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Are sesquiterpene lactones the elusive KARRIKIN-INSENSITIVE2 ligand?

MAIN CONCLUSION: The sunflower sesquiterpene lactones 8-epixanthatin and tomentosin can bind to the hydrophobic pocket of sunflower KAI2 with an affinity much higher than for the exogenous ligand KAR. ABSTRACT: Sesquiterpene lactones (STLs) are secondary plant metabolites with a wide range of biolog...

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Autores principales: Rahimi, Mehran, Bouwmeester, Harro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847861/
https://www.ncbi.nlm.nih.gov/pubmed/33521891
http://dx.doi.org/10.1007/s00425-021-03571-x
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author Rahimi, Mehran
Bouwmeester, Harro
author_facet Rahimi, Mehran
Bouwmeester, Harro
author_sort Rahimi, Mehran
collection PubMed
description MAIN CONCLUSION: The sunflower sesquiterpene lactones 8-epixanthatin and tomentosin can bind to the hydrophobic pocket of sunflower KAI2 with an affinity much higher than for the exogenous ligand KAR. ABSTRACT: Sesquiterpene lactones (STLs) are secondary plant metabolites with a wide range of biological, such as anti-microbial, activities. Intriguingly, the STLs have also been implicated in plant development: in several Asteraceae, STL levels correlate with the photo-inhibition of hypocotyl elongation. Although this effect was suggested to be due to auxin transport inhibition, there is no structural–functional evidence for this claim. Intriguingly, the light-induced inhibition of hypocotyl elongation in Arabidopsis has been ascribed to HYPOSENSITIVE TO LIGHT/KARRIKIN-INSENSITIVE2 (HTL/KAI2) signaling. KAI2 was discovered because of its affinity to the smoke-derived karrikin (KAR), though it is generally assumed that KAI2 has another, endogenous but so far elusive, ligand rather than the exogenous KARs. Here, we postulate that the effect of STLs on hypocotyl elongation is mediated through KAI2 signaling. To support this hypothesis, we have generated homology models of the sunflower KAI2s (HaKAI2s) and used them for molecular docking studies with STLs. Our results show that particularly two sunflower STLs, 8-epixanthatin and tomentosin, can bind to the hydrophobic pockets of HaKAI2s with high affinity. Our results are in line with a recent study, showing that these two STLs accumulate in the light-exposed hypocotyls of sunflower. This finding sheds light on the effect of STLs in hypocotyl elongation that has been reported for many decades but without conclusive insight in the elusive mechanism underlying this effect.
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spelling pubmed-78478612021-02-08 Are sesquiterpene lactones the elusive KARRIKIN-INSENSITIVE2 ligand? Rahimi, Mehran Bouwmeester, Harro Planta Commentary MAIN CONCLUSION: The sunflower sesquiterpene lactones 8-epixanthatin and tomentosin can bind to the hydrophobic pocket of sunflower KAI2 with an affinity much higher than for the exogenous ligand KAR. ABSTRACT: Sesquiterpene lactones (STLs) are secondary plant metabolites with a wide range of biological, such as anti-microbial, activities. Intriguingly, the STLs have also been implicated in plant development: in several Asteraceae, STL levels correlate with the photo-inhibition of hypocotyl elongation. Although this effect was suggested to be due to auxin transport inhibition, there is no structural–functional evidence for this claim. Intriguingly, the light-induced inhibition of hypocotyl elongation in Arabidopsis has been ascribed to HYPOSENSITIVE TO LIGHT/KARRIKIN-INSENSITIVE2 (HTL/KAI2) signaling. KAI2 was discovered because of its affinity to the smoke-derived karrikin (KAR), though it is generally assumed that KAI2 has another, endogenous but so far elusive, ligand rather than the exogenous KARs. Here, we postulate that the effect of STLs on hypocotyl elongation is mediated through KAI2 signaling. To support this hypothesis, we have generated homology models of the sunflower KAI2s (HaKAI2s) and used them for molecular docking studies with STLs. Our results show that particularly two sunflower STLs, 8-epixanthatin and tomentosin, can bind to the hydrophobic pockets of HaKAI2s with high affinity. Our results are in line with a recent study, showing that these two STLs accumulate in the light-exposed hypocotyls of sunflower. This finding sheds light on the effect of STLs in hypocotyl elongation that has been reported for many decades but without conclusive insight in the elusive mechanism underlying this effect. Springer Berlin Heidelberg 2021-02-01 2021 /pmc/articles/PMC7847861/ /pubmed/33521891 http://dx.doi.org/10.1007/s00425-021-03571-x Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Commentary
Rahimi, Mehran
Bouwmeester, Harro
Are sesquiterpene lactones the elusive KARRIKIN-INSENSITIVE2 ligand?
title Are sesquiterpene lactones the elusive KARRIKIN-INSENSITIVE2 ligand?
title_full Are sesquiterpene lactones the elusive KARRIKIN-INSENSITIVE2 ligand?
title_fullStr Are sesquiterpene lactones the elusive KARRIKIN-INSENSITIVE2 ligand?
title_full_unstemmed Are sesquiterpene lactones the elusive KARRIKIN-INSENSITIVE2 ligand?
title_short Are sesquiterpene lactones the elusive KARRIKIN-INSENSITIVE2 ligand?
title_sort are sesquiterpene lactones the elusive karrikin-insensitive2 ligand?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847861/
https://www.ncbi.nlm.nih.gov/pubmed/33521891
http://dx.doi.org/10.1007/s00425-021-03571-x
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