There are approximately 25 000 species in the division Teleostei and most a
rc believed to have arisen during a relatively short period of time ca. 200
Myr ago. The discovery of 'extra' Hox gene clusters in zebrafish (Danio re
rio), medaka (Oryzias latipes), and pufferfish (Fugu rubripes), has led to
the hypothesis that genome duplication provided the genetic raw material ne
cessary for the telcost radiation. We identified 27 groups of orthologous g
enes which included one gene from man, mouse and chicken, one or two genes
from tetraploid Xenopus and two genes from zebrafish. A genome duplication
in the ancestor of teleost fishes is the most parsimonious explanation for
the observations that for 15 of these genes, the two zebrafish orthologues
are sister sequences in phylogenies that otherwise match the expected organ
ismal tree, the zebrafish gene pairs appear to have been formed at approxim
ately the same time, and are unlinked. Phylogenies of nine genes differ a l
ittle from the tree predicted by the fish-specific genome duplication hypot
hesis: one tree shows a sister sequence relationship for the zebrafish gene
s but differs slightly from the expected organismal tree and in eight trees
, one zebrafish gene is the sister sequence to a clade which includes the s
econd zebrafish gene and orthologues from Xenopus, chicken, mouse and man.
For these nine gene trees, deviations from the predictions of the fish-spec
ific genome duplication hypothesis are poorly supported. The two zebrafish
orthologues for each of the three remaining genes are tightly linked and ar
e, therefore, unlikely to have been formed during a genome duplication even
t. We estimated that the unlinked duplicated zebrafish genes are between 30
0 and 450 Myr. Thus, genome duplication could have provided the genetic raw
material for teleost radiation. Alternatively, the loss of different dupli
cates in different populations (i.e. 'divergent resolution') may have promo
ted speciation in ancient teleost populations.