Flavonoid biosynthesis in four Dendrobium species based on transcriptome sequencing and metabolite analysis

Author(s):  
Yajuan Wang ◽  
Ning Jia ◽  
Peiyu Wang ◽  
Jiameng Liu ◽  
Jing Sun ◽  
...  
Forests ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 1079
Author(s):  
Lei Zhang ◽  
Gaiping Wang ◽  
Guibin Wang ◽  
Fuliang Cao

Light quality is a key environmental factor affecting plant growth and development. In this study, RNA-seq technology was used to explore the molecular mechanisms of ginkgo metabolism under different monochromatic lights. Leaves were used for transcriptome sequencing analysis after being irradiated by red, blue, and white LED lights. After treatment, 2040 differentially expressed genes (DEGs) were identified. Gene Ontology (GO) analysis showed that the DEGs were annotated into 49 terms. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that 736 DEGs were enriched in 100 metabolic pathways, and 13 metabolic pathways were significantly enriched, especially ‘phenylpropanoid biosynthesis’ and ‘flavonoid biosynthesis’. Further analysis of DEGs expression in the two pathways showed that Ginkgo biloba adapts to blue light mainly by promoting the expression of GbFLS to synthesize quercetin, kaempferol, and myncetin, and adapts to red light by promoting the expression of GbDFR to synthesize leucocyanidin. Nine DEGs were randomly selected for qRT-PCR verification, and the gene expression results were consistent with that of transcriptome sequencing. In conclusion, this study is the first to explore the molecular mechanism of ginkgo in response to different monochromatic lights, and it will lay a foundation for the research and application of light quality in the cultivation of leaf-use G. biloba.


2021 ◽  
Vol 12 ◽  
Author(s):  
Jiayi Zhu ◽  
Xueying Guo ◽  
Xin Li ◽  
Dongqin Tang

Freesia hybrida is rich in flower colors with beautiful flower shapes and pleasant aroma. Flavonoids are vital to the color formation of its flowers. In this study, five Freesia cultivars with different flower colors were used to study on the level of accumulation of their flavonoids and expression of flavonoid-related genes and further explore new novel transcription factor (TF). Ultra-high-performance liquid chromatography and VION ion mobility quadrupole time-of-flight mass spectrometer (UPLC-Q-TOF-MS) were used to determine the flavonoids. Combined with transcriptome sequencing technology, the molecular mechanism of the flavonoid metabolism difference in Freesia was revealed. A total of 10 anthoxanthin components and 12 anthocyanin components were detected using UPLC-Q-TOF-MS. All six common anthocyanin aglycones in high plants, including cyanidin, delphinidin, petunidin, peonidin, malvidin, and pelargonidin, were detected in Freesia at first time in this study. In orange, yellow, and white cultivars, anthoxanthins gradually decreased with the opening of the petals, while in red and purple cultivars, anthoxanthins first increased and then decreased. No anthocyanin was detected in yellow and white cultivars, while anthocyanins increased with the opening of the petals and reached their maximum at the flowering stage (S3) in other three cultivars. The correlation analysis revealed that the color of Freesia petals was closely related to the composition and content of anthoxanthins and anthocyanins. Petals of five cultivars at S3 were then selected for transcriptome sequencing by using the Illumina Hiseq 4000 platform, and a total of 100,539 unigenes were obtained. There were totally 5,162 differentially expressed genes (DEGs) when the four colored cultivars were compared with the white cultivar at S3. Comparing all DEGs with gene ontology (GO), KEGG, and Pfam databases, it was found that the genes involved in the flavonoid biosynthesis pathway were significantly different. In addition, AP2, WRKY, and bHLH TF families ranked the top three among all differently expressed TFs in all DEGs. Quantitative real-time PCR (qRT-PCR) technology was used to analyze the expression patterns of the structural genes of flavonoid biosynthesis pathway in Freesia. The results showed that metabolic process was affected significantly by structural genes in this pathway, such as CHS1, CHI2, DFR1, ANS1, 3GT1, and FLS1. Cluster analysis was performed by using all annotated WRKY and AP2 TFs and the above structural genes based on their relatively expression. Four novel candidate TFs of WRKY and AP2 family were screened. Their spatiotemporal expression patterns revealed that these four novel TFs may participate in the regulation of the flavonoid biosynthesis, thus controlling its color formation in Freesia petals.


2019 ◽  
Vol 63 ◽  
pp. 765-775
Author(s):  
Y.J. HAN ◽  
M.F. DONG ◽  
H.Y. WANG ◽  
X.D. WANG ◽  
K. LI ◽  
...  

2014 ◽  
Vol 65 (12) ◽  
pp. 3157-3164 ◽  
Author(s):  
Qian Lou ◽  
Yali Liu ◽  
Yinyan Qi ◽  
Shuzhen Jiao ◽  
Feifei Tian ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4836
Author(s):  
Yaqiong Wu ◽  
Tongli Wang ◽  
Yue Xin ◽  
Guibin Wang ◽  
Li-An Xu

The flavonoids in Ginkgo biloba L. (ginkgo) have important medicinal uses due to their antioxidant, antitumor, and blood circulation-promoting effects. However, the genetic mechanisms underlying flavonoid biosynthesis in ginkgo remain elusive. Flavonoid 3′, 5′-hydroxylase (F3′5′H) is an important enzyme in flavonoid synthesis. We detected a novel differentially expressed GbF3′5′H1 gene homologous to the F3′5′H enzyme involved in the flavonoid synthesis pathway through transcriptome sequencing. In this study, we characterized this gene, performed an expression analysis, and heterologously overexpressed GbF3′5′H1 in Populus. Our results showed that GbF3′5′H1 is abundant in the leaf and highly expressed during April. We also found four metabolites closely related to flavonoid biosynthesis. Importantly, the contents of 4′,5-dihydroxy-7-glucosyloxyflavanone, epicatechin, and gallocatechin were significantly higher in transgenic plants than in nontransgenic plants. Our findings revealed that the GbF3′5′H1 gene functions in the biosynthesis of flavonoid-related metabolites, suggesting that GbF3′5′H1 represents a prime candidate for future studies (e.g., gene-editing) aiming to optimize ginkgo flavonoid production, especially that of flavan-3-ols.


BMC Genomics ◽  
2016 ◽  
Vol 17 (1) ◽  
Author(s):  
Qian Wu ◽  
Jie Wu ◽  
Shan-Shan Li ◽  
Hui-Jin Zhang ◽  
Cheng-Yong Feng ◽  
...  

2017 ◽  
Vol 14 (12) ◽  
pp. e1700369 ◽  
Author(s):  
Fu-Sheng Zhang ◽  
Qian-Yu Wang ◽  
Ya-Jie Pu ◽  
Tong-Yao Chen ◽  
Xue-Mei Qin ◽  
...  

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