L. Sanchez et al., CLONAL ANALYSIS IN HYBRIDS BETWEEN DROSOPHILA-MELANOGASTER AND DROSAPHILA SIMULANS, Roux's archives of developmental biology, 204(2), 1994, pp. 112-117
We have analysed the viability of cellular clones induced by mitotic r
ecombination in Drosophila melanogaster/D. simulans hybrid females dur
ing larval growth. These clones contain a portion of either melanogast
er or simulans genomes in homozygosity. Analysis has been carried out
for the X and the second chromosomes, as well as for the 3L chromosome
ann. Clones were not found in certain structures, and in others they
appeared in a very low frequency. Only in abdominal tergites was a sig
nificant number of clones observed, although their frequency was lower
than in melanogaster abdomens. The bigger the portion of the genome t
hat is homozygous, the less viable is the recombinant melanogaster/sim
ulans hybrid clone. The few clones that appeared may represent cases i
n which mitotic recombination took place in distal chromosome interval
s, so that the clones contained a small portion of either melanogaster
or simulans chromosomes in homozygosity. Moreover, Lhr, a gene of D.
simulans that suppresses the lethality of male and female melanogaster
/simulans hybrids, does not suppress the lethality of the recombinant
melanogaster/simulans clones. Thus, it appears that there is not just
a single gene, but at least one per tested chromosome arm (and maybe m
ore) that cause hybrid lethality. Therefore, the two species, D. melan
ogaster and D. simulans, have diverged to such a degree that the absen
ce of part of the genome of one species cannot be substituted by the c
orresponding part of the genome of the other, probably due to the form
ation of co-adapted gene complexes in both species following their div
ergent evolution after speciation. The disruption of those co-adapted
gene complexes would cause the lethality of the recombinant hybrid clo
nes.