- Ravenscroft, Thomas A;
- Phillips, Jennifer B;
- Fieg, Elizabeth;
- Bajikar, Sameer S;
- Peirce, Judy;
- Wegner, Jeremy;
- Luna, Alia A;
- Fox, Eric J;
- Yan, Yi-Lin;
- Rosenfeld, Jill A;
- Zirin, Jonathan;
- Kanca, Oguz;
- Benke, Paul J;
- Cameron, Eric S;
- Strehlow, Vincent;
- Platzer, Konrad;
- Jamra, Rami Abou;
- Klöckner, Chiara;
- Osmond, Matthew;
- Licata, Thomas;
- Rojas, Samantha;
- Dyment, David;
- Chong, Josephine SC;
- Lincoln, Sharyn;
- Stoler, Joan M;
- Postlethwait, John H;
- Wangler, Michael F;
- Yamamoto, Shinya;
- Krier, Joel;
- Westerfield, Monte;
- Bellen, Hugo J
Purpose
Growth differentiation factor 11 (GDF11) is a key signaling protein required for proper development of many organ systems. Only one prior study has associated an inherited GDF11 variant with a dominant human disease in a family with variable craniofacial and vertebral abnormalities. Here, we expand the phenotypic spectrum associated with GDF11 variants and document the nature of the variants.Methods
We present a cohort of six probands with de novo and inherited nonsense/frameshift (4/6 patients) and missense (2/6) variants in GDF11. We generated gdf11 mutant zebrafish to model loss of gdf11 phenotypes and used an overexpression screen in Drosophila to test variant functionality.Results
Patients with variants in GDF11 presented with craniofacial (5/6), vertebral (5/6), neurological (6/6), visual (4/6), cardiac (3/6), auditory (3/6), and connective tissue abnormalities (3/6). gdf11 mutant zebrafish show craniofacial abnormalities and body segmentation defects that match some patient phenotypes. Expression of the patients' variants in the fly showed that one nonsense variant in GDF11 is a severe loss-of-function (LOF) allele whereas the missense variants in our cohort are partial LOF variants.Conclusion
GDF11 is needed for human development, particularly neuronal development, and LOF GDF11 alleles can affect the development of numerous organs and tissues.