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Specialized metabolism by trichome-enriched Rubisco and fatty acid synthase components
Acylsugars, specialized metabolites with defense activities, are secreted by trichomes of many solanaceous plants. Several acylsugar metabolic genes (AMGs) remain unknown. We previously reported multiple candidate AMGs. Here, using multiple approaches, we characterized additional AMGs. First, we ide...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922422/ https://www.ncbi.nlm.nih.gov/pubmed/36264116 http://dx.doi.org/10.1093/plphys/kiac487 |
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author | Ji, Wangming Mandal, Sabyasachi Rezenom, Yohannes H McKnight, Thomas D |
author_facet | Ji, Wangming Mandal, Sabyasachi Rezenom, Yohannes H McKnight, Thomas D |
author_sort | Ji, Wangming |
collection | PubMed |
description | Acylsugars, specialized metabolites with defense activities, are secreted by trichomes of many solanaceous plants. Several acylsugar metabolic genes (AMGs) remain unknown. We previously reported multiple candidate AMGs. Here, using multiple approaches, we characterized additional AMGs. First, we identified differentially expressed genes between high- and low-acylsugar-producing F(2) plants derived from a cross between cultivated tomato (Solanum lycopersicum) and a wild relative (Solanum pennellii), which produce acylsugars that are ∼1% and ∼20% of leaf dry weight, respectively. Expression levels of many known and candidate AMGs positively correlated with acylsugar amounts in F(2) individuals. Next, we identified lycopersicum-pennellii putative orthologs with higher nonsynonymous to synonymous substitutions. These analyses identified four candidate genes, three of which showed enriched expression in stem trichomes compared to underlying tissues (shaved stems). Virus-induced gene silencing confirmed two candidates, Sopen05g009610 [beta-ketoacyl-(acyl-carrier-protein) reductase; fatty acid synthase component] and Sopen07g006810 (Rubisco small subunit), as AMGs. Phylogenetic analysis indicated that Sopen05g009610 is distinct from specialized metabolic cytosolic reductases but closely related to two capsaicinoid biosynthetic reductases, suggesting evolutionary relationship between acylsugar and capsaicinoid biosynthesis. Analysis of publicly available datasets revealed enriched expression of Sopen05g009610 orthologs in trichomes of several acylsugar-producing species. Similarly, orthologs of Sopen07g006810 were identified as solanaceous trichome-enriched members, which form a phylogenetic clade distinct from those of mesophyll-expressed “regular” Rubisco small subunits. Furthermore, δ(13)C analyses indicated recycling of metabolic CO(2) into acylsugars by Sopen07g006810 and showed how trichomes support high levels of specialized metabolite production. These findings have implications for genetic manipulation of trichome-specialized metabolism in solanaceous crops. |
format | Online Article Text |
id | pubmed-9922422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99224222023-02-13 Specialized metabolism by trichome-enriched Rubisco and fatty acid synthase components Ji, Wangming Mandal, Sabyasachi Rezenom, Yohannes H McKnight, Thomas D Plant Physiol Research Article Acylsugars, specialized metabolites with defense activities, are secreted by trichomes of many solanaceous plants. Several acylsugar metabolic genes (AMGs) remain unknown. We previously reported multiple candidate AMGs. Here, using multiple approaches, we characterized additional AMGs. First, we identified differentially expressed genes between high- and low-acylsugar-producing F(2) plants derived from a cross between cultivated tomato (Solanum lycopersicum) and a wild relative (Solanum pennellii), which produce acylsugars that are ∼1% and ∼20% of leaf dry weight, respectively. Expression levels of many known and candidate AMGs positively correlated with acylsugar amounts in F(2) individuals. Next, we identified lycopersicum-pennellii putative orthologs with higher nonsynonymous to synonymous substitutions. These analyses identified four candidate genes, three of which showed enriched expression in stem trichomes compared to underlying tissues (shaved stems). Virus-induced gene silencing confirmed two candidates, Sopen05g009610 [beta-ketoacyl-(acyl-carrier-protein) reductase; fatty acid synthase component] and Sopen07g006810 (Rubisco small subunit), as AMGs. Phylogenetic analysis indicated that Sopen05g009610 is distinct from specialized metabolic cytosolic reductases but closely related to two capsaicinoid biosynthetic reductases, suggesting evolutionary relationship between acylsugar and capsaicinoid biosynthesis. Analysis of publicly available datasets revealed enriched expression of Sopen05g009610 orthologs in trichomes of several acylsugar-producing species. Similarly, orthologs of Sopen07g006810 were identified as solanaceous trichome-enriched members, which form a phylogenetic clade distinct from those of mesophyll-expressed “regular” Rubisco small subunits. Furthermore, δ(13)C analyses indicated recycling of metabolic CO(2) into acylsugars by Sopen07g006810 and showed how trichomes support high levels of specialized metabolite production. These findings have implications for genetic manipulation of trichome-specialized metabolism in solanaceous crops. Oxford University Press 2022-10-20 /pmc/articles/PMC9922422/ /pubmed/36264116 http://dx.doi.org/10.1093/plphys/kiac487 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Ji, Wangming Mandal, Sabyasachi Rezenom, Yohannes H McKnight, Thomas D Specialized metabolism by trichome-enriched Rubisco and fatty acid synthase components |
title | Specialized metabolism by trichome-enriched Rubisco and fatty acid synthase components |
title_full | Specialized metabolism by trichome-enriched Rubisco and fatty acid synthase components |
title_fullStr | Specialized metabolism by trichome-enriched Rubisco and fatty acid synthase components |
title_full_unstemmed | Specialized metabolism by trichome-enriched Rubisco and fatty acid synthase components |
title_short | Specialized metabolism by trichome-enriched Rubisco and fatty acid synthase components |
title_sort | specialized metabolism by trichome-enriched rubisco and fatty acid synthase components |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922422/ https://www.ncbi.nlm.nih.gov/pubmed/36264116 http://dx.doi.org/10.1093/plphys/kiac487 |
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