Maternal Gdf3 is an Obligatory Cofactor in Nodal Signaling for Embryonic Axis Formation in Zebrafish

Overview

Journal Elife

Specialty Biology

Date 2017 Nov 16

PMID 29140249

Citations 19

Authors

Brent W Bisgrove

Yi-Chu Su

H Joseph Yost

Affiliations

Soon will be listed here.

Abstract

Zebrafish Gdf3 (Dvr1) is a member of the TGFβ superfamily of cell signaling ligands that includes Vg1 and mammalian Gdf1/3. Surprisingly, engineered homozygous mutants in zebrafish have no apparent phenotype. Elimination of Gdf3 in oocytes of maternal-zygotic mutants results in embryonic lethality that can be fully rescued with RNA, demonstrating that Gdf3 is required only early in development, beyond which mutants are viable and fertile. mutants are refractory to Nodal ligands and Nodal repressor Lefty1. Signaling driven by TGFβ ligand Activin and constitutively active receptors Alk4 and Alk2 remain intact in mutants, indicating that Gdf3 functions at the same pathway step as Nodal. Targeting and RNA to specific lineages indicates that exogenous is able to fully rescue mutants only when co-expressed with endogenous Nodal. Together, these findings demonstrate that Gdf3 is an essential cofactor of Nodal signaling during establishment of the embryonic axis.

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