Dosch R et al. (1997), Bmp-4 acts as a morphogen in dorsoventral mesod...

XB-ART-16423

Development 1997 Jun 01;12412:2325-34. doi: 10.1242/dev.124.12.2325.

Show Gene links Show Anatomy links

Bmp-4 acts as a morphogen in dorsoventral mesoderm patterning in Xenopus.

Dosch R , Gawantka V , Delius H , Blumenstock C , Niehrs C .

???displayArticle.abstract???
The marginal zone is a ring of tissue that gives rise to a characteristic dorsoventral pattern of mesoderm in amphibian embryos. Bmp-4 is thought to play an important role in specifying ventral mesodermal fate. Here we show (1) that different doses of Bmp-4 are sufficient to pattern four distinct mesodermal cell types and to pattern gene expression in the early gastrula marginal zone into three domains, (2) that there is a graded requirement for a Bmp signal in mesodermal patterning, and (3) that Bmp-4 has long-range activity which can become graded in the marginal zone by the antagonizing action of noggin. The results argue that Bmp-4 acts as a morphogen in dorsoventral patterning of mesoderm.

???displayArticle.pubmedLink??? 9199359
???displayArticle.link??? Development

Species referenced: Xenopus
Genes referenced: bmp4 chrd myf5 myod1 nog smad1 ventx1 ventx1.2 ventx2 ventx2.2

???attribute.lit??? ???displayArticles.show???

	Fig. 1. Different doses of Bmp-4 are necessary and sufficient for patterning terminal differentiation of mesoderm. 4-cell-stage embryos were microinjected into all blastomeres with the indicated amount of mRNA. Dorsal marginal zones (DMZ) were excised (encompassing the 60Â° dorsal lip only) from embryos injected with Bmp-4 mRNA and ventral marginal zones (VMZ) were excised from embryos injected with DmTFR11. Note the successive peaks of differentiation. For each injected dose at least 12 explants were analyzed for the presence of the indicated marker tissues, the frequency of which is given in percent. Identification of welldifferentiated tissues was by morphological criteria by two individuals scoring independently. 100% is the total number of explants scored and each individual explant may contain multiple tissues. For the highest dose of injected DmTFR11 mRNA, 4-cell embryos were only injected into two ventral blastomeres in such a way that the injections left little scars. This permitted safe identification of the ventral side even in gastrula embryos that contained secondary dorsal lips.
	Fig. 2. XMyf-5 is a molecular marker for the dorsolateral marginal zone. Whole-mount in situ hybridisations of XMyf-5, XMyoD, Xvent-1, Xvent-2 and noggin. Xmyf-5 and XMyoD expression at the indicated stages are shown in the top two panels. Stage 10+ embryos are in vegetal view with the dorsal side facing up, stage 12 embryos in dorsal view with anterior facing left. The XMyf-5 expression domain always remains dorsolateral until late gastrulation, while XmyoD is expressed additionally in the lateroventral domain of the gastrula and the circumblastoporal collar in stage 12 embryos. Lower panel shows stage 10+ gastrulae. Note that the expression of Xvent-1 is nested within the domain of Xvent-2 expression. These expression patterns molecularly define a dorsal, dorsolateral and lateroventral domain, as shown schematically in the lower right. The domains correspond to expression of noggin (blue), XMyf-5 (white) and Xvent-1 (red). All embryos are shown in vegetal view with the dorsal side up.
	Fig. 3. Different doses of Bmp-4 are necessary and sufficient for patterning of the marginal zone. 4-cell-stage embryos were microinjected into all blastomeres with either 50 (low) or 150 pg (high) Bmp-4 mRNA, or either 100 (low) or 1000 pg (high) dominant negative Bmp receptor (DmTFR11) mRNA per blastomere as indicated. Embryos were processed for whole-mount in situ hybridisation at stage 10+. All embryos are shown in vegetal view with the dorsal side up. Typically, two sets of titration experiments by microinjections were carried out with two-fold dose increments and at least five embryos per experiment. Of a population of injected embryos, a representative specimen is shown for the respective dose. For simplicity, only key doses are displayed (wt, uninjected controls).
	Fig. 4. Dose-dependent modulation of Bmp-4 activity by noggin. (A) 4-cell-stage embryos were microinjected into all blastomeres with noggin or Bmp-4 mRNA or both with the indicated dose in ng per blastomere. Dorsal (DMZ, top) or ventral (VMZ, bottom) marginal zones were excised at the gastrula stage and cultured until sibling embryos reached late gastrula. Explants were analyzed for expression of EF1-a, gsc and Xvent-1, as indicated. WE, whole embryo; -RT, -reverse transcription. (B) 4-cell-stage embryos were microinjected into all blastomeres with 30 (low) or 500 pg (high) noggin mRNA per blastomere. Embryos were processed for wholemount in situ hybridisation at stage 10+ with the probes indicated. All embryos are shown in vegetal view with the dorsal side up.
	Fig. 5. Direct and long-range action of Bmp-4 and noggin. (A) (Top) 32-cell-stage embryos were microinjected with 0.2 ng b-galactosidase lineage tracer mRNA containing a nuclear localization signal and either without (lacZ) or with 30 pg Bmp-4 or 500 pg Xsmad1 (XMad-1) mRNA as indicated into two marginal zone blastomeres, followed by treatment with LiCl. Embryos were processed for whole-mount in situ hybridisation at stage 10+ with Xvent-1. Note that Xvent-1 expression extends beyond the injected cells (light blue nuclei) in the Bmp-4- injected embryo, while it is restricted to the b-galactosidase-positive cells in Xsmad1-injected embryos. Embryos are shown in lateral view with the animal side up. The insets show a magnification of the highlighted area. (Bottom) 4-cell-stage embryos were uninjected (control) or microinjected into all blastomeres with Bmp-4 or Xsmad1 mRNA. Note that the phenotype of both Bmp-4- as well as Xsmad1-microinjected embryos is complete BauchstÃ¼ck-type ventralization. (B) 32-cell-stage embryos were microinjected with 0.2 ng b-galactosidase lineage tracer mRNA containing a nuclear localization signal and either without (lacZ) or with 25 pg (low) or 100 pg (high) noggin mRNA, as indicated, into two marginal zone blastomeres. Embryos were processed for whole-mount in situ hybridisation at stage 10+ with Xvent-1 or Xvent-2 as indicated. Note that the Xvent-1 and Xvent-2 repression halos extend beyond the injected cells (light blue nuclei) in the noggin-injected embryos and that the size of the halo is dose dependent. Embryos are shown in lateral view with the animal side up.