid ecosystems of the western United States, where it now found on an excess of 20 million hectares. Invasion success is related to avoidance of abiotic stress and human management. Early flowering is a heritable trait utilized by B. tectorum, enabling the species to temporally monopolize limited resources and outcompete the native plant community. Thus, understanding the genetic underpinning of flowering time is critical for the design of integrated management strategies. To study flowering time traits in B. tectorum, we assembled a chromosome scale reference genome for B. tectorum. To assess the utility of the assembled genome, 121 diverse B. tectorum accessions are phenotyped and subjected to a genome wide association study (GWAS). Candidate genes, representing homologs of genes that have been previously associated with plant height or flowering phenology traits in related species are located near QTLs we identified. This study uses a high-resolution GWAS to identify reproductive phenology genes in a weedy species and represents a considerable step forward in understanding the mechanisms underlying genetic plasticity in one of the most successful invasive weed species. Nature Publishing Group UK 2023-03-27 /pmc/articles/PMC10042881/ /pubmed/36973344 http://dx.doi.org/10.1038/s42003-023-04620-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Revolinski, Samuel R.
Maughan, Peter J.
Coleman, Craig E.
Burke, Ian C.
Preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome
title Preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome
title_full Preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome
title_fullStr Preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome
title_full_unstemmed Preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome
title_short Preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome
title_sort preadapted to adapt: underpinnings of adaptive plasticity revealed by the downy brome genome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10042881/
https://www.ncbi.nlm.nih.gov/pubmed/36973344
http://dx.doi.org/10.1038/s42003-023-04620-9
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