Ginkgo biloba seeds contain toxic ginkgotoxin (MPN) and its glucoside (MPNG), but their biosynthetic genes are poorly understood. To identify these genes, we performed multi-stage transcriptome sequencing, DEG screening, WGCNA, and enrichment analysis during seed development. MPNG accumulation predominated in mature seeds, correlating with gene expression dynamics. We identified 25 O-methyltransferase (OMT) and 40 UDP-glucosyltransferase (UGT) candidates. Among these, seven OMTs (e. g. , Gb₃5680, Gb₀1186) and eight UGTs (e. g. , Gb₃4745, Gb₃7494) were significantly upregulated during maturation, confirmed by qRT-PCR. WGCNA revealed four gene modules strongly correlated with MPN/MPNG accumulation, enriched in methylation, glycosylation, and secondary metabolite biosynthesis. This study integrates dynamic transcriptome and co-expression analyses to pinpoint key regulatory nodes in ginkgo toxin biosynthesis, providing novel genetic targets for developing low-toxicity cultivars through molecular breeding.
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Shi et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69df2ae6e4eeef8a2a6afe8e — DOI: https://doi.org/10.1093/pcp/pcag046
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Manman Shi
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Plant and Cell Physiology
Xidian University
Nanjing Forestry University
Suizhou Central Hospital
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