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Structural and functional analysis of tomato sterol C22 desaturase

BACKGROUND: Sterols are structural and functional components of eukaryotic cell membranes. Plants produce a complex mixture of sterols, among which β-sitosterol, stigmasterol, campesterol, and cholesterol in some Solanaceae, are the most abundant species. Many reports have shown that the stigmastero...

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Autores principales: Gutiérrez-García, Laura, Arró, Montserrat, Altabella, Teresa, Ferrer, Albert, Boronat, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7972189/
https://www.ncbi.nlm.nih.gov/pubmed/33731007
http://dx.doi.org/10.1186/s12870-021-02898-7
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author Gutiérrez-García, Laura
Arró, Montserrat
Altabella, Teresa
Ferrer, Albert
Boronat, Albert
author_facet Gutiérrez-García, Laura
Arró, Montserrat
Altabella, Teresa
Ferrer, Albert
Boronat, Albert
author_sort Gutiérrez-García, Laura
collection PubMed
description BACKGROUND: Sterols are structural and functional components of eukaryotic cell membranes. Plants produce a complex mixture of sterols, among which β-sitosterol, stigmasterol, campesterol, and cholesterol in some Solanaceae, are the most abundant species. Many reports have shown that the stigmasterol to β-sitosterol ratio changes during plant development and in response to stresses, suggesting that it may play a role in the regulation of these processes. In tomato (Solanum lycopersicum), changes in the stigmasterol to β-sitosterol ratio correlate with the induction of the only gene encoding sterol C22-desaturase (C22DES), the enzyme specifically involved in the conversion of β-sitosterol to stigmasterol. However, despite the biological interest of this enzyme, there is still a lack of knowledge about several relevant aspects related to its structure and function. RESULTS: In this study we report the subcellular localization of tomato C22DES in the endoplasmic reticulum (ER) based on confocal fluorescence microscopy and cell fractionation analyses. Modeling studies have also revealed that C22DES consists of two well-differentiated domains: a single N-terminal transmembrane-helix domain (TMH) anchored in the ER-membrane and a globular (or catalytic) domain that is oriented towards the cytosol. Although TMH is sufficient for the targeting and retention of the enzyme in the ER, the globular domain may also interact and be retained in the ER in the absence of the N-terminal transmembrane domain. The observation that a truncated version of C22DES lacking the TMH is enzymatically inactive revealed that the N-terminal membrane domain is essential for enzyme activity. The in silico analysis of the TMH region of plant C22DES revealed several structural features that could be involved in substrate recognition and binding. CONCLUSIONS: Overall, this study contributes to expand the current knowledge on the structure and function of plant C22DES and to unveil novel aspects related to plant sterol metabolism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-02898-7.
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spelling pubmed-79721892021-03-19 Structural and functional analysis of tomato sterol C22 desaturase Gutiérrez-García, Laura Arró, Montserrat Altabella, Teresa Ferrer, Albert Boronat, Albert BMC Plant Biol Research Article BACKGROUND: Sterols are structural and functional components of eukaryotic cell membranes. Plants produce a complex mixture of sterols, among which β-sitosterol, stigmasterol, campesterol, and cholesterol in some Solanaceae, are the most abundant species. Many reports have shown that the stigmasterol to β-sitosterol ratio changes during plant development and in response to stresses, suggesting that it may play a role in the regulation of these processes. In tomato (Solanum lycopersicum), changes in the stigmasterol to β-sitosterol ratio correlate with the induction of the only gene encoding sterol C22-desaturase (C22DES), the enzyme specifically involved in the conversion of β-sitosterol to stigmasterol. However, despite the biological interest of this enzyme, there is still a lack of knowledge about several relevant aspects related to its structure and function. RESULTS: In this study we report the subcellular localization of tomato C22DES in the endoplasmic reticulum (ER) based on confocal fluorescence microscopy and cell fractionation analyses. Modeling studies have also revealed that C22DES consists of two well-differentiated domains: a single N-terminal transmembrane-helix domain (TMH) anchored in the ER-membrane and a globular (or catalytic) domain that is oriented towards the cytosol. Although TMH is sufficient for the targeting and retention of the enzyme in the ER, the globular domain may also interact and be retained in the ER in the absence of the N-terminal transmembrane domain. The observation that a truncated version of C22DES lacking the TMH is enzymatically inactive revealed that the N-terminal membrane domain is essential for enzyme activity. The in silico analysis of the TMH region of plant C22DES revealed several structural features that could be involved in substrate recognition and binding. CONCLUSIONS: Overall, this study contributes to expand the current knowledge on the structure and function of plant C22DES and to unveil novel aspects related to plant sterol metabolism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-02898-7. BioMed Central 2021-03-17 /pmc/articles/PMC7972189/ /pubmed/33731007 http://dx.doi.org/10.1186/s12870-021-02898-7 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Gutiérrez-García, Laura
Arró, Montserrat
Altabella, Teresa
Ferrer, Albert
Boronat, Albert
Structural and functional analysis of tomato sterol C22 desaturase
title Structural and functional analysis of tomato sterol C22 desaturase
title_full Structural and functional analysis of tomato sterol C22 desaturase
title_fullStr Structural and functional analysis of tomato sterol C22 desaturase
title_full_unstemmed Structural and functional analysis of tomato sterol C22 desaturase
title_short Structural and functional analysis of tomato sterol C22 desaturase
title_sort structural and functional analysis of tomato sterol c22 desaturase
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7972189/
https://www.ncbi.nlm.nih.gov/pubmed/33731007
http://dx.doi.org/10.1186/s12870-021-02898-7
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