4.6 Article

Diosgenin biosynthesis investigation in medicinal herb (Tribulus terrestris) by transcriptome analysis

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GENE
卷 893, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.gene.2023.147937

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Tribulus terrestris; Transcriptome analysis; Diosgenin biosynthesis; Transcription factor; Homology; SSRs

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This study aimed to identify candidate genes associated with diosgenin biosynthesis in Tribulus terrestris through whole transcriptome profiling. The majority of unigenes related to the biosynthesis of diosgenin exhibited up-regulation in the fruit, leaf, and root tissues. The differential expression of selected genes was validated through qRT-PCR. Additionally, the study discovered a large number of unigenes related to transcription factors and containing simple sequence repeats (SSR).
Next-generation sequencing (NGS) has revolutionized the analysis of specific genes, pathways, and their regulation in various species. Tribulus terrestris L., an annual medicinal herb of Zygophyllaceae family, has gained significant attention due to its diverse medicinal properties, including anti-inflammatory, antimicrobial, and anti-cancer effects. Diosgenin, a steroidal saponin, is the major bioactive compound responsible for the medicinal importance of T. terrestris. However, there is a paucity of information regarding the genes involved in the diosgenin biosynthetic pathway in T. terrestris. To address this gap, this study aimed to identify candidate genes associated with diosgenin biosynthesis through whole transcriptome profiling. A total of similar to 7.9 GB of data, comprising 482 million reads, was obtained and assembled into 148,871 unigenes. Subsequently, functional annotations were assigned to 50 % of the unigenes using sequence similarity searches against the NCBI non-redundant (NR), Uniprot, KEGG, Pfam, GO, and COG databases, primarily based on Gene Ontology and KEGG-KAAS pathways. The majority of unigenes associated with the biosynthesis of the steroidal diosgenin backbone exhibited up-regulation in the fruit, leaf, and root tissues, except the SQE gene in root. The differential expression of selected genes was further validated through quantitative real-time polymerase chain reaction (qRT-PCR). Additionally, the study identified 21,026 unigenes related to transcription factors and 15,551 unigenes containing simple sequence repeats (SSR). Notably, di-nucleotide SSR motifs exhibited a high repeat frequency. These findings greatly enhance our understanding of the diosgenin biosynthesis pathway and provide a basis for future research in molecular investigation and metabolic engineering, specifically for boosting diosgenin content.

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