The genetic variability in the Brassica juncea cultivars was detected
by employing in-gel hybridization of restricted DNA to simple repetiti
ve sequences such as (GATA)(4), (GACA)(4) and (CAC)(5). The most infor
mative probe/enzyme combination was (GATA)(4)/EcoRI, yielding highly p
olymorphic fingerprint patterns for the B. juncea cultivars. This tech
nique was found to be dependable for establishing the variety specific
patterns for most of the cultivars studied, a prerequisite for germpl
asm preservation. The results of the present study were compared with
those reported in our earlier study in which random amplification of p
olymorphic DNA (RAPD) was used for assessing the genetic variability i
n the B. juncea cultivars.