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Bioinformatics-based Screening of Key Genes for Saponin Metabolism in Quinoa
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Abstract
Quinoa saponins have complex, diverse and evident physiologic activities. However, the key regulatory genes for quinoa saponin metabolism are not yet well studied. The purpose of this study was to explore genes closely related to quinoa saponin metabolism. In this study, the significantly differentially expressed genes in yellow quinoa were firstly screened based on RNA-seq technology. Then, the key genes for saponin metabolism were selected by gene set enrichment analysis (GSEA) and principal component analysis (PCA) statistical methods. Finally, the specificity of the key genes was verified by hierarchical clustering. The results of differential analysis showed that 1654 differentially expressed genes were achieved after pseudogenes deletion. Therein, there were 142 long non-coding genes and 1512 protein-coding genes. Based on GSEA analysis, 116 key candidate genes were found to be significantly correlated with quinoa saponin metabolism. Through PCA dimension reduction analysis, 57 key genes were finally obtained. Hierarchical cluster analysis further demonstrated that these key genes can clearly separate the four groups of samples. The present results could provide references for the breeding of sweet quinoa and would be helpful for the rational utilization of quinoa saponins.
Title: Bioinformatics-based Screening of Key Genes for Saponin Metabolism in Quinoa
Description:
Abstract
Quinoa saponins have complex, diverse and evident physiologic activities.
However, the key regulatory genes for quinoa saponin metabolism are not yet well studied.
The purpose of this study was to explore genes closely related to quinoa saponin metabolism.
In this study, the significantly differentially expressed genes in yellow quinoa were firstly screened based on RNA-seq technology.
Then, the key genes for saponin metabolism were selected by gene set enrichment analysis (GSEA) and principal component analysis (PCA) statistical methods.
Finally, the specificity of the key genes was verified by hierarchical clustering.
The results of differential analysis showed that 1654 differentially expressed genes were achieved after pseudogenes deletion.
Therein, there were 142 long non-coding genes and 1512 protein-coding genes.
Based on GSEA analysis, 116 key candidate genes were found to be significantly correlated with quinoa saponin metabolism.
Through PCA dimension reduction analysis, 57 key genes were finally obtained.
Hierarchical cluster analysis further demonstrated that these key genes can clearly separate the four groups of samples.
The present results could provide references for the breeding of sweet quinoa and would be helpful for the rational utilization of quinoa saponins.
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Abstract
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