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The Journal of Heredity 1996:87(3):214-218
© 1996 The American Genetic Association 87:214-218

research-article

A Linkage Map of Sweet Cherry Based on RAPD Analysis of a Microspore-Derived Callus Culture Population

E. J. Stockinger, C. A. Mulinix, C. M. Long, T. S. Brettin, and A. F. lezzoni

From the Departments of Crop and Soil Sciences (Stockinger) and Horticulture (Mulinix, Long, Brettin, and lezzonl), Michigan State University East Lansing, MI 48824

Contributing Editor. Scott V. Tingey

Abstract

A partial linkage map was constructed for the sweet cherry (Prunus avium L.) cultivar Emperor Francis from a population of 56 microspore-derived callus culture Individuals. The callus cultures were genotyped for two allozymes and 90 random amplified polymorphic DNA (RAPD) markers using 79 random decanucleotide DNA primers and the polymerase chain reaction (PCR). Eighty-nine markers mapped to 10 linkage groups totaling 503.3 cM. DNA blot and hybridization analysis using five cloned RAPDs as probes demonstrated that one of the decanucleotide primers amplified a region of the Emperor Francis genome containing a unique sequence, whereas the other four decanucleotide primers amplified regions of the Emperor Francis genome containing repeated sequences. The five cloned RAPD probes also recognized putative homologous regions in ground cherry, P. fruticosa Pall., and sour cherry, P. cerasus L., a naturally occurring allopolyploid between P. fruticosa and P. avium.


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