We have used clones of 17 single-copy human DNA sequences to analyze t
heir counterparts in the genome of the domestic dog by heterologous hy
bridization. Ten of the 17 sequences represented anchor loci proposed
for comparative mammalian mapping, Eight of 17 human clones (including
three of the anchor loci) gave clear hybridization signals when used
with Southern blots of canine DNA, Five of these eight (including two
anchor loci) showed diallelic restriction fragment length polymorphism
s in a large kindred of Brittany spaniels and could be used for segreg
ation studies, Several probes chosen from different human chromosomes
also were unlinked in the dog, By contrast, linkage was found between
the canine counterparts of the closely linked human serum amyloid A ge
ne family, Three markers linked on human chromosome II appeared not to
be syntenic in the dog, DNA markers linked to various human genetic n
euromuscular diseases were not linked to hereditary canine spinal musc
ular atrophy which segregates in this kindred, However, there was evid
ence of possible linkage of this disorder with a canine counterpart of
the tyrosinase gene, Segregation studies using heterologous single-co
py DNA probes can be performed in dogs, but the level of inbreeding ma
y reduce heterogeneity and limit the power of the analysis.