Yuting Jiao’s research while affiliated with South China Agricultural University and other places

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Publications (3)


Female mating behavior and attraction to sex pheromone peak in the evening. a Number of mated females at different time periods in a day (replicates = 5, F(2,12) = 690.6, P < 0.0001, one-way ANOVA). b Number of females attracted by sex pheromone at different time periods in a day (replicates = 8, F(2,21) = 54.83, P < 0.0001, one-way ANOVA). c Female EAG response to TMP at 8:00 and 20:00 (replicates = 5, P = 0.0295, independent sample t test). d Female EAG response to TTMP at 8:00 and 20:00 (replicates = 5, P = 0.0259, independent sample t test). e Female EAG response to TMP and TTMP mixture at 8:00 and 20:00 (replicates = 11, P = 0.0004, independent sample t test). f Example traces of female antenna responses to TMP. g Example traces of female antenna responses to TTMP. h Example traces of female antenna responses to mixture of TMP and TTMP
Tim and Pbp5 screened by transcriptome analysis may be associated with peaking mating behavior of females at 20:00 in a day. a The number of DEGs in the female head at 20:00 compared with those at other times. Up: significantly up expressed genes in the head of females at 20:00; down: significantly down expressed genes in the head of females at 20:00. b KEGG pathways enriched with the DEGs between female heads at 20:00 and 8:00. c Expression patterns of DEGs (between 20:00 and 8:00) in the circadian rhythm pathway at different times in a day. Before heat mapping, the FPKM values of the DEGs were processed using Z-score standardization. (d) Expression patterns of the olfactory genes in the head of females at different times in a day. Before heat mapping, the FPKM values were processed using Z-score standardization. e Relative expression verification of Tim in the head of females at different times in a day (replicates = 5, F(5,24) = 3.906, P = 0.0099, one-way ANOVA). f Relative expression verification of Pbp5 in the head of females at different times in a day (replicates = 5, F(2,24) = 5.866, P = 0.0011, one-way ANOVA)
Binding ability of Pbp5 to TMP and TTMP. a Binding sites prediction between Pbp5 and 1-NPN by Autodock Vina. b Binding sites prediction between Pbp5 and TMP by Autodock Vina. c Binding sites prediction between Pbp5 and TTMP by Autodock Vina. d Binding abilities of 1-NPN to Pbp5. e Competitive binding ability of TMP to 1-NPN and Pbp5 complex. f Competitive binding ability of TTMP to 1-NPN and Pbp5 complex. g Binding abilities of 1-NPN to Pbp5 mutant. h Competitive binding ability of TMP to 1-NPN and Pbp5 mutant complex. i Competitive binding ability of TTMP to 1-NPN and Pbp5 mutant complex
RNAi of Pbp5 reduces female mating and EAG response to TMP and TTMP. a Maximum likelihood topology tree shows Pbp5 is conserved in Tephritidae. b Conservation of Pbp5 amino acids in Tephritidae. The image was generated using the complete amino acid sequences of the species in Tephritidae in a. c Female tissue expression of Pbp5 (replicates = 5, F(3,16) = 82.79, P < 0.0001, one-way ANOVA). d Female tissue expression of Obp99a (replicates = 5, F(3,16) = 263.5, P < 0.0001, one-way ANOVA). e Influence of Obp99a knockdown on female mating (replicates = 6, P = 0.2722, paired sample t test). f Influence of Pbp5 knockdown on female mating (replicates = 6, P = 0.0047, paired sample t test). g Influence of Pbp5 knockdown on female EAG response to TMP (replicates = 19, P < 0.0001, independent sample t test). h Influence of Pbp5 knockdown on female EAG response to TTMP (replicates = 19, P = 0.0015, independent sample t test). i Influence of Pbp5 knockdown on female EAG response to TMP and TTMP mixture (replicates = 19, P = 0.0002, independent sample t test)
Influence of Tim on Pbp5 expression and female mating. a Tissue expression pattern of Tim in females (replicates = 5, F(3,16) = 70.45, P < 0.0001, one-way ANOVA). b RNAi efficiency of Tim (replicates = 5, P = 0.0001, independent sample t test). c Relative expression of Pbp5 in female antenna after Tim knockdown (replicates = 5, P < 0.0001, independent sample t test). d Influence of Tim knockdown on mated female number (replicates = 5, P = 0.0004, paired sample t test). e Expression patterns of Tim and Pbp5 in the head and antenna of females with biological clock reversed (Tim: replicates = 4, F(5,18) = 5.199, P = 0.004, one-way ANOVA; Pbp5: replicates = 4, F(5,18) = 4.954, P = 0.005, one-way ANOVA). f Mated number of females with biological clock reversed in the evening (replicates = 5, P < 0.0001, paired sample t test). g Mated number of females with biological clock reversed in the morning (replicates = 5, P < 0.0001, paired sample t test)
Expression of a pheromone binding protein affected by timeless gene governs female mating behavior in Bactrocera dorsalis
  • Article
  • Full-text available

February 2025

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123 Reads

Yuting Jiao

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Guohong Luo

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Background The rhythmic mating behavior of insects has been extensively documented, yet the regulation of this behavior through sex pheromone sensing olfactory genes affected by the clock genes in the rhythm pathway remains unclear. Results In this study, we investigated the impact of circadian rhythm on female recognition of male rectal Bacillus-produced sex pheromone in B. dorsolis. Behavioral and electrophysiological assays revealed a peak in both mating behavior and response to sex pheromones in the evening in females. Comparative transcriptome analysis of female heads demonstrated rhythmic expression of the Timeless gene-Tim and odorant binding protein gene-Pbp5, with the highest expression levels occurring in the evening. Protein structural modeling, tissue expression patterns, RNAi treatment, and physiological/behavioral studies supported Pbp5 as a sex pheromone binding protein whose expression is affected by Tim. Furthermore, manipulation of the female circadian rhythm resulted in increased morning mating activity, accompanied by consistent peak expression of Tim and Pbp5 during this time period. These findings provide evidence that insect mating behavior can be modulated by clock genes through their effects on sex pheromone sensing processes. Conclusions Our results also contribute to a better understanding of the molecular mechanisms underlying rhythmic insect mating behavior.

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Figure 3
A timeless gene-regulated pheromone binding protein governs female mating behavior in Bactrocera dorsalis

September 2024

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174 Reads

The rhythmic mating behavior of insects has been extensively documented, yet the regulation of this behavior through sex pheromone sensing olfactory genes controlled by the clock genes in the rhythm pathway remains unclear. In this study, we investigated the impact of circadian rhythm on female recognition of male rectal Bacillus-produced sex pheromone in B. dorsolis. Behavioral and electrophysiological assays revealed a peak in both mating behavior and response to sex pheromones in the evening in females. Comparative transcriptome analysis of female heads demonstrated rhythmic expression of the Timeless gene-Tim and odorant binding protein gene-Pbp5, with highest expression levels occurring in the evening. Protein structural modeling, tissue expression patterns, RNAi treatment, and physiological/behavioral studies supported Pbp5 as a sex pheromone binding protein whose expression is regulated by Tim. Furthermore, manipulation of female circadian rhythm resulted in increased morning mating activity, accompanied by consistent peak expression of Tim and Pbp5 during this time period. These findings provide evidence that insect mating behavior can be modulated by clock genes through their effects on sex pheromone sensing processes. Our results also contribute to a better understanding of the molecular mechanisms underlying rhythmic insect mating behavior.


Figure 1
Lysozyme Treatment Makes 16S rRNA Amplicon Sequencing Results Less Biased

November 2021

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168 Reads

Yuting Jiao

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Zijie Gao

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Shiyu Gui

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[...]

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Background Amplicon sequencing is widely applied in gut bacteria structure analysis. However, the proportion of Gram-positive bacteria may greatly affect the results of microbial community analysis. Lysozyme is an effective agent to extract DNA of Gram-positive bacteria. In this study, we assessed the influence of lysozyme treatment on results of Bactrocere dorsalis rectal bacteria structure. Result The results indicated that the total bacteria content can be significantly increased in lysozyme treated samples. Moreover, rectal bacteria diversity was significantly higher in lysozyme treated samples. A detail analysis revealed that abundance of Gram-positive bacteria significantly increased in samples treated with lysozyme. Conclusion This study indicates that lysozyme treatment before DNA extraction is an effective way to reduce bias in bacteria structure analysis, especially for samples with high proportion of Gram-positive bacteria.