Genetic interactions between tup, tin, pnr
and Doc. The cardiac phenotypes in transheterozygotic
Drosophila embryos demonstrate that tup interacts
genetically with all three factors. The phenotypes were compared with those of
the cardiac markers in single heterozygotes, and were evaluated statistically
for Dmef2 (see Tables 1 and
2). (A-D) Dmef2
expression in the wild type (A) and in embryos transheterozygotic for
tupisl-1 and pnrVX6 (B),
tupisl-1 and tin346 (C),
tupisl-1 and Df(3L)DocA (D). Dorsal views of
embryos at stage 15/16 are shown. Arrows point to gaps in the myocardial rows
of the dorsal vessel. (E,F) Pnr is reduced in
tup/tin transheterozygotic embryos (arrows in F). A lateral
view of a stage 11 embryo is shown. (G-I) Tin expression in the wild
type (G), and in embryos transheterozygotic for tup and pnr
(H), and tup and DocA (I). Reduced Tin expression is seen in
both cases (arrows in H,I). Dorsal views of stage 14 embryos are shown.