Genetic and linkage analysis of marker loci were performed with 4 self
ed progenies, derived from single plant (I-0/1 lines) of carrot (Daucu
s carota L. sativus). The analysis of 58 markers included 1 morphologi
cal marker, 10 isozyme loci, 14 RFLPs, 28 RAPD markers, and 6 isolated
PCR fragments used as RFLP probes. Linkage analysis was carried out w
ith the MAPMAKER program and resulted in the construction of 8 linkage
groups containing 55 markers with an average distance of 13.1 cM, 3 m
arker loci remained unlinked. 24% of the markers deviated significantl
y from the expected Mendelian ratios (1:2:1 or 3:1)due to gametic or z
ygotic selection. It was shown that isolated PCR amplification product
s can be used as RFLP probes to detect polymorphisms for a certain loc
us in progenies where the corresponding RAPD pattern is monomorphic or
no amplification product is observed. Since carrot has a relative sma
ll genome the probability of amplifying repetitive DNA sequences is co
mparatively low. Thus PCR amplification products represent an addition
al useful source of RFLP probes.