Identification of genetic variants controlling diosgenin content in Dioscorea zingiberensis tuber by genome-wide association study

被引:0
|
作者
Sun, Shi Xian [1 ]
Li, Yanmei [2 ]
Jia, Lu [2 ]
Ye, Shili [3 ]
Luan, Yunpeng [4 ,5 ]
机构
[1] Southwest Forestry Univ, Yunnan Key Lab Plateau Wetland Conservat Restorat, Kunming 650224, Peoples R China
[2] Southwest Forestry Univ, Sch Life Sci, Dept Life Technol Teaching & Res, Kunming 650224, Peoples R China
[3] Southwest Forestry Univ, Fac Math & Phys, Kunming 650224, Peoples R China
[4] Yunnan Univ Tradit Chinese Med, Affiliated Hosp 1, Kunming 650021, Peoples R China
[5] Southwest Forestry Univ, Key Lab Forest Resources Conservat & Utilizat Sout, Minist Educ, Kunming 650224, Peoples R China
来源
BMC PLANT BIOLOGY | 2024年 / 24卷 / 01期
关键词
Dioscorea Zingiberensis; Diosgenin; Breeding; P450; Enzyme; STEROIDAL SAPONINS; SOFTWARE; COMPLEX; CULTURE; CLONING; TRAITS; WRIGHT;
D O I
10.1186/s12870-024-05133-1
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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.
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页数:11
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