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Fig. 3. Regulation of endoderm genes by Nodal proteins, Mixer and Sox17.
(A) The expression of the 301 endoderm-enriched sequences was
determined by microarray analysis at stage 11 in three experimental
conditions. (1) Nodal-, embryos where nodal signaling was inhibited by
injection of Cerberus-S RNA (1 ng/embryo). (2) Mixer-, embryos
injected with Mixer antisense morpholino oligos (40 ng/embryo). (3) Sox17-,
embryos injected with antisense morpholino oligos to Sox17
1 +
Sox17
2 + Sox17ß (20 ng each/embryo). The average intensity,
normalized to stage 11 whole embryo (We) is shown on a log scale. An, animal
cap ectoderm; Veg, endoderm enriched vegetal tissue; Eq, mesendoderm enriched
equatorial tissue. The yellow lines indicate the 1.4-fold change threshold
from the control. (B) Hierarchical clustering indicates which
conditions have the most similar expression profiles. Low expression is
indicated in blue and high expression in red. A transcript was considered
`regulated' in a given condition if its expression was more than 1.4-fold
changed from whole embryo control. (C) The Venn diagram shows that
based on this 1.4-fold criteria, 112/301 endoderm transcripts are Nodal
regulated, 168/301 are Mixer regulated and 100/301 are Sox17 regulated, with a
total of 223/301 endoderm transcripts that are regulated by either Nodal
proteins Mixer or Sox17. Only 36/301 of transcripts (white) are regulated in a
manner consistent with the simple linear model of endoderm development.