Abstract
A genomic library enriched with (gT)n repeats from tartary buckwheat (Fagopyrum tataricum) was constructed using 5′-anchored PCR for the development of microsattellite markers. Sequencing analysis of 5 clones from the library showed that they all contained microsatellites (totally 10 loci), and each was unique. An additional locus-specific primer was designed according to flanking sequence. Two of the microsatellite loci of 10 tartary buckwheat varieties were amplified using an anchored primer and a locus-specific primer, which revealed a clear polymorphic pattern. The data confirmed that the degenerate primer was reliably anchoring at the 5′-end of the microsatellite, and the primers developed based on this technology could be used for diversity analysis of tartary buckwheat.
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Acknowledgments
This work was supported by The program of International Plant Genetic Resources Institute (LOAAPO04074) and programs of Science and Technology of Shanxi province, China(041147, 2006031047).
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Li, YQ., Shi, TL. & Zhang, ZW. Development of microsatellite markers from tartary buckwheat. Biotechnol Lett 29, 823–827 (2007). https://doi.org/10.1007/s10529-006-9293-2
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DOI: https://doi.org/10.1007/s10529-006-9293-2