Perilla () is an economically and culturally important plant in East Asia. Plant breeding between cultivars has enhanced the genetic diversity of perilla overall, but means that functionally diverse subspecies are more difficult to identify and distinguish. In this study, we developed gene-based DNA markers to distinguish between the Korean herbal medicinal perilla varieties. We identified informative simple sequence repeat (SSR) regions on the promoter regions of the - and dihydroflavonol 4-reductase () genes, as well as a large insertion-deletion (indel) region in the limonene synthase () gene, and developed markers to characterize the distinct subspecies differences (-, , and , respectively). Using the primers, a 430-bp region could be amplified from . var. , , and f. (known as Jasoyeop, Jureum-soyeop, and Chungsoyeop, respectively), but not from . var. (Dlggae). The primers resulted in PCR products of 314 or 316, 330, 322, and 315 bp from Dlggae, Jasoyeop, Jureum-soyeop, and Chungsoyeop, respectively, and the primers resulted in products of 189 or 202, 187 or 189, 185 or 189, and 193bp, respectively, for the four perilla subspecies. Combining these three reactions into a single multiplex PCR approach resulted in subspecies-specific PCR band patterns for six common types of commercial perilla, distinguishing between three varieties of Dlggae (Cham-Dlggae, Ip-Dlggae, and Bora-Dlggae), as well as identifying Jasoyeop, Jureum-soyeop, and Chungsoyeop. These user-friendly markers will be valuable as a simple and efficient method for identifying the Korean medicinal herb Jasoyeop, as well as distinguishing between other functionally distinct subspecies, which may have broad applications in the Korean herbal industry.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154563PMC
http://dx.doi.org/10.3390/molecules22040665DOI Listing

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