The genomic DNA clone RG28, linked to the major fragrance gene of rice (fgr
), was assessed for polymorphism in order to produce a PCR-based marker for
fragrance. A small mono-nucleotide repeat, that was polymorphic between a
pair of fragrant and non-fragrant cultivars, was identified and developed i
nto a co-dominant PCR-based marker. The polymorphism-information-content de
terminations for three microsatellite markers, that have been genetically m
apped near RG28, are also presented. These PCR-based markers will be highly
useful in distinguishing fragrance-producing alleles from non-fragrance-pr
oducing alleles at the fgr locus.