RESUMEN
Nodal signalling is essential for many developmental events during vertebrate development, including the establishment of left-right asymmetry, of dorsoventral axis of the central nervous system, and endoderm and mesoderm formation. The zebrafish TGFbeta-related type I receptor, TARAM-A (Tar), is expressed in the prospective mesendodermal territory and, when activated, can transfate early blastomeres into endoderm, suggesting that Nodal and Tar may represent similar signalling pathways. We have analysed the functional relationships between those two pathways in zebrafish. We first demonstrate that tar and the zebrafish nodal genes cyc and sqt functionally interact. We also show that a dominant-negative isoform of Tar, TarMR, interferes specifically with the function of Cyc and Sqt in vitro, but does not interfere with the function of BMP2, another TGFbeta-related molecule. TarMR interferes also with Nodal signalling in vivo since it enhances the phenotype of embryos with weakened Nodal signalling. Overexpression of tarMR in wild-type embryos interfered with the formation of endoderm-derived structures. Conversely, overexpression of tar enlarged the presumptive mesendodermal region at the onset of gastrulation. Together, our results point to Tar as an essential factor for endoderm formation and an important modulator of Nodal signalling, potentially representing one of the Nodal receptors. (c)2001 Elsevier Science.
Asunto(s)
Tipificación del Cuerpo/fisiología , Endodermo/fisiología , Regulación del Desarrollo de la Expresión Génica , Mesodermo/fisiología , Proteínas Serina-Treonina Quinasas , Receptores de Factores de Crecimiento Transformadores beta/fisiología , Transducción de Señal/fisiología , Factor de Crecimiento Transformador beta/fisiología , Proteínas de Pez Cebra , Activinas/metabolismo , Animales , Biomarcadores , Tipificación del Cuerpo/genética , Proteínas Morfogenéticas Óseas/fisiología , Embrión no Mamífero/fisiología , Genes Dominantes , Proteínas de Homeodominio/genética , Proteínas de Homeodominio/fisiología , Péptidos y Proteínas de Señalización Intracelular , Mutagénesis , Proteína Nodal , Ligandos de Señalización Nodal , Fenotipo , Receptores de Factores de Crecimiento Transformadores beta/genética , Proteínas Recombinantes de Fusión/fisiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Transducción de Señal/genética , Factores de Transcripción/genética , Factores de Transcripción/fisiología , Factor de Crecimiento Transformador beta/genética , Pez Cebra/embriología , Pez Cebra/genéticaRESUMEN
Endoderm originates from a large endomesodermal field requiring Nodal signalling. The mechanisms that ensure segregation of endoderm from mesoderm are not fully understood. We first show that the timing and dose of Nodal activation are crucial for endoderm formation and the endoderm versus mesoderm fate choice, because sustained Nodal signalling is required to ensure endoderm formation but transient signalling is sufficient for mesoderm formation. In zebrafish, downstream of Nodal signals, three genes encoding transcription factors (faust, bonnie and clyde and the recently identified gene casanova) are required for endoderm formation and differentiation. However their positions within the pathway are not completely established. In the present work, we show that casanova is the earliest specification marker for endodermal cells and that its expression requires bonnie and clyde. Furthermore, we have analysed the molecular activities of casanova on endoderm formation and found that it can induce endodermal markers and repress mesodermal markers during gastrulation, as well as change the fate of marginal blastomeres to endoderm. Overexpression of casanova also restores endoderm markers in the absence of Nodal signalling. In addition, casanova efficiently restores later endodermal differentiation in these mutants, but this process requires, in addition, a partial activation of Nodal signalling.
