W23
Department of Animal Breeding and Genetics, Box 7023, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden
Chromosome microdissection in horse (ECA) has as yet been carried out
only for ECA1 (Millon et al., unpublished). The library thus constructed
has helped in adding markers to the equine gene map. Since then, the
technique has not been exploited to the advantage of the horse gene
mapping efforts. During the recent past, we have successfully
microdissected some whole chromosomes and arms of equine chromosomes
(ECA1p, ECA1q, ECA2, ECA3 and ECA12). Hybridization of the DOP-PCR
amplified and labelled painting probes generated after microdissection,
back to equine metaphase chromosomes, show that the probes are true to
their origin. Libraries are being constructed for these segments/chromosomes.
Attempts are also underway to add five more equine
chromosomes to this group. The latter primarily include those
chromosomes where no markers have as yet been mapped. It is envisaged
that the libraries thus produced will be used to generate markers in an
orderly way, by concentrating on individual horse chromosomes.