Several disease-resistant recombinants between barley (Hordeum vulgare) and
bulbous barley grass (H. bulbosum) have been obtained in recent years, but
the process of characterization is often laborious and time-consuming. In
order to improve the identification and chromosomal location of introgresse
d chromatin from H, bulbosum into the barley genome, we employed sequential
genomic in situ hybridization (GISH) and fluorescence in situ hybridizatio
n (FISH). GISH enabled us to establish that an introgression was present in
the disease-resistant recombinant line, and the subsequent use of FISH, wi
th a short oligonucleotide sequence as probe, allowed us to locate the intr
ogression on the long arm of barley chromosome 2H. These data were confirme
d using RFLP probes that hybridize to barley chromosome 2HL.