A Brassica oleracea linkage map was constructed from an F, population
of 69 individuals with sequences previously mapped independently in th
ree linkage maps of this species. These were the maps published by Kia
nian and Quires (1992), Landry et al. (1992), and Camargo et al. (1997
). The base map developed in this study consisted of 167 RFLP loci in
nine linkage groups, plus eight markers in four linkage pairs, coverin
g 1738 cM. Linkage group alignment was also possible with a fourth map
published by Ramsay ct al. (1996), that contained loci in common with
the map of Camargo et al. (1997). Common sequences across the mapping
populations served to align most of the linkage groups of the indepen
dently developed maps. In general, consistent linear order among marke
rs was maintained, although often the distances between markers varied
from map to map. A linkage group in the map of Landry ct al. carrying
a clubroot resistance QTL and consisting of markers from two other li
nkage groups, was found to be rearranged. This was not surprising, con
sidering that the resistance gene was introgressed from Brassica napus
. The extensively duplicated nature of the C genome was revealed by 19
sequences detecting duplicated loci within chromosomes and 17 sequenc
es detecting duplicated loci between chromosomes. The variation in map
ping distances between linked loci pairs on different chromosomes demo
nstrated that sequence rearrangement is a distinct feature of this gen
ome. Although the consolidation of all linkage groups in the four B. o
leracea maps compared was not possible, the present work served to add
a considerable number of markers to corresponding linkage groups. Som
e of the chromosome segments in particular, were enriched with many ma
rkers that may be useful for future gene tagging or cloning. It will b
e possible in the future to complete the consolidation of all four map
s as new loci are added to each map.