Qi Sheng’s research while affiliated with Guizhou University and other places

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Publications (2)


Bioinformatics analysis of tea plant CsBRC. (a) Phylogenetic analysis of CsBRC. (b) Protein alignment of homologous sequences. The conserved domain of CsBRC is indicated by the black line.
Subcellular localization of CsBRC in tobacco leaves. Note: Left to right are fluorescence channel, brightfield, and superposition field.
Phenotypic characterization of CsBRC‐transgenic plants. (a) Phenotypes of transgenic “K326” tobacco (OXCsBRC) and WT. (b) The number of flower buds of transgenic “K326” tobacco (OXCsBRC) and WT. (c) Phenotypic comparison of transgenic N. benthamiana (35S::CsBRC) and WT. (d) Branching phenotype of WT. (e) Branching phenotype of transgenic N. benthamiana (35S::CsBRC). (f) Branch number of transgenic N. benthamiana (35S::CsBRC) and WT. Bar = 5 cm. P values were determined using two‐tailed Student's t tests. Significant levels: ****P < .0001; ***P < .001. Data are presented as mean SD (n = 10).
Analysis of differential gene expression levels in Brassinolide and auxin synthesis and signaling pathways. (a) Brassinosteroid KEGG synthesis pathway. (b) Differential gene expression in brassinosteroids synthesis pathways of WT and transgenic tobacco. (c) Auxin KEGG synthesis pathway. (d) Differential gene expression in auxin synthesis pathways of WT and transgenic tobacco. (e) Differential gene expression of auxin transporters PIN in WT and transgenic tobacco. In (a) and (c), the up‐regulated genes are in the red box, and the purple box is the non‐differential gene.
Phenotype of transgenic rice and statistical analysis of transgenic rice yield. (a) Spike number per plant. Bar = 5 cm. (b) Panicle phenotype. Bar = 5 cm. (c) Comparison of tiller number. (d) Comparison of spike number per plant. (e) Main stem panicle comparison. Bar = 5 cm. (f) Grain width. Bar = 2 cm. (g) Grain length. Bar = 2 cm. (h) Comparison of spike length of main stem. (i) Comparison of grain number per spike of main stem. (g–m) Seed setting rate, 1,000‐grain weight, grain length comparison, and grain width comparison. P values were determined using two‐tailed Student's t tests. Significant levels: ****P < .0001; ***P < .001; **P < .01; *P < .05. Data are presented as mean SD (n = 10).
Overexpression of CsBRC, an F‐box gene from Camellia sinensis, increased the plant branching in tobacco and rice
  • Article
  • Full-text available

July 2024

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35 Reads

Bokun Zhou

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Qi Sheng

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Xinzhuan Yao

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Litang Lu

Tea plant (Camellia sinensis [L.]) is one of the most important crops in China, and tea branch is an important agronomic trait that determines the yield of tea plant. In previous work focused on GWAS that detecting GWAS signals related to plant architecture through whole genome re‐sequencing of ancient tea plants, a gene locus TEA 029928 significantly related to plant type was found. Sequence alignment results showed that this gene belonged to the F‐box family. We named it CsBRC. CsBRC‐GFP fusion proteins were mainly localized in the plasma membrane. By comparing the phenotypes of CsBRC transgenic tobacco and WT tobacco, it was found that the number of branches of transgenic tobacco was significantly higher than that of wild‐type tobacco. Through RNA‐seq analysis, it was found that CsBRC affects the branching development of plants by regulating the expression of genes related to brassinosteroid synthesis pathway in plants. In addition, overexpression of CsBRC in rice could increase tiller number, grain length and width, and 1,000‐grain weight.

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Figure 3. K-means clustering groups of the profile of expression of the differential metabolites of HT and IT. The x axis represents the different samples, while the y axis represents the standardized content per metabolite.
Figure 4. Differential abundance score map of the KEGG enrichment map of differential metabolites. (A) KEGG enrichment map of differential metabolites. The abscissa represent the corresponding rich factor of each pathway. The ordinate represents the pathway name, while the color of dot reflects the p-value. Dots that are redder indicate more significant enrichment. The size of the dots represents the number of enriched differential metabolites. (B) Differential abundance score map. (The horizontal axis represents the differential abundance (DA) score, while the vertical axis represents the differential pathway name. The overall amount of change in all the metabolites in the metabolic pathway is reflected by the DA score. A score of 1 indicates that the trend of expression of all the metabolites identified in this pathway is upregulated, while −1 indicates that the trend of expression of all the metabolites identified in this pathway is downregulated. The line segment describes two parameters for the pathway. Its length represents the absolute value of the DA score, while the size of dots at the endpoints represents the number of differential metabolites. The dots that are distributed on the left side of the central axis and have a longer line segment are more likely to indicate the downregulation of the overall expression of the pathway. The dots that are distributed on the right side of the central axis and have a longer line segment indicate that the overall expression of the pathway is more likely is to be upregulated. Larger dots indicate that the number of metabolites is greater. The color of the line segment and dot reflects the size of the p-value. Dots that are closer to red have a smaller p-value, while those that are closer to purple have a larger pvalue).
A list of 98 metabolites identified in HT and IT with potential roles in disease resistance.
Cont.
Identification of Nutritional Ingredients and Medicinal Components of Hawk Tea and Insect Tea Using Widely Targeted Secondary Metabolomics

April 2023

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64 Reads

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5 Citations

Horticulturae

In this study, the metabolites in insect tea and hawk tea were analyzed by ultra-high performance liquid chromatography–triple quadrupole mass spectrometry. We found 49 metabolites in insect tea and hawk tea that can be used as key active components in traditional Chinese medicine, as well as 98 metabolites that can be used as active components of pharmaceutical preparations for the treatment of cancers, hypertension, cardiovascular diseases, etc. Comparative analysis found that insect tea and hawk tea had significant differences in their metabolic profiles. Insect tea contains more metabolites beneficial to human health than hawk tea; insect tea also has higher antioxidant activity in vitro than hawk tea. The results of this study will contribute to the development of new health foods using insect tea.

Citations (1)


... Herein, astragalin, kaempferol-3-glucuronide, and tribuloside belonged to flavonoids. Sheng et al. applied widely targeted metabolomics to identify the nutritional components of hawk tea 20 . The results showed that metabolites such as adenosine, astragalin, tribuloside, (-)-epicatechin, kaempferol, etc. are also the main components of TCHT and IHT 20 . ...

Reference:

Metabolic profiles and potential antioxidant mechanisms of hawk tea
Identification of Nutritional Ingredients and Medicinal Components of Hawk Tea and Insect Tea Using Widely Targeted Secondary Metabolomics

Horticulturae