Cargando…

Characterization and quantitative trait locus mapping of late-flowering from a Thai soybean cultivar introduced into a photoperiod-insensitive genetic background

The timing of both flowering and maturation determine crop adaptability and productivity. Soybean (Glycine max) is cultivated across a wide range of latitudes. The molecular-genetic mechanisms for flowering in soybean have been determined for photoperiodic responses to long days (LDs), but remain on...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Fei, Xu, Meilan, Park, Cheolwoo, Dwiyanti, Maria Stefanie, Nagano, Atsushi J., Zhu, Jianghui, Watanabe, Satoshi, Kong, Fanjiang, Liu, Baohui, Yamada, Tetsuya, Abe, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894811/
https://www.ncbi.nlm.nih.gov/pubmed/31805143
http://dx.doi.org/10.1371/journal.pone.0226116
_version_ 1783476461166919680
author Sun, Fei
Xu, Meilan
Park, Cheolwoo
Dwiyanti, Maria Stefanie
Nagano, Atsushi J.
Zhu, Jianghui
Watanabe, Satoshi
Kong, Fanjiang
Liu, Baohui
Yamada, Tetsuya
Abe, Jun
author_facet Sun, Fei
Xu, Meilan
Park, Cheolwoo
Dwiyanti, Maria Stefanie
Nagano, Atsushi J.
Zhu, Jianghui
Watanabe, Satoshi
Kong, Fanjiang
Liu, Baohui
Yamada, Tetsuya
Abe, Jun
author_sort Sun, Fei
collection PubMed
description The timing of both flowering and maturation determine crop adaptability and productivity. Soybean (Glycine max) is cultivated across a wide range of latitudes. The molecular-genetic mechanisms for flowering in soybean have been determined for photoperiodic responses to long days (LDs), but remain only partially determined for the delay of flowering under short-day conditions, an adaptive trait of cultivars grown in lower latitudes. Here, we characterized the late-flowering (LF) habit introduced from the Thai cultivar K3 into a photoperiod-insensitive genetic background under different photo-thermal conditions, and we analyzed the genetic basis using quantitative trait locus (QTL) mapping. The LF habit resulted from a basic difference in the floral induction activity and from the suppression of flowering, which was caused by red light-enriched LD lengths and higher temperatures, during which FLOWERING LOCUS T (FT) orthologs, FT2a and FT5a, were strongly down-regulated. QTL mapping using gene-specific markers for flowering genes E2, FT2a and FT5a and 829 single nucleotide polymorphisms obtained from restriction-site associated DNA sequencing detected three QTLs controlling the LF habit. Of these, a QTL harboring FT2a exhibited large and stable effects under all the conditions tested. A resequencing analysis detected a nonsynonymous substitution in exon 4 of FT2a from K3, which converted the glycine conserved in FT-like proteins to the aspartic acid conserved in TERMINAL FLOWER 1-like proteins (floral repressors), suggesting a functional depression in the FT2a protein from K3. The effects of the remaining two QTLs, likely corresponding to E2 and FT5a, were environment dependent. Thus, the LF habit from K3 may be caused by the functional depression of FT2a and the down-regulation of two FT genes by red light-enriched LD conditions and high temperatures.
format Online
Article
Text
id pubmed-6894811
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-68948112019-12-14 Characterization and quantitative trait locus mapping of late-flowering from a Thai soybean cultivar introduced into a photoperiod-insensitive genetic background Sun, Fei Xu, Meilan Park, Cheolwoo Dwiyanti, Maria Stefanie Nagano, Atsushi J. Zhu, Jianghui Watanabe, Satoshi Kong, Fanjiang Liu, Baohui Yamada, Tetsuya Abe, Jun PLoS One Research Article The timing of both flowering and maturation determine crop adaptability and productivity. Soybean (Glycine max) is cultivated across a wide range of latitudes. The molecular-genetic mechanisms for flowering in soybean have been determined for photoperiodic responses to long days (LDs), but remain only partially determined for the delay of flowering under short-day conditions, an adaptive trait of cultivars grown in lower latitudes. Here, we characterized the late-flowering (LF) habit introduced from the Thai cultivar K3 into a photoperiod-insensitive genetic background under different photo-thermal conditions, and we analyzed the genetic basis using quantitative trait locus (QTL) mapping. The LF habit resulted from a basic difference in the floral induction activity and from the suppression of flowering, which was caused by red light-enriched LD lengths and higher temperatures, during which FLOWERING LOCUS T (FT) orthologs, FT2a and FT5a, were strongly down-regulated. QTL mapping using gene-specific markers for flowering genes E2, FT2a and FT5a and 829 single nucleotide polymorphisms obtained from restriction-site associated DNA sequencing detected three QTLs controlling the LF habit. Of these, a QTL harboring FT2a exhibited large and stable effects under all the conditions tested. A resequencing analysis detected a nonsynonymous substitution in exon 4 of FT2a from K3, which converted the glycine conserved in FT-like proteins to the aspartic acid conserved in TERMINAL FLOWER 1-like proteins (floral repressors), suggesting a functional depression in the FT2a protein from K3. The effects of the remaining two QTLs, likely corresponding to E2 and FT5a, were environment dependent. Thus, the LF habit from K3 may be caused by the functional depression of FT2a and the down-regulation of two FT genes by red light-enriched LD conditions and high temperatures. Public Library of Science 2019-12-05 /pmc/articles/PMC6894811/ /pubmed/31805143 http://dx.doi.org/10.1371/journal.pone.0226116 Text en © 2019 Sun 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sun, Fei
Xu, Meilan
Park, Cheolwoo
Dwiyanti, Maria Stefanie
Nagano, Atsushi J.
Zhu, Jianghui
Watanabe, Satoshi
Kong, Fanjiang
Liu, Baohui
Yamada, Tetsuya
Abe, Jun
Characterization and quantitative trait locus mapping of late-flowering from a Thai soybean cultivar introduced into a photoperiod-insensitive genetic background
title Characterization and quantitative trait locus mapping of late-flowering from a Thai soybean cultivar introduced into a photoperiod-insensitive genetic background
title_full Characterization and quantitative trait locus mapping of late-flowering from a Thai soybean cultivar introduced into a photoperiod-insensitive genetic background
title_fullStr Characterization and quantitative trait locus mapping of late-flowering from a Thai soybean cultivar introduced into a photoperiod-insensitive genetic background
title_full_unstemmed Characterization and quantitative trait locus mapping of late-flowering from a Thai soybean cultivar introduced into a photoperiod-insensitive genetic background
title_short Characterization and quantitative trait locus mapping of late-flowering from a Thai soybean cultivar introduced into a photoperiod-insensitive genetic background
title_sort characterization and quantitative trait locus mapping of late-flowering from a thai soybean cultivar introduced into a photoperiod-insensitive genetic background
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894811/
https://www.ncbi.nlm.nih.gov/pubmed/31805143
http://dx.doi.org/10.1371/journal.pone.0226116
work_keys_str_mv AT sunfei characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT xumeilan characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT parkcheolwoo characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT dwiyantimariastefanie characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT naganoatsushij characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT zhujianghui characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT watanabesatoshi characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT kongfanjiang characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT liubaohui characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT yamadatetsuya characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground
AT abejun characterizationandquantitativetraitlocusmappingoflatefloweringfromathaisoybeancultivarintroducedintoaphotoperiodinsensitivegeneticbackground