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Trait analysis reveals DOG1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing

Seedling emergence timing is crucial in competitive plant communities and so contributes to species fitness. To understand the mechanistic basis of variation in seedling emergence timing, we exploited the contrasting behaviour of two Arabidopsis thaliana ecotypes: Cape Verde Islands (Cvi) and Burren...

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Autores principales: Footitt, Steven, Walley, Peter G., Lynn, James R., Hambidge, Angela J., Penfield, Steven, Finch‐Savage, William E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027856/
https://www.ncbi.nlm.nih.gov/pubmed/31359436
http://dx.doi.org/10.1111/nph.16081
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author Footitt, Steven
Walley, Peter G.
Lynn, James R.
Hambidge, Angela J.
Penfield, Steven
Finch‐Savage, William E.
author_facet Footitt, Steven
Walley, Peter G.
Lynn, James R.
Hambidge, Angela J.
Penfield, Steven
Finch‐Savage, William E.
author_sort Footitt, Steven
collection PubMed
description Seedling emergence timing is crucial in competitive plant communities and so contributes to species fitness. To understand the mechanistic basis of variation in seedling emergence timing, we exploited the contrasting behaviour of two Arabidopsis thaliana ecotypes: Cape Verde Islands (Cvi) and Burren (Bur‐0). We used RNA‐Seq analysis of RNA from exhumed seeds and quantitative trait loci (QTL) analyses on a mapping population from crossing the Cvi and Bur‐0 ecotypes. We determined genome‐wide expression patterns over an annual dormancy cycle in both ecotypes, identifying nine major clusters based on the seasonal timing of gene expression, and variation in behaviour between them. QTL were identified for depth of seed dormancy and seedling emergence timing (SET). Both analyses showed a key role for DOG1 in determining depth of dormancy, but did not support a direct role for DOG1 in generating altered seasonal patterns of seedling emergence. The principle QTL determining SET (SET1: dormancy cycling) is physically close on chromosome 5, but is distinct from DOG1. We show that SET1 and two other SET QTLs each contain a candidate gene (AHG1, ANAC060, PDF1 respectively) closely associated with DOG1 and abscisic acid signalling and suggest a model for the control of SET in the field.
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spelling pubmed-70278562020-02-24 Trait analysis reveals DOG1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing Footitt, Steven Walley, Peter G. Lynn, James R. Hambidge, Angela J. Penfield, Steven Finch‐Savage, William E. New Phytol Research Seedling emergence timing is crucial in competitive plant communities and so contributes to species fitness. To understand the mechanistic basis of variation in seedling emergence timing, we exploited the contrasting behaviour of two Arabidopsis thaliana ecotypes: Cape Verde Islands (Cvi) and Burren (Bur‐0). We used RNA‐Seq analysis of RNA from exhumed seeds and quantitative trait loci (QTL) analyses on a mapping population from crossing the Cvi and Bur‐0 ecotypes. We determined genome‐wide expression patterns over an annual dormancy cycle in both ecotypes, identifying nine major clusters based on the seasonal timing of gene expression, and variation in behaviour between them. QTL were identified for depth of seed dormancy and seedling emergence timing (SET). Both analyses showed a key role for DOG1 in determining depth of dormancy, but did not support a direct role for DOG1 in generating altered seasonal patterns of seedling emergence. The principle QTL determining SET (SET1: dormancy cycling) is physically close on chromosome 5, but is distinct from DOG1. We show that SET1 and two other SET QTLs each contain a candidate gene (AHG1, ANAC060, PDF1 respectively) closely associated with DOG1 and abscisic acid signalling and suggest a model for the control of SET in the field. John Wiley and Sons Inc. 2019-09-18 2020-03 /pmc/articles/PMC7027856/ /pubmed/31359436 http://dx.doi.org/10.1111/nph.16081 Text en © 2019 The Authors. New Phytologist © 2019 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Footitt, Steven
Walley, Peter G.
Lynn, James R.
Hambidge, Angela J.
Penfield, Steven
Finch‐Savage, William E.
Trait analysis reveals DOG1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing
title Trait analysis reveals DOG1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing
title_full Trait analysis reveals DOG1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing
title_fullStr Trait analysis reveals DOG1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing
title_full_unstemmed Trait analysis reveals DOG1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing
title_short Trait analysis reveals DOG1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing
title_sort trait analysis reveals dog1 determines initial depth of seed dormancy, but not changes during dormancy cycling that result in seedling emergence timing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027856/
https://www.ncbi.nlm.nih.gov/pubmed/31359436
http://dx.doi.org/10.1111/nph.16081
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