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Miscanthus sinensis has high biomass yield and contributed two of the three genomes in M.x giganteus,a bioenergy crop widely studied in Europe and North America,and thus is a potential biomass crop and an important germplasm for Miscanthus breeding.Molecular markers are essential for germplasm evaluation,genetic analyses and new cultivar development in M.sinensis.In the present study,we reported transferability of simple sequence repeat (SSR) markers from Brachypodium distachyon to M.sinensis.A set of 57 SSR markers evenly distributed across the B.distachyon genome were deliberately designed.Out of these B.distachyon SSR markers,86.0% are transferable to M.sinensis.The SSR loci amplified in M.sinensis were validated by re-sequencing the amplicons.The polymorphism information content (PIC) of the transferable SSR markers varied from 0.073 to 0.375 with a mean of 0.263,assessed based on 21 M.sinensis genotypes.Phylogenetic tree based on 162 alleles detected by 49 SSR markers could unambiguously distinguish B.distachyon from M.sinensis,and cluster 21 M.sinensis genotypes into three groups that are basically in coincidence with their geographical distribution and ecotype classifications.The markers developed by the comparative genomic approach could be useful for germplasm evaluation,genetic analysis,and marker-assisted breeding in Miscanthus.
Miscanthus sinensis has high biomass yield and contributed two of the three genomes in Mx giganteus, a bioenergy crop widely studied in Europe and North America, and thus is a potential biomass crop and an important germplasm for Miscanthus breeding. Molecular markers are essential for germplasm evaluation , genetic analyzes and new cultivar development in M.sinensis. the present study, we reported transferability of simple sequence repeat (SSR) markers from Brachypodium distachyon to M.sinensis. A set of 57 SSR markers evenly distributed across the B.distachyon genome were deliberately designed. Of these B. difficile SSR markers, 86.0% are transferable to M. sinensis. The SSR loci amplified in M. sinensis were validated by re-sequencing the amplicons. Polymorphism information content (PIC) of the transferable SSR markers varied from 0.073 to 0.375 with a mean of 0.263, assessed based on 21 M. sinensis genotypes. Phylogenetic tree based on 162 alleles detected by 49 SSR markers could unambi guously distinguish B.distachyon from M.sinensis, and cluster 21 M.sinensis genotypes into three groups that are basically in coincidence with their geographical distribution and ecotype classifications. The markers developed by the comparative genomic approach could be useful for germplasm evaluation, genetic analysis , and marker-assisted breeding in Miscanthus.