Evidence map›Paper›PMID 33370251›Full record

ArticlePLoS genetics2020

Lotus japonicus karrikin receptors display divergent ligand-binding specificities and organ-dependent redundancy.

Samy Carbonnel, Salar Torabi, Maximilian Griesmann, Elias Bleek, Yuhong Tang, Stefan Buchka, Veronica Basso, Mitsuru Shindo, François-Didier Boyer, Trevor L Wang and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.2field-weighted citation impact, top 3% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

20 citing papers in PubMed, 43 citations in OpenAlex.

  1. Negative feedback regulation of karrikin signaling inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Review
  4. An N-terminal domain specifies developmental control by the SMAX1-LIKE family of transcriptional regulators inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Article
  7. Evolution of small molecule-mediated regulation of arbuscular mycorrhiza symbiosis.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  8. Article
  9. Article
  10. Strigolactones: diversity, perception, and hydrolysis.Phytochemistry reviews : proceedings of the Phytochemical Society of Europe · 2023
    Article
  11. Article
  12. KARRIKIN UP-REGULATED F-BOX 1 (KUF1) imposes negative feedback regulation of karrikin and KAI2 ligand metabolism inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Article
  15. Review
  16. Three mutations repurpose a plant karrikin receptor to a strigolactone receptor.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Review
  18. Article
  19. Plant signaling & behavior · 2021
    Article
  20. 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

13 authors at 7 institutions in 6 countries.

Samy CarbonnelLMU Munich, Faculty of Biology, Genetics, Biocenter Martinsried, Martinsried, Germany.ORCID 0000-0003-2564-7161
Salar TorabiLMU Munich, Faculty of Biology, Genetics, Biocenter Martinsried, Martinsried, Germany.ORCID 0000-0001-7561-7716
Maximilian GriesmannLMU Munich, Faculty of Biology, Genetics, Biocenter Martinsried, Martinsried, Germany.ORCID 0000-0001-9122-4349
Elias BleekLMU Munich, Faculty of Biology, Genetics, Biocenter Martinsried, Martinsried, Germany.
Yuhong TangNoble Research Institute, Ardmore, Oklahoma, United States of America.
Stefan BuchkaLMU Munich, Faculty of Biology, Genetics, Biocenter Martinsried, Martinsried, Germany.
Veronica BassoLMU Munich, Faculty of Biology, Genetics, Biocenter Martinsried, Martinsried, Germany.ORCID 0000-0003-3273-1492
Mitsuru ShindoInstitute for Materials Chemistry and Engineering, Kyushu University, Kasuga, Fukuoka, Japan.ORCID 0000-0002-0588-8075
François-Didier BoyerUniversité Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, Gif-sur-Yvette, France.ORCID 0000-0001-9855-7234
Trevor L WangJohn Innes Centre, Norwich Research Park, Norwich, United Kingdom.
Michael UdvardiNoble Research Institute, Ardmore, Oklahoma, United States of America.
Mark T WatersSchool of Molecular Sciences, The University of Western Australia, Perth, Australia.
Caroline GutjahrLMU Munich, Faculty of Biology, Genetics, Biocenter Martinsried, Martinsried, Germany.ORCID 0000-0001-6163-745X
Ludwig-Maximilians-Universität München · DETechnical University of Munich · DENoble Research Institute · USCentre National de la Recherche Scientifique · FRJohn Innes Centre · GBKyushu University · JPThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Karrikins (KARs), smoke-derived butenolides, are perceived by the α/β-fold hydrolase KARRIKIN INSENSITIVE2 (KAI2) and thought to mimic endogenous, yet elusive plant hormones tentatively called KAI2-ligands (KLs). The sensitivity to different karrikin types as well as the number of KAI2 paralogs varies among plant species, suggesting diversification and co-evolution of ligand-receptor relationships. We found that the genomes of legumes, comprising a number of important crops with protein-rich, nutritious seed, contain two or more KAI2 copies. We uncover sub-functionalization of the two KAI2 versions in the model legume Lotus japonicus and demonstrate differences in their ability to bind the synthetic ligand GR24ent-5DS in vitro and in genetic assays with Lotus japonicus and the heterologous Arabidopsis thaliana background. These differences can be explained by the exchange of a widely conserved phenylalanine in the binding pocket of KAI2a with a tryptophan in KAI2b, which arose independently in KAI2 proteins of several unrelated angiosperms. Furthermore, two polymorphic residues in the binding pocket are conserved across a number of legumes and may contribute to ligand binding preferences. The diversification of KAI2 binding pockets suggests the occurrence of several different KLs acting in non-fire following plants, or an escape from possible antagonistic exogenous molecules. Unexpectedly, L. japonicus responds to diverse synthetic KAI2-ligands in an organ-specific manner. Hypocotyl growth responds to KAR1, KAR2 and rac-GR24, while root system development responds only to KAR1. This differential responsiveness cannot be explained by receptor-ligand preferences alone, because LjKAI2a is sufficient for karrikin responses in the hypocotyl, while LjKAI2a and LjKAI2b operate redundantly in roots. Instead, it likely reflects differences between plant organs in their ability to transport or metabolise the synthetic KLs. Our findings provide new insights into the evolution and diversity of butenolide ligand-receptor relationships, and open novel research avenues into their ecological significance and the mechanisms controlling developmental responses to divergent KLs.

Indexed as

ArabidopsisArabidopsis ProteinsFuransGene DuplicationGene Expression Regulation, PlantHeterocyclic Compounds, 3-RingHydrolasesHypocotylLactonesLigandsLotusMicroarray AnalysisPhylogenyPlant Growth RegulatorsPlant RootsPyrans3-methyl-2H-furo(2,3-c)pyran-2-oneArabidopsis ProteinsFuransGR24 strigolactoneHeterocyclic Compounds, 3-RingHTL protein, ArabidopsisHydrolasesLactonesLigandsPlant Growth RegulatorsPyrans

Identifiers

PMID33370251
PMCPMC7808659
OpenAlexW3100912694

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.