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Article

Comparative Metabolome and Transcriptome Analyses Reveal the Regulatory Mechanism of Purple Leafstalk Production in Taro (Colocasia esculenta L. Schott)

1
Guangdong Key Laboratory for New Technology Research of Vegetables, Vegetable Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510642, China
2
College of Horticulture, South China Agricultural University, Guangzhou 510642, China
3
Department of Horticulture, Faculty of Agriculture, Sher-e-Bangla Agricultural University, Dhaka 1207, Bangladesh
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Genes 2024, 15(1), 138; https://doi.org/10.3390/genes15010138
Submission received: 10 December 2023 / Revised: 15 January 2024 / Accepted: 18 January 2024 / Published: 22 January 2024
(This article belongs to the Section Plant Genetics and Genomics)

Abstract

Taro is a plant in the Araceae family, and its leafstalk possesses significant botanical and culinary value owing to its noteworthy medicinal and nutritional attributes. Leafstalk colour is an essential attribute that significantly influences its desirability and appeal to both breeders and consumers. However, limited information is available about the underlying mechanism responsible for the taro plant’s colouration. Thus, the purpose of the current study was to elucidate the information on purple leafstalks in taro through comprehensive metabolome and transcriptome analysis. In total, 187 flavonoids, including 10 anthocyanins, were identified. Among the various compounds analysed, it was observed that the concentrations of five anthocyanins (keracyanin chloride (cyanidin 3-O-rutinoside chloride), cyanidin 3-O-glucoside, tulipanin (delphinidin 3-rutinoside chloride), idaein chloride (cyanidin 3-O-galactoside), and cyanidin chloride) were found to be higher in purple taro leafstalk compared to green taro leafstalk. Furthermore, a total of 3330 differentially expressed genes (DEGs) were identified by transcriptome analysis. Subsequently, the correlation network analysis was performed to investigate the relationship between the expression levels of these differentially expressed genes and the content of anthocyanin. There were 18 DEGs encoding nine enzymes detected as the fundamental structural genes contributing to anthocyanin biosynthesis, along with seven transcription factors (3 MYB and 4 bHLH) that may be promising candidate modulators of the anthocyanin biosynthesis process in purple taro leafstalk. The findings of the current investigation not only provide a comprehensive transcriptional code, but also give information on anthocyanin metabolites as well as beneficial insights into the colour mechanism of purple taro leafstalk.
Keywords: taro leafstalk; metabolome; transcriptome; anthocyanins taro leafstalk; metabolome; transcriptome; anthocyanins

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MDPI and ACS Style

Jiang, S.; Guo, J.; Khan, I.; Jahan, M.S.; Tang, K.; Li, G.; Yang, X.; Fu, M. Comparative Metabolome and Transcriptome Analyses Reveal the Regulatory Mechanism of Purple Leafstalk Production in Taro (Colocasia esculenta L. Schott). Genes 2024, 15, 138. https://doi.org/10.3390/genes15010138

AMA Style

Jiang S, Guo J, Khan I, Jahan MS, Tang K, Li G, Yang X, Fu M. Comparative Metabolome and Transcriptome Analyses Reveal the Regulatory Mechanism of Purple Leafstalk Production in Taro (Colocasia esculenta L. Schott). Genes. 2024; 15(1):138. https://doi.org/10.3390/genes15010138

Chicago/Turabian Style

Jiang, Shizheng, Juxian Guo, Imran Khan, Mohammad Shah Jahan, Kang Tang, Guihua Li, Xian Yang, and Mei Fu. 2024. "Comparative Metabolome and Transcriptome Analyses Reveal the Regulatory Mechanism of Purple Leafstalk Production in Taro (Colocasia esculenta L. Schott)" Genes 15, no. 1: 138. https://doi.org/10.3390/genes15010138

APA Style

Jiang, S., Guo, J., Khan, I., Jahan, M. S., Tang, K., Li, G., Yang, X., & Fu, M. (2024). Comparative Metabolome and Transcriptome Analyses Reveal the Regulatory Mechanism of Purple Leafstalk Production in Taro (Colocasia esculenta L. Schott). Genes, 15(1), 138. https://doi.org/10.3390/genes15010138

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