The use of resistant cultivars is the most effective method for contro
lling soybean cyst nematode (Heterodera glycines Ichinoe; SCN) on soyb
ean [Glycine max (L.) Merrill]. However, resistance to SCN is oligogen
ic, making inheritance patterns complex and breeding difficult. One ma
jor partial-resistance locus for SCN resistance is located on molecula
r Linkage group (MLG) 'G'. This locus controls more than 50% of variat
ion associated with response to SCN and resistant alleles are present
in many important sources of SCN resistance, including PI 209332, PI 8
8788, PI 90763, PI 437654, and 'Peking'. Restriction fragment length p
olymorphisms (RFLPs) Linked to the major SCN resistance alleles on MLG
G have proven effective in tracking the alleles and predicting SCN re
sponse. These RFLPs are much more efficient in terms of time and labor
than greenhouse assays for SCN. Nevertheless, more efficient DNA mark
ers are needed to screen the many lines required for marker-assisted s
election. Polymerase chain reaction-based markers, such as microsatell
ites (simple sequence repeats), have been sought because they are fast
er, less expensive, more polymorphic, and require less labor than RFLP
s. In this study, we report two microsatellites, BARC-Satt038 and BARC
-Satt130, that flank the major SCN resistance locus on MLG G. These mi
crosatellites efficiently identify the chromosome fragment carrying th
e resistance allele and are also good predictors of SCN phenotype resp
onse.