Evidence map›Paper›PMID 31805143›Full record

ArticlePloS one2019

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

Fei Sun, Meilan Xu, Cheolwoo Park, Maria Stefanie Dwiyanti, Atsushi J Nagano, Jianghui Zhu, Satoshi Watanabe, Fanjiang Kong, Baohui Liu, Tetsuya Yamada and 1 more

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Molecular breeding for improvement of photothermal adaptability in soybean.Molecular breeding : new strategies in plant improvement · 2023
    Article
  3. Article
  4. Rapid excavating aMolecular breeding : new strategies in plant improvement · 2021
    Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Fei SunResearch Faculty of Agriculture, Hokkaido University, Sapporo, Hokkaido, Japan.
Meilan XuResearch Faculty of Agriculture, Hokkaido University, Sapporo, Hokkaido, Japan.
Cheolwoo ParkResearch Faculty of Agriculture, Hokkaido University, Sapporo, Hokkaido, Japan.
Maria Stefanie DwiyantiResearch Faculty of Agriculture, Hokkaido University, Sapporo, Hokkaido, Japan.
Atsushi J NaganoFaculty of Agriculture, Ryukoku University, Otsu, Shiga, Japan.
Jianghui ZhuResearch Faculty of Agriculture, Hokkaido University, Sapporo, Hokkaido, Japan.
Satoshi WatanabeFaculty of Agriculture, Saga University, Saga, Saga, Japan.
Fanjiang KongSchool of Life Sciences, Guangzhou University, Guangzhou, China.
Baohui LiuSchool of Life Sciences, Guangzhou University, Guangzhou, China.
Tetsuya YamadaResearch Faculty of Agriculture, Hokkaido University, Sapporo, Hokkaido, Japan.
Jun AbeResearch Faculty of Agriculture, Hokkaido University, Sapporo, Hokkaido, Japan.ORCID 0000-0002-0856-9192

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Chromosome MappingPhotoperiodFlowersGlycine maxHot TemperatureLightLinkage DisequilibriumPlant ProteinsPolymorphism, GeneticQuantitative Trait LociPlant Proteins

Identifiers

PMID31805143
PMCPMC6894811

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.