From fruiting bodies of L. edodes strain L-54, single-spore isolates (SSIs) were collected. Two parental types of L-54 were regenerated via monokaryotization. By means of random-amplified polymorphic DNA (RAPD), DNA samples from L-54, its two parental types, and 32 SSIs were amplified with arbitrary primers. Dedikaryotization was demonstrated, and 91 RAPD-based molecular markers were generated. RAPD markers that were segregated at a 1:1 ratio were used to construct a linkage map of L. edodes. This RAPD-linkage map greatly enhanced the mapping of other inheritable and stable markers [such as those that are linked to a phenotype (the mating type), a known gene (priA) and a sequenced DNA fragment (MAT)] with the aid of mating tests, bulked-segregant analysis, and PCR-single-strand conformational polymorphism. These markers comprised a genetic map of L. edodes with 14 linkage groups and a total length of 622.4 cM. © BSRK & Springer-Verlag 2002.
CITATION STYLE
Hoi-Shan, K., & Hai-Lou, X. (2002). Construction of a genetic linkage map of shiitake mushroom Lentinula Edodes strain L-54. Journal of Biochemistry and Molecular Biology, 35(5), 465–471. https://doi.org/10.5483/bmbrep.2002.35.5.465
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