Analysis of the requirement of GATA-binding factors for inducible
CecA1 expression in the yolk and epidermis,
respectively. Anterior is to the left, and all embryos are in lateral
view with dorsal up, except for E which is in ventral
view. Embryos were injected with LPS before (A,
C, and E) or 12 h after
(B, D, and F) egg laying
to induce CecA1 expression in the yolk or in the
epidermis, respectively. (A–B) β-gal
staining in A16 CecA1-lacZ embryos with a
mutated GATA site. No expression is observed in the yolk
(A), whereas expression in the epidermis is strong
(B). (C–F) β-gal
expression in A10 CecA1-lacZ embryos in
srp6G mutant background. No
CecA1 expression could be detected in the yolk of
homozygous srp6G embryos (C)
but is evident clearly in individual cells and in patches of cells in
the epidermis (D). The development of the
srp6G embryos (C and
D) is arrested, and the embryos do not complete
germ-band retraction and dorsal closure as their heterozygous siblings
(E and F). In embryos heterozygous for
srp6G and for the
ftz-lacZ blue balancer, the β-gal
staining is evident both from the CecA1 promoter
(arrows) in the yolk (E and F), in the
epidermis (F), and from the ftz promoter
(arrowheads) in a weak stripe in the anterior part of the embryo
(E) and in the ventral nerve chord (E and
F; refs. 23 and 24).