Abstract
In these studies, we have taken advantage of a transient transgenic strategy in Xenopus embryos to demonstrate that BMP signaling is required in vivo for heart formation in vertebrates. Ectopic expression of dominant negative Type I (tALK3) or Type II (tBMPRII) BMP receptors in developing Xenopus embryos results in reduction or absence of heart formation. Additionally, blocking BMP signaling in this manner downregulates expression of XNkx2-5, a homeobox gene required for cardiac specification, prior to differentiation. Notably, however, initial expression of XNkx2-5 is not affected. Mutant phenotypes can be rescued by co-injection of mutant with wild-type receptors or co-injection of mutant receptors with XSmad1, a downstream mediator of BMP signaling. Whole-mount in situ analyses indicate that ALK3 and XSmad1 are coexpressed in cardiogenic regions. Together, our results demonstrate that BMP signaling is required for maintenance of XNkx2-5 expression and heart formation and suggest that ALK3, BMPRII, and XSmad1 may mediate this signaling. (C) 2000 Academic Press.
Original language | English |
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Pages (from-to) | 226-237 |
Number of pages | 12 |
Journal | Developmental Biology |
Volume | 224 |
Issue number | 2 |
DOIs | |
State | Published - 15 Aug 2000 |
Externally published | Yes |
Keywords
- ALK3
- BMP
- BMPRII
- Cardiogenesis
- Smad1
- Tinman homologues
- Truncated BMPR