Abstract

BackgroundThe bone morphogenetic protein (BMP) signaling gradient is central for dorsoventral patterning in amphibian embryos. This gradient is established through the interaction of several BMPs and BMP antagonists and modulators, some secreted by Spemann's organizer, a cluster of cells coordinating embryonic development. Anti-dorsalizing morphogenetic protein (ADMP), a BMP-like transforming growth factor beta ligand, negatively affects the formation of the organizer, although it is robustly expressed within the organizer itself. Previously, we proposed that this apparent discrepancy may be important for the ability of ADMP to scale the BMP gradient with embryo size, but how this is achieved is unclear.ResultsHere we report that ADMP acts in the establishment of the organizer via temporally and mechanistically distinct signals. At the onset of gastrulation, ADMP is required to establish normal organizer-specific gene expression domains, thus displaying a dorsal, organizer-promoting function. The organizer-restricting, BMP-like function of ADMP becomes apparent slightly later, from mid-gastrula. The organizer-promoting signal of ADMP is mediated by the activin A type I receptor, ACVR1 (also known as activin receptor-like kinase-2, ALK2). ALK2 is expressed in the organizer and is required for organizer establishment. The anti-organizer function of ADMP is mediated by ACVRL1 (ALK1), a putative ADMP receptor expressed in the lateral regions flanking the organizer that blocks expansion of the organizer. Truncated ALK1 prevents the organizer-restricting effects of ADMP overexpression, suggesting a ligand-receptor interaction. We also present a mathematical model of the regulatory network controlling the size of the organizer.ConclusionsWe show that the opposed, organizer-promoting and organizer-restricting roles of ADMP are mediated by different receptors. A self-regulating network is proposed in which ADMP functions early through ALK2 to expand its own expression domain, the organizer, and later functions through ALK1 to restrict this domain. These effects are dependent on ADMP concentration, timing, and the spatial localization of the two receptors. This self-regulating temporal switch may control the size of the organizer and the genes expressed within in response to genetic and external stimuli during gastrulation.

Highlights

  • The bone morphogenetic protein (BMP) signaling gradient is central for dorsoventral patterning in amphibian embryos

  • To better understand the function of Anti-dorsalizing morphogenetic protein (ADMP) as a putative BMP during early embryogenesis, we studied its regulatory effects when overexpressed at different levels (32–800 pg injected messenger RNA, mRNA)

  • Embryos injected with increasing amounts of ADMP-capped RNA were analyzed during early gastrula [23]

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Summary

Introduction

The bone morphogenetic protein (BMP) signaling gradient is central for dorsoventral patterning in amphibian embryos. This gradient is established through the interaction of several BMPs and BMP antagonists and modulators, some secreted by Spemann's organizer, a cluster of cells coordinating embryonic development. The organizer secretes a number of BMP antagonists and regulatory proteins to create a low level of BMP signaling on the dorsal side of the embryo, close to the organizer, and shuttle BMP molecules to the ventral side [1, 7,8,9,10,11,12,13]. Multiple proteins have been identified that regulate the availability and stability of BMP4, including Tolloid, a metalloprotease [14], and Sizzled, a ventrally expressed and highly diffusible inhibitor of Tolloid [8, 15]

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