The rhizomania disease is one of the most important diseases
in Iran and some other parts of the world which potentially
could play a role in decreasing sugar yield in fields. One
approach to combat with this disease is the use of
resistance varieties. This varieties have been identified
which are having resistance genes to rhizomania disease
(i.e. Rz1, Rz2). In
order to use these genes in breeding programs (MAS) tagging
these genes with molecular markers is necessary. In our
study, we used infected soil which was provided from
infected fields then greenhouse test was done to identify
resistance and susceptible plants. Extracted DNA from leaves
of resistant and susceptible plants was bulked to provide
two bulks for resistance and susceptible plants.
Three-hundred RAPD primers were used in analysis of the two
bulks and two F2 populations. One population was
obtained from a cross between Holly1-4 as resistance parent
and an annual variety as susceptible plant. The second
population was constructed by crossing between WB42 as
resistance parent and L 261 as susceptible one. Finally
genes were tagged using two RAPD primers and one of the
markers is OP-091150 which is 27 cM apart from
Rz1gene in coupling phase. The second marker
is OP-AN9600 which is 13.7 cM apart from Rz1gene and in repulsion phase.