An F-2 population developed from the Xa-4 near isogenic lines, IR24 and IRB
B4, was used for fine mapping of the rice bacterial blight resistance gene,
Xa-4. Some restriction fragment length polymorphism (RFLP) markers on the
high-density map constructed by Harushima et at. and the amplified DNA frag
ments homologous to the conserved domains of plant disease resistance (R) g
enes were used to construct the genetic linkage map around the gene Xa-4 by
scoring susceptible individuals in the population. Xa-4 was mapped between
the RFLP marker G181 and the polymerase chain reaction (PCR) marker M55. T
he R gene homologous fragment marker RS13 was found co-segregating with Xa-
4 by analyzing all the plants in the population. This result opened an appr
oach to map-based cloning of this gene, and marker RS13 can be applied to m
olecular marker-assisted selection of Xa-4 in rice breeding programs.