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XB-ART-54282
Elife January 1, 2017; 6

Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish.

Bisgrove BW , Su YC , Yost HJ .


Abstract
Zebrafish Gdf3 (Dvr1) is a member of the TGFβ superfamily of cell signaling ligands that includes Xenopus 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 gdf3 RNA, demonstrating that Gdf3 is required only early in development, beyond which mutants are viable and fertile. Gdf3 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 gdf3 mutants, indicating that Gdf3 functions at the same pathway step as Nodal. Targeting gdf3 and ndr2 RNA to specific lineages indicates that exogenous gdf3 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.

PubMed ID: 29140249
PMC ID: PMC5745076
Article link: Elife
Grant support: [+]
Genes referenced: acvr1 acvr1b evx1 foxa2 gdf1 gdf3 gsc hand2 lefty myod1 nodal nodal1 otx2 sox17b.1 stk38 stk38l


Article Images: [+] show captions
References [+] :
Andersson, Synergistic interaction between Gdf1 and Nodal during anterior axis development. 2006, Pubmed


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