Three principal approaches are used in our laboratory to analyze plant
genomes: (i) The construction of high density molecular maps using a
refined microdissection procedure to construct chromosomal and subchro
mosomal libraries. (ii) Synteny analysis: The Aegilops-based deletion
mapping system in wheat that has led to the construction of a high-den
sity physical consensus map of wheat. The integration of wheat, barley
and oat RFLP markers has proven the colinearity between the wheat A-,
B- and D-genomes, the H-genome of barley, and the E-genome of Agropyr
on. (iii) Gene mapping in situ, and chromosomes at high resolution: Se
nsitivity enhancement of fluorescence in situ hybridization (FISH) and
an efficient preparation of plant chromosomes has been developed. A t
andemly amplified repetitive sequence element from microdissected barl
ey chromosomes has enabled the karyotyping of individual Gramineae gen
omes in a single step. These sequences are also useful for double or t
riple hybridization-experiments. The low copy genes for the: storage p
roteins Sec-1 and Hor-B have been topographically mapped on the satell
ite of chromosome 1R of rye and the syntenic locus on barley chromosom
e 1H.