The upper bands were comparatively larger than expected and were revealed to be artifacts in PCR amplification (Band-C and Band-D in Fig. 1). Multiple band artifacts are common in the amplification of SSR sequences and can generally be removed by modifying the PCR conditions or the number of cycles [22], [23] and [24]. Selleck Perifosine However, the examples described here are fundamentally different from the previous reports for two reasons: firstly, the larger bands could not be abolished by altering the PCR conditions; and, secondly, the reamplification of the larger bands showed the same band patterns as that of preliminary

PCR amplification. Based on all these findings together, it appears that the artifact bands are derived from heteroduplexes created by the combining and interruption between coexisting different amplicons. The appearance of multiple bands in PCR products has been regarded as one of the more serious obstacles to marker development and genetic mapping for recently duplicated plant genomes such as rapeseed (Brassica napus) [25] and P. ginseng [9] because they hinder genotyping against the mapping population as well as the authentication of cultivars. In

this study, a clear single band was successfully amplified by using a locus-specific primer designed on the basis of sequence variation between the two paralogous loci. The locus-specific primer was based on the SNP sequence of the polymorphic band of the gm47n marker. In addition to the SNP, T/C in CH5424802 purchase Band-B and Band-A, we added another modified nucleotide, “G” instead of “A”, that resulted in a clear single band of PCR product in ginseng, as suggested by a previous report [17]. The clear single band was polymorphic between two cultivars, Chunpoong and Yunpoong, and segregated with a Mendelian single gene pattern in their F2 population ( Fig. 4). These results support our assumption that Band-A and Band-B are not heterozygous

forms, but instead are derived from different loci created by the recent genome duplication of P. ginseng [7]. Our method can be applied to other markers to overcome the genotyping difficulty caused by multiple bands in P. ginseng. Most plant species have undergone a few rounds of genome duplication [26] and [27]. We suggest Gefitinib concentration that this approach should be considered as an efficient method to avoid the misinterpretation of multiple band appearances in genome research on wild plant resources that may have undergone recent genome duplication. Utilization of upcoming ginseng genome sequence information will be a powerful tool for the development of indisputable and reliable markers and genetic mapping in P. ginseng. We are conducting whole-genome sequencing for the cultivar Chunpoong using the Illumina platform [28] and have identified many long paralogous genome sequence pairs from the draft sequence assembly. Each of the paralogous sequences can be mapped by developing paralogous locus-specific markers as suggested in this study.