Author:
Sun Shi xian,Li Yanmei,Jia Lu,Ye Shili,Luan Yunpeng
Abstract
Abstract
Background
Diosgenin is an important steroidal precursor renowned for its diverse medicinal uses. It is predominantly sourced from Dioscorea species, particularly Dioscorea zingiberensis. Dioscorea zingiberensis has an ability to accumulate 2–16% diosgenin in its rhizomes. In this study, a diverse population of 180 D. zingiberensis accessions was used to evaluate the genomic regions associated with diosgenin biosynthesis by the genome wide association study approach (GWAS).
Results
The whole population was characterized for diosgenin contents from tubers by gas chromatography mass spectrometry. The individuals were genotyped by the genotyping-by-sequencing approach and 10,000 high-quality SNP markers were extracted for the GWAS. The highest significant marker-trait-association was observed as an SNP transversion (G to T) on chromosome 10, with 64% phenotypic variance explained. The SNP was located in the promoter region of CYP94D144 which is a member of P450 gene family involved in the independent biosynthesis of diosgenin from cholesterol. The transcription factor (TF) binding site enrichment analysis of the promoter region of CYP94D144 revealed NAC TF as a potential regulator. The results were further validated through expression profiling by qRT-PCR, and the comparison of high and low diosgenin producing hybrids obtained from a bi-parental population.
Conclusions
This study not only enhanced the understanding of the genetic basis of diosgenin biosynthesis but also serves as a valuable reference for future genomic investigations on CYP94D144, with the aim of augmenting diosgenin production in yam tubers.
Funder
Reserve Talents Project for Young and Middle-aged Academic and Technical Leaders of Yunnan Provincial Department of Science and Technology
Publisher
Springer Science and Business Media LLC
Reference53 articles.
1. Sonawane PD, Pollier J, Panda S, Szymanski J. Plant cholesterol biosynthetic pathway overlaps with phytosterol metabolism. Nat Plants. 2016;3(1):16205. https://doi.org/10.1038/nplants.2016.205.
2. Chaturvedi HC, Kidwai MJNR. Cloning of medicinal plants through tissue culture–a review. Indian J Exp Biol. 2007;45(11):937–48.
3. Wang Y, Zhang Y, Zhu Z, Zhu S. Exploration of the correlation between the structure, hemolytic activity, and cytotoxicity of steroid saponins. Bioorg Med Chem. 2007;15(7):2528–32.
4. Bertrand J, Liagre B, Bégaud-Grimaud G, Jauberteau MO. Analysis of relationship between cell cycle stage and apoptosis induction in K562 cells by sedimentation field-flow fractionation. J Chromatogr B. 2009;877(11):1155–61.
5. Zhang R, Li P, Xu L, Chen Y. Enhancement of diosgenin production in Dioscorea zingiberensis cell culture by oligosaccharide elicitor from its endophytic fungus fusarium oxysporum Dzf17. Nat Prod Commun. 2009;4(11):1459–62.