Genetically modified (GM) crops have been developed to enhance various agronomic traits and increase the production of functional compounds. In the present study, the major agronomic characteristics of protopanaxadiol (PPD)-enriched GM rice, which was developed by introducing dammarenediol-II synthase (PgDDS) and protopanaxadiol synthase (CYP716A47) genes from Panax ginseng into Oryza sativa cv. Dongjin, were evaluated. The stability of the introduced genes was confirmed using PCR and immunostrip tests, which showed consistent expression across multiple generations (T5-T7). Agronomic traits, including days to heading, culm length, panicle length, tiller number, and grain weight per plant, were compared between GM rice and its non-GM counterpart, Dongjin rice. No significant differences were observed for these traits, indicating that genetic modification did not affect the overall plant growth. However, seed morphology analyses revealed that PPD-enriched GM rice had significantly longer brown rice grains. In contrast, other seed traits remained within the natural range of commercial rice varieties. Furthermore, PPD was consistently detected in GM rice, whereas it was absent in non-GM Dongjin rice. These findings suggest that PPD-enriched GM rice maintains a stable agronomic performance while successfully accumulating PPD, supporting its potential as a functional crop. However, further research is required to evaluate its environmental impact, food safety, and efficacy as a functional food source.

A dwarf mutant rice line was selected from an Ac/Ds insertion mutant population and named dwf1. The phenotype of F₁ and F₂ plants derived from a cross between dwf1 and Dongjin indicated that a single recessive gene is responsible for the mutant phenotype, and we named this gene dwf1. Resequencing of the dwf1 line and Dongjin (wild type) revealed 42,386 homozygous single nucleotide polymorphisms (SNPs) between dwf1 line and Dongjin. MutMap analysis was performed by sequencing a DNA pool prepared from 100 mutant type plants in the dwf1/Dongjin F₂ population, and it was found that the dwf1 gene was located in the 23 ~ 30 Mbp region on chromosome 4. In this region, we found a non-synonymous SNP in the Os04g0469800 gene, which was reported as D11 gene encoding a cytochrome P450 family protein involved in the biosynthesis of brassinosteroids (BRs). This SNP was regarded as the causative SNP for the dwf1 phenotype, and the dwf1 gene is a novel allele of D11. We performed mapping of the dwf1 gene with five SNP markers on chromosome 4 with 190 dwf1/Dongjin F₂ plants. The phenotype of F₂ plants was completely co-segregated with genotypes of the J10402 marker, which was developed based on the non-synonymous SNP in the D11 gene. These results will contribute to the study of the molecular biological functions of the D11 gene and BRs.