Amplified fragment length polymorphism (AFLP) and microsatellite (simple se
quence repeat, SSR) techniques were used to map the Rcs(Peking) gene, which
is resistant to most isolates of Cercospora sojina in the soya bran cultiv
ar 'Peking'. The mapping was conducted using a defined F-2 population deriv
ed from the cross of 'Peking' (resistant) x 'Lee' (susceptible). Of 64 EcoR
I and MseI primer combinations, 30 produced polymorphisms between the two p
arents. The F-2 population, consisting of 116 individuals, was screened wit
h the 30 AFLP primer pairs and three mapped SSR markers to detect markers p
ossibly linked to Rcs(Peking). One AFLP marker amplified by primer pair E-A
AC/M-CTA and one SSR marker Satt244 were identified to be linked to Rcs(Pek
ing). The gene was located within a 2.1-cM interval between markers AACCTA1
78 and Satt244, 1.1 cM from Satt244 and 1.0 cM from AACCTA178. Since the SS
R markers Satt244 and Satt431 have been mapped to molecular linkage group (
LC) J of soya bean, the Rcs(Peking) resistance gene was putatively located
on the LG J. This will provide soya bean breeders an opportunity to use the
se markers For marker-assisted selection for frogeye leaf spot resistance i
n soya bean.