| First Author | Motta M | Year | 2021 |
| Journal | Am J Hum Genet | Volume | 108 |
| Issue | 11 | Pages | 2112-2129 |
| PubMed ID | 34626534 | Mgi Jnum | J:325031 |
| Mgi Id | MGI:6857925 | Doi | 10.1016/j.ajhg.2021.09.007 |
| Citation | Motta M, et al. (2021) SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype. Am J Hum Genet 108(11):2112-2129 |
| abstractText | Upregulated signal flow through RAS and the mitogen-associated protein kinase (MAPK) cascade is the unifying mechanistic theme of the RASopathies, a family of disorders affecting development and growth. Pathogenic variants in more than 20 genes have been causally linked to RASopathies, the majority having a dominant role in promoting enhanced signaling. Here, we report that SPRED2 loss of function is causally linked to a recessive phenotype evocative of Noonan syndrome. Homozygosity for three different variants-c.187C>T (p.Arg63( *)), c.299T>C (p.Leu100Pro), and c.1142_1143delTT (p.Leu381Hisfs( *)95)-were identified in four subjects from three families. All variants severely affected protein stability, causing accelerated degradation, and variably perturbed SPRED2 functional behavior. When overexpressed in cells, all variants were unable to negatively modulate EGF-promoted RAF1, MEK, and ERK phosphorylation, and time-course experiments in primary fibroblasts (p.Leu100Pro and p.Leu381Hisfs( *)95) documented an increased and prolonged activation of the MAPK cascade in response to EGF stimulation. Morpholino-mediated knockdown of spred2a and spred2b in zebrafish induced defects in convergence and extension cell movements indicating upregulated RAS-MAPK signaling, which were rescued by expressing wild-type SPRED2 but not the SPRED2(Leu381Hisfs)( *)(95) protein. The clinical phenotype of the four affected individuals included developmental delay, intellectual disability, cardiac defects, short stature, skeletal anomalies, and a typical facial gestalt as major features, without the occurrence of the distinctive skin signs characterizing Legius syndrome. These features, in part, characterize the phenotype of Spred2(-/-) mice. Our findings identify the second recessive form of Noonan syndrome and document pleiotropic consequences of SPRED2 loss of function in development. |
