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Brassica rapa orphan genes largely affect soluble sugar metabolism

Orphan genes (OGs), which are genes unique to a specific taxon, play a vital role in primary metabolism. However, little is known about the functional significance of Brassica rapa OGs (BrOGs) that were identified in our previous study. To study their biological functions, we developed a BrOG overex...

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Autores principales: Jiang, Mingliang, Zhan, Zongxiang, Li, Haiyan, Dong, Xiangshu, Cheng, Feng, Piao, Zhongyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603504/
https://www.ncbi.nlm.nih.gov/pubmed/33328469
http://dx.doi.org/10.1038/s41438-020-00403-z
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author Jiang, Mingliang
Zhan, Zongxiang
Li, Haiyan
Dong, Xiangshu
Cheng, Feng
Piao, Zhongyun
author_facet Jiang, Mingliang
Zhan, Zongxiang
Li, Haiyan
Dong, Xiangshu
Cheng, Feng
Piao, Zhongyun
author_sort Jiang, Mingliang
collection PubMed
description Orphan genes (OGs), which are genes unique to a specific taxon, play a vital role in primary metabolism. However, little is known about the functional significance of Brassica rapa OGs (BrOGs) that were identified in our previous study. To study their biological functions, we developed a BrOG overexpression (BrOGOE) mutant library of 43 genes in Arabidopsis thaliana and assessed the phenotypic variation of the plants. We found that 19 of the 43 BrOGOE mutants displayed a mutant phenotype and 42 showed a variable soluble sugar content. One mutant, BrOG1OE, with significantly elevated fructose, glucose, and total sugar contents but a reduced sucrose content, was selected for in-depth analysis. BrOG1OE showed reduced expression and activity of the Arabidopsis sucrose synthase gene (AtSUS); however, the activity of invertase was unchanged. In contrast, silencing of two copies of BrOG1 in B. rapa, BraA08002322 (BrOG1A) and BraSca000221 (BrOG1B), by the use of an efficient CRISPR/Cas9 system of Chinese cabbage (B. rapa ssp. campestris) resulted in decreased fructose, glucose, and total soluble sugar contents because of the upregulation of BrSUS1b, BrSUS3, and, specifically, the BrSUS5 gene in the edited BrOG1 transgenic line. In addition, we observed increased sucrose content and SUS activity in the BrOG1 mutants, with the activity of invertase remaining unchanged. Thus, BrOG1 probably affected soluble sugar metabolism in a SUS-dependent manner. This is the first report investigating the function of BrOGs with respect to soluble sugar metabolism and reinforced the idea that OGs are a valuable resource for nutrient metabolism.
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spelling pubmed-76035042020-11-02 Brassica rapa orphan genes largely affect soluble sugar metabolism Jiang, Mingliang Zhan, Zongxiang Li, Haiyan Dong, Xiangshu Cheng, Feng Piao, Zhongyun Hortic Res Article Orphan genes (OGs), which are genes unique to a specific taxon, play a vital role in primary metabolism. However, little is known about the functional significance of Brassica rapa OGs (BrOGs) that were identified in our previous study. To study their biological functions, we developed a BrOG overexpression (BrOGOE) mutant library of 43 genes in Arabidopsis thaliana and assessed the phenotypic variation of the plants. We found that 19 of the 43 BrOGOE mutants displayed a mutant phenotype and 42 showed a variable soluble sugar content. One mutant, BrOG1OE, with significantly elevated fructose, glucose, and total sugar contents but a reduced sucrose content, was selected for in-depth analysis. BrOG1OE showed reduced expression and activity of the Arabidopsis sucrose synthase gene (AtSUS); however, the activity of invertase was unchanged. In contrast, silencing of two copies of BrOG1 in B. rapa, BraA08002322 (BrOG1A) and BraSca000221 (BrOG1B), by the use of an efficient CRISPR/Cas9 system of Chinese cabbage (B. rapa ssp. campestris) resulted in decreased fructose, glucose, and total soluble sugar contents because of the upregulation of BrSUS1b, BrSUS3, and, specifically, the BrSUS5 gene in the edited BrOG1 transgenic line. In addition, we observed increased sucrose content and SUS activity in the BrOG1 mutants, with the activity of invertase remaining unchanged. Thus, BrOG1 probably affected soluble sugar metabolism in a SUS-dependent manner. This is the first report investigating the function of BrOGs with respect to soluble sugar metabolism and reinforced the idea that OGs are a valuable resource for nutrient metabolism. Nature Publishing Group UK 2020-11-01 /pmc/articles/PMC7603504/ /pubmed/33328469 http://dx.doi.org/10.1038/s41438-020-00403-z 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jiang, Mingliang
Zhan, Zongxiang
Li, Haiyan
Dong, Xiangshu
Cheng, Feng
Piao, Zhongyun
Brassica rapa orphan genes largely affect soluble sugar metabolism
title Brassica rapa orphan genes largely affect soluble sugar metabolism
title_full Brassica rapa orphan genes largely affect soluble sugar metabolism
title_fullStr Brassica rapa orphan genes largely affect soluble sugar metabolism
title_full_unstemmed Brassica rapa orphan genes largely affect soluble sugar metabolism
title_short Brassica rapa orphan genes largely affect soluble sugar metabolism
title_sort brassica rapa orphan genes largely affect soluble sugar metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603504/
https://www.ncbi.nlm.nih.gov/pubmed/33328469
http://dx.doi.org/10.1038/s41438-020-00403-z
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