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Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene

BACKGROUND: Valencene is a major sesquiterpene in citrus oil and biosynthesized by valencene synthase (Cstps1; EC: 4.2.3.73) from the 15-carbon substrate farnesyl diphosphate. It is abundant in juice of some mandarins (e.g. Citrus reticulata Blanco cv. Fortune), however, it is undetectable in others...

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Autores principales: Yu, Qibin, Huang, Ming, Jia, Hongge, Yu, Yuan, Plotto, Anne, Baldwin, Elizabeth A., Bai, Jinhe, Wang, Nian, Gmitter Jr, Frederick G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417135/
https://www.ncbi.nlm.nih.gov/pubmed/30866831
http://dx.doi.org/10.1186/s12870-019-1701-6
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author Yu, Qibin
Huang, Ming
Jia, Hongge
Yu, Yuan
Plotto, Anne
Baldwin, Elizabeth A.
Bai, Jinhe
Wang, Nian
Gmitter Jr, Frederick G.
author_facet Yu, Qibin
Huang, Ming
Jia, Hongge
Yu, Yuan
Plotto, Anne
Baldwin, Elizabeth A.
Bai, Jinhe
Wang, Nian
Gmitter Jr, Frederick G.
author_sort Yu, Qibin
collection PubMed
description BACKGROUND: Valencene is a major sesquiterpene in citrus oil and biosynthesized by valencene synthase (Cstps1; EC: 4.2.3.73) from the 15-carbon substrate farnesyl diphosphate. It is abundant in juice of some mandarins (e.g. Citrus reticulata Blanco cv. Fortune), however, it is undetectable in others (e.g. C. reticulata Blanco cv. Murcott), We have discovered that the Murcott mandarin Cstps1 gene expression is severely reduced. A previous genetic mapping study using an F1 population of Fortune × Murcott found that the segregation of valencene production in fruit exhibited a Mendelian inheritance ratio of 1:1. There was only one dominant locus associated with valencene content detected on the mandarin genetic map. The goal of this study was to understand the molecular mechanism underlying the valencene deficiency observed in some citrus hybrids. RESULTS: There was a clear relationship between presence or absence of the valencene synthase gene (Cstps1) expression, and presence or absence of valencene among randomly selected mandarin hybrids. Cloning the coding regions of Cstps1 from Fortune and Murcott mandarin, and aligning with previous reported Valencia orange Cstps1 sequence, showed that they both exhibited extremely high similarity with the known Cstps1. By further cloning and analyzing the promoter region of Cstps1 from Valencia, Fortune and Murcott, a 12-nucleotide deletion at approximately − 270 bp from the Cstps1 coding region was only found in Murcott. Three binary vectors, designated as p1380-FortP-GUSin, p1380-MurcP-GUSin and p1380-MurcP(+ 12)-GUSin, were developed for promoter activity analysis. Transient over-expression of Fortune Cstps1 promoter in sweet orange showed notable GUS activity, but the Murcott Cstps1 promoter did not. In addition, by re-inserting the 12-nucleotide fragment, the activity of the Murcott Cstps1 promoter was mostly recovered. CONCLUSION: The deficiency of valencene production in some mandarins is probably due to a 12-nucleotide deletion in the promoter region of the Cstps1, which could be a crucial switch of Cstps1 transcription. Our results further enhanced the understanding of valencene biosynthesis in citrus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1701-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-64171352019-03-25 Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene Yu, Qibin Huang, Ming Jia, Hongge Yu, Yuan Plotto, Anne Baldwin, Elizabeth A. Bai, Jinhe Wang, Nian Gmitter Jr, Frederick G. BMC Plant Biol Research Article BACKGROUND: Valencene is a major sesquiterpene in citrus oil and biosynthesized by valencene synthase (Cstps1; EC: 4.2.3.73) from the 15-carbon substrate farnesyl diphosphate. It is abundant in juice of some mandarins (e.g. Citrus reticulata Blanco cv. Fortune), however, it is undetectable in others (e.g. C. reticulata Blanco cv. Murcott), We have discovered that the Murcott mandarin Cstps1 gene expression is severely reduced. A previous genetic mapping study using an F1 population of Fortune × Murcott found that the segregation of valencene production in fruit exhibited a Mendelian inheritance ratio of 1:1. There was only one dominant locus associated with valencene content detected on the mandarin genetic map. The goal of this study was to understand the molecular mechanism underlying the valencene deficiency observed in some citrus hybrids. RESULTS: There was a clear relationship between presence or absence of the valencene synthase gene (Cstps1) expression, and presence or absence of valencene among randomly selected mandarin hybrids. Cloning the coding regions of Cstps1 from Fortune and Murcott mandarin, and aligning with previous reported Valencia orange Cstps1 sequence, showed that they both exhibited extremely high similarity with the known Cstps1. By further cloning and analyzing the promoter region of Cstps1 from Valencia, Fortune and Murcott, a 12-nucleotide deletion at approximately − 270 bp from the Cstps1 coding region was only found in Murcott. Three binary vectors, designated as p1380-FortP-GUSin, p1380-MurcP-GUSin and p1380-MurcP(+ 12)-GUSin, were developed for promoter activity analysis. Transient over-expression of Fortune Cstps1 promoter in sweet orange showed notable GUS activity, but the Murcott Cstps1 promoter did not. In addition, by re-inserting the 12-nucleotide fragment, the activity of the Murcott Cstps1 promoter was mostly recovered. CONCLUSION: The deficiency of valencene production in some mandarins is probably due to a 12-nucleotide deletion in the promoter region of the Cstps1, which could be a crucial switch of Cstps1 transcription. Our results further enhanced the understanding of valencene biosynthesis in citrus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1701-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-13 /pmc/articles/PMC6417135/ /pubmed/30866831 http://dx.doi.org/10.1186/s12870-019-1701-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Yu, Qibin
Huang, Ming
Jia, Hongge
Yu, Yuan
Plotto, Anne
Baldwin, Elizabeth A.
Bai, Jinhe
Wang, Nian
Gmitter Jr, Frederick G.
Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene
title Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene
title_full Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene
title_fullStr Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene
title_full_unstemmed Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene
title_short Deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene
title_sort deficiency of valencene in mandarin hybrids is associated with a deletion in the promoter region of the valencene synthase gene
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417135/
https://www.ncbi.nlm.nih.gov/pubmed/30866831
http://dx.doi.org/10.1186/s12870-019-1701-6
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