If loci are randomly distributed on a physical map, the density of mar
kers on a genetic map will be inversely proportional to recombination
rate. First proposed by MARY LYON, We have used this idea to estimate
recombination rates from the Drosophila melanogaster linkage map. Thes
e results were compared with results of two other studies that estimat
ed regional recombination rates in D. melanogaster using both physical
and genetic maps. The three methods were largely concordant in identi
fying large-scale genomic patterns of recombination. The marker densit
y method was then applied to the Mus musculus microsatellite linkage m
ap. The distribution of microsatellites provided evidence for heteroge
neity in recombination rates. Centromeric regions for several mouse ch
romosomes had significantly greater numbers of markers than expected,
suggesting that recombination rates were lower in these regions. In co
ntrast, most telomeric regions contained significantly fewer markers t
han expected. This indicates that recombination rates are elevated at
the telomeres of many mouse chromosomes and is consistent with a compa
rison of the genetic and cytogenetic maps in these regions. The densit
y of markers on a genetic map may provide a generally useful way to es
timate regional recombination rates in species for which genetic, but
not physical, maps are available.