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Molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (Manihot esculenta Crantz)

Sucrose phosphate synthase (SPS), a key rate-limiting enzyme in the sucrose biosynthesis pathway in plants, is encoded by a multi-gene family. Until recently, the identification and characterization of the SPS gene family have been performed for dozens of plant species; however, few studies have inv...

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Autores principales: Huang, Tangwei, Luo, Xinglu, Wei, Maogui, Shan, Zhongying, Zhu, Yanmei, Yang, Yanni, Fan, Zhupeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692556/
https://www.ncbi.nlm.nih.gov/pubmed/33244128
http://dx.doi.org/10.1038/s41598-020-77669-9
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author Huang, Tangwei
Luo, Xinglu
Wei, Maogui
Shan, Zhongying
Zhu, Yanmei
Yang, Yanni
Fan, Zhupeng
author_facet Huang, Tangwei
Luo, Xinglu
Wei, Maogui
Shan, Zhongying
Zhu, Yanmei
Yang, Yanni
Fan, Zhupeng
author_sort Huang, Tangwei
collection PubMed
description Sucrose phosphate synthase (SPS), a key rate-limiting enzyme in the sucrose biosynthesis pathway in plants, is encoded by a multi-gene family. Until recently, the identification and characterization of the SPS gene family have been performed for dozens of plant species; however, few studies have involved a comprehensive analysis of the SPS family members in tropical crops, such as cassava (Manihot esculenta Crantz). In the current study, five SPS genes (MeSPS1, MeSPS2, MeSPS3, MeSPS4, and MeSPS5) were isolated from cassava, and their sequence characteristics were comprehensively characterized. These MeSPS genes were found distributed on five chromosomes (Chr2, Chr14, Chr15, Chr16, and Chr18). Phylogenetic analysis showed that the MeSPS protein sequences were clustered into three families, together with other SPS sequences from both dicot and monocot species (families A, B, and C). The spatio-temporal expression pattern analysis of MeSPS genes showed a tissue-specific and partially overlapping expression pattern, with the genes mainly expressed in source tissues during cassava growth and development. Correlation analysis revealed that the expression of MeSPS genes correlated positively with root starch content, indicating that the expression of MeSPS genes might accelerate the rate of starch accumulation in the roots of cassava plants.
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spelling pubmed-76925562020-11-30 Molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (Manihot esculenta Crantz) Huang, Tangwei Luo, Xinglu Wei, Maogui Shan, Zhongying Zhu, Yanmei Yang, Yanni Fan, Zhupeng Sci Rep Article Sucrose phosphate synthase (SPS), a key rate-limiting enzyme in the sucrose biosynthesis pathway in plants, is encoded by a multi-gene family. Until recently, the identification and characterization of the SPS gene family have been performed for dozens of plant species; however, few studies have involved a comprehensive analysis of the SPS family members in tropical crops, such as cassava (Manihot esculenta Crantz). In the current study, five SPS genes (MeSPS1, MeSPS2, MeSPS3, MeSPS4, and MeSPS5) were isolated from cassava, and their sequence characteristics were comprehensively characterized. These MeSPS genes were found distributed on five chromosomes (Chr2, Chr14, Chr15, Chr16, and Chr18). Phylogenetic analysis showed that the MeSPS protein sequences were clustered into three families, together with other SPS sequences from both dicot and monocot species (families A, B, and C). The spatio-temporal expression pattern analysis of MeSPS genes showed a tissue-specific and partially overlapping expression pattern, with the genes mainly expressed in source tissues during cassava growth and development. Correlation analysis revealed that the expression of MeSPS genes correlated positively with root starch content, indicating that the expression of MeSPS genes might accelerate the rate of starch accumulation in the roots of cassava plants. Nature Publishing Group UK 2020-11-26 /pmc/articles/PMC7692556/ /pubmed/33244128 http://dx.doi.org/10.1038/s41598-020-77669-9 Text en © The Author(s) 2020 Open Access This 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 Article
Huang, Tangwei
Luo, Xinglu
Wei, Maogui
Shan, Zhongying
Zhu, Yanmei
Yang, Yanni
Fan, Zhupeng
Molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (Manihot esculenta Crantz)
title Molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (Manihot esculenta Crantz)
title_full Molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (Manihot esculenta Crantz)
title_fullStr Molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (Manihot esculenta Crantz)
title_full_unstemmed Molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (Manihot esculenta Crantz)
title_short Molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (Manihot esculenta Crantz)
title_sort molecular cloning and expression analysis of sucrose phosphate synthase genes in cassava (manihot esculenta crantz)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692556/
https://www.ncbi.nlm.nih.gov/pubmed/33244128
http://dx.doi.org/10.1038/s41598-020-77669-9
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