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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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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. |
format | Online Article Text |
id | pubmed-7972189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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