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The genetic architecture of flowering time changes in pea from wild to crop

Change in phenology has been an important component in crop evolution, and selection for earlier flowering through a reduction in environmental sensitivity has helped broaden adaptation in many species. Natural variation for flowering in domesticated pea (Pisum sativum L.) has been noted and studied...

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Autores principales: Williams, Owen, Vander Schoor, Jacqueline K, Butler, Jakob B, Ridge, Stephen, Sussmilch, Frances C, Hecht, Valerie F G, Weller, James L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238443/
https://www.ncbi.nlm.nih.gov/pubmed/35383838
http://dx.doi.org/10.1093/jxb/erac132
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author Williams, Owen
Vander Schoor, Jacqueline K
Butler, Jakob B
Ridge, Stephen
Sussmilch, Frances C
Hecht, Valerie F G
Weller, James L
author_facet Williams, Owen
Vander Schoor, Jacqueline K
Butler, Jakob B
Ridge, Stephen
Sussmilch, Frances C
Hecht, Valerie F G
Weller, James L
author_sort Williams, Owen
collection PubMed
description Change in phenology has been an important component in crop evolution, and selection for earlier flowering through a reduction in environmental sensitivity has helped broaden adaptation in many species. Natural variation for flowering in domesticated pea (Pisum sativum L.) has been noted and studied for decades, but there has been no clear account of change relative to its wild progenitor. Here we examined the genetic control of differences in flowering time between wild P. sativum ssp. humile and a typical late-flowering photoperiodic P. s. sativum accession in a recombinant inbred population under long and short photoperiods. Our results confirm the importance of the major photoperiod sensitivity locus Hr/PsELF3a and identify two other loci on chromosomes 1 (DTF1) and 3 (DTF3) that contribute to earlier flowering in the domesticated line under both photoperiods. The domesticated allele at a fourth locus on chromosome 6 (DTF6) delays flowering under long days only. Map positions, inheritance patterns, and expression analyses in near-isogenic comparisons imply that DTF1, DTF3, and DTF6 represent gain-of-function alleles of the florigen/antiflorigen genes FTa3, FTa1, and TFL1c/LF, respectively. This echoes similar variation in chickpea and lentil, and suggests a conserved route to reduced photoperiod sensitivity and early phenology in temperate pulses.
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spelling pubmed-92384432022-06-29 The genetic architecture of flowering time changes in pea from wild to crop Williams, Owen Vander Schoor, Jacqueline K Butler, Jakob B Ridge, Stephen Sussmilch, Frances C Hecht, Valerie F G Weller, James L J Exp Bot Research Papers Change in phenology has been an important component in crop evolution, and selection for earlier flowering through a reduction in environmental sensitivity has helped broaden adaptation in many species. Natural variation for flowering in domesticated pea (Pisum sativum L.) has been noted and studied for decades, but there has been no clear account of change relative to its wild progenitor. Here we examined the genetic control of differences in flowering time between wild P. sativum ssp. humile and a typical late-flowering photoperiodic P. s. sativum accession in a recombinant inbred population under long and short photoperiods. Our results confirm the importance of the major photoperiod sensitivity locus Hr/PsELF3a and identify two other loci on chromosomes 1 (DTF1) and 3 (DTF3) that contribute to earlier flowering in the domesticated line under both photoperiods. The domesticated allele at a fourth locus on chromosome 6 (DTF6) delays flowering under long days only. Map positions, inheritance patterns, and expression analyses in near-isogenic comparisons imply that DTF1, DTF3, and DTF6 represent gain-of-function alleles of the florigen/antiflorigen genes FTa3, FTa1, and TFL1c/LF, respectively. This echoes similar variation in chickpea and lentil, and suggests a conserved route to reduced photoperiod sensitivity and early phenology in temperate pulses. Oxford University Press 2022-04-06 /pmc/articles/PMC9238443/ /pubmed/35383838 http://dx.doi.org/10.1093/jxb/erac132 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Experimental Biology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Williams, Owen
Vander Schoor, Jacqueline K
Butler, Jakob B
Ridge, Stephen
Sussmilch, Frances C
Hecht, Valerie F G
Weller, James L
The genetic architecture of flowering time changes in pea from wild to crop
title The genetic architecture of flowering time changes in pea from wild to crop
title_full The genetic architecture of flowering time changes in pea from wild to crop
title_fullStr The genetic architecture of flowering time changes in pea from wild to crop
title_full_unstemmed The genetic architecture of flowering time changes in pea from wild to crop
title_short The genetic architecture of flowering time changes in pea from wild to crop
title_sort genetic architecture of flowering time changes in pea from wild to crop
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238443/
https://www.ncbi.nlm.nih.gov/pubmed/35383838
http://dx.doi.org/10.1093/jxb/erac132
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