Rust diseases are the major cause of low yield of wheat in
Pakistan. Wheat breeders all over the world as well as in
Pakistan are deriving rust resistance genes from alien
species like Triticum ventricosum and introducing
them in common wheat (Triticum aestivum). One such
example is the introgression of rust resistance gene cluster
Lr37-Sr38-Yr17 derived from T. ventricosum
chromosome 2NS into the common wheat. A basic prerequisite
to introduce alien rust resistance gene (like those present
on 2NS segment) in locally adapted varieties is availability
of a suitable marker system which can be used to keep track
of presence of newly added gene in the old background. In
this present study, one hundred and fifty Randomly Amplified
Polymorphic DNA (RAPD) primers were used to detect
polymorphism between two near isogenic lines NILs (Anza and
Anza+2NS) of wheat and to develop RAPD based molecular
markers for rust resistance gene cluster derived from T.
ventricosum. Polymerase chain reactions were carried out
using standard protocols. All the amplification products
were in the range of 250 to 1000 bp. Thirteen molecular
markers (RAPDs) out of a total of 150 (approximately 8.6%)
were developed for rust resistance gene cluster
Lr37-Sr38-Yr17 and recommendations have been made to
utilize these markers in Pakistani wheat breeding programs
aimed at establishing rust resistant germplasm.