Fusarium wilt is an economically important disease of tomatoes, caused
by the soil-born fungus Fusarium oxysporum f. sp. lycopersici. There
are three host-specific races of this pathogen. The dominant tomato ge
ne I-2 confers resistance to race 2. The I-2 fusarium resistance gene
was mapped genetically to chromosome 11 of tomato; between the RFLP ma
rkers TG105 and TG36, 0.4 centiMorgan (cM) from TG105. A mean value of
43 kb for each cM was assigned in the vicinity of I-2. We have genera
ted new RFLP markers in the region by chromosome walking from TG105 to
wards 1-2 on lambda clones, and by subcloning a 350 kb long YAC clone
(YAC 8) that contains TG105. These RFLP markers were mapped physically
on YAC 8 by PFGE. The location of I-2 relative to these markers was g
enetically estimated using a recombinant inbred (RI) segregating popul
ation. The order of the markers according to the RI population is inco
nsistent with their order on the physical map. A cDNA clone, D14, that
was isolated by YAC 8, turned out to be 53% similar to xanthine dehyd
rogenase from mammals and flies. Antibodies raised against a part of t
he protein encoded by D14 recognize cross reacting material of MW 80 k
D, that is highly enriched in nodules of legumes, and seems to be indu
ced by various environmental and pathogenic stress conditions.