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Fig. 6. BMP responsiveness of SR3/CAR3 and cardiac expression of a CAR3-driven
transgene requires intact binding sites for transcription factor YY1. (A)
Sequence of SR3 region encompassing site D (blue box) and SBE3 (green box).
Sense and antisense YY1 consensus binding sites are shown above putative
YY1-binding sites within SR3. Point mutations in putative YY1 binding sites A
and B are shown in red below their cognate nucleotides. (B) YY1 binds to SR3.
EMSA with oligos encoding either WT SR3 (lanes 1 and 5) or SR3 with mutations
in putative YY1-binding site A (lane 2), site B (lane 3) or sites A+B (lane 4)
with either P19 cell nuclear extract (top panel), whole cell extracts from
day3 (HH Stage 24) chick hearts (middle panel) or purified HA-tagged YY1
protein (lower panel). Point mutation of the YY1 consensus binding site B in
the SR3 oligomer significantly decreased or abolished DNA-binding activities
in all samples (lane 3), as did mutations of both sites A and B (lane 4).
Anti-YY1 polyclonal antibody added to the EMSA disrupted the interaction of
factors in both P19 cells and day 3 chick hearts with the SR3 oligomer (lane
5). (C) Point mutation of the YY1 consensus site B in the context of an
Nkx2.5-lux-CAR3 reporter (schematized at top) results in loss of BMP response
in P19 cells. Results are shown in duplicate for wild-type Nkx2.5-lux-CAR3
(left) and Nkx2.5-lux-CAR3 mutB (right). (D-G) YY1-binding sites are required
for CAR3-driven transgene expression in the heart. Representative X-gal
staining patterns are shown for transgenic mice embryos containing
Nkx2.5-lacZ-CAR3 mut B (shown in D). lacZ expression is
abrogated at all stages assayed, indicating a requirement for YY1-binding
sites in CAR3 to drive transgene expression in the heart (compare with the
robust cardiac expression of the parental Nkx2.5-lacZ-CAR3 construct
in Fig. 2D-F). Embryonic stages
are shown in the lower left-hand corner. Results are representative of 3/3
E7.5 and 5/5 E10.5 transgenic embryos. Abbreviations are as in previous
figures.