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It happened again: Convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato

Plants synthesize myriad phylogenetically restricted specialized (aka “secondary”) metabolites with diverse structures. Metabolism of acylated sugar esters in epidermal glandular secreting trichomes across the Solanaceae (nightshade) family is ideal for investigating the mechanisms of evolutionary m...

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Autores principales: Lou, Yann-Ru, Anthony, Thilani M., Fiesel, Paul D., Arking, Rachel E., Christensen, Elizabeth M., Jones, A. Daniel, Last, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580325/
https://www.ncbi.nlm.nih.gov/pubmed/34757799
http://dx.doi.org/10.1126/sciadv.abj8726
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author Lou, Yann-Ru
Anthony, Thilani M.
Fiesel, Paul D.
Arking, Rachel E.
Christensen, Elizabeth M.
Jones, A. Daniel
Last, Robert L.
author_facet Lou, Yann-Ru
Anthony, Thilani M.
Fiesel, Paul D.
Arking, Rachel E.
Christensen, Elizabeth M.
Jones, A. Daniel
Last, Robert L.
author_sort Lou, Yann-Ru
collection PubMed
description Plants synthesize myriad phylogenetically restricted specialized (aka “secondary”) metabolites with diverse structures. Metabolism of acylated sugar esters in epidermal glandular secreting trichomes across the Solanaceae (nightshade) family is ideal for investigating the mechanisms of evolutionary metabolic diversification. We developed methods to structurally analyze acylhexose mixtures by 2D NMR, which led to the insight that the Old World species black nightshade (Solanum nigrum) accumulates acylglucoses and acylinositols in the same tissue. Detailed in vitro biochemistry, cross-validated by in vivo virus-induced gene silencing, revealed two unique features of the four-step acylglucose biosynthetic pathway: A trichome-expressed, neofunctionalized invertase-like enzyme, SnASFF1, converts BAHD-produced acylsucroses to acylglucoses, which, in turn, are substrates for the acylglucose acyltransferase, SnAGAT1. This biosynthetic pathway evolved independently from that recently described in the wild tomato Solanum pennellii, reinforcing that acylsugar biosynthesis is evolutionarily dynamic with independent examples of primary metabolic enzyme cooption and additional variation in BAHD acyltransferases.
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spelling pubmed-85803252021-11-18 It happened again: Convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato Lou, Yann-Ru Anthony, Thilani M. Fiesel, Paul D. Arking, Rachel E. Christensen, Elizabeth M. Jones, A. Daniel Last, Robert L. Sci Adv Biomedicine and Life Sciences Plants synthesize myriad phylogenetically restricted specialized (aka “secondary”) metabolites with diverse structures. Metabolism of acylated sugar esters in epidermal glandular secreting trichomes across the Solanaceae (nightshade) family is ideal for investigating the mechanisms of evolutionary metabolic diversification. We developed methods to structurally analyze acylhexose mixtures by 2D NMR, which led to the insight that the Old World species black nightshade (Solanum nigrum) accumulates acylglucoses and acylinositols in the same tissue. Detailed in vitro biochemistry, cross-validated by in vivo virus-induced gene silencing, revealed two unique features of the four-step acylglucose biosynthetic pathway: A trichome-expressed, neofunctionalized invertase-like enzyme, SnASFF1, converts BAHD-produced acylsucroses to acylglucoses, which, in turn, are substrates for the acylglucose acyltransferase, SnAGAT1. This biosynthetic pathway evolved independently from that recently described in the wild tomato Solanum pennellii, reinforcing that acylsugar biosynthesis is evolutionarily dynamic with independent examples of primary metabolic enzyme cooption and additional variation in BAHD acyltransferases. American Association for the Advancement of Science 2021-11-10 /pmc/articles/PMC8580325/ /pubmed/34757799 http://dx.doi.org/10.1126/sciadv.abj8726 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Lou, Yann-Ru
Anthony, Thilani M.
Fiesel, Paul D.
Arking, Rachel E.
Christensen, Elizabeth M.
Jones, A. Daniel
Last, Robert L.
It happened again: Convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato
title It happened again: Convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato
title_full It happened again: Convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato
title_fullStr It happened again: Convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato
title_full_unstemmed It happened again: Convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato
title_short It happened again: Convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato
title_sort it happened again: convergent evolution of acylglucose specialized metabolism in black nightshade and wild tomato
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580325/
https://www.ncbi.nlm.nih.gov/pubmed/34757799
http://dx.doi.org/10.1126/sciadv.abj8726
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