The extent of genetic degeneration of the neo-Y chromosome of Drosophi
la americana americana has been investigated. Three loci, coding for t
he enzymes enolase, phosphoglycerate kinase and alcohol dehydrogenase,
have been localized to chromosome 4 of D. a. americana, which forms t
he neo-Y and neo-X chromosomes. Crosses between D. a. americana and D.
virilis or D. montana showed that the loci coding for these enzymes c
arry active alleles on the neo-Y chromosome in all wild-derived strain
s of americana that were tested. Intercrosses between a genetically ma
rked stock of virilis and strains of americana were carried out, creat
ing F-3 males that were homozygous for sections of the neo-Y chromosom
e. The sex ratios in the F-3 generation of the intercrosses showed tha
t no lethal alleles have accumulated on any of the neo-Y chromosomes t
ested. There was evidence for more minor reductions in fitness, but th
is seems to be mainly caused by deleterious alleles that are specific
to each strain. A similar picture was provided by examination of the s
egregation ratios of two marker genes among the F-3 progeny. Overall,
the data suggest that the neo-Y chromosome has undergone very little d
egeneration, certainly not to the extent of having lost the functions
of vital genes. This is consistent with the recent origin of the neo-Y
and neo-X chromosomes, and the slow rates at which the forces that ca
use Y chromosome degeneration are likely to work.