TY - JOUR T1 - <em>Cdon</em> mutation and fetal alcohol converge on Nodal signaling in a mouse model of holoprosencephaly JF - bioRxiv DO - 10.1101/2020.04.30.070870 SP - 2020.04.30.070870 AU - Mingi Hong AU - Annabel Christ AU - Anna Christa AU - Thomas E. Willnow AU - Robert S. Krauss Y1 - 2020/01/01 UR - http://biorxiv.org/content/early/2020/06/24/2020.04.30.070870.abstract N2 - Holoprosencephaly (HPE), a defect in midline patterning of the forebrain and midface, arises ~1 in 250 conceptions. It is associated with predisposing mutations in the Nodal and Hedgehog (HH) pathways, with penetrance and expressivity graded by genetic and environmental modifiers, via poorly understood mechanisms. CDON is a multifunctional co-receptor, including for the HH pathway. In mice, Cdon mutation synergizes with fetal alcohol exposure, producing HPE phenotypes closely resembling those seen in humans. We report here that, unexpectedly, Nodal, not HH, signaling is the point of synergistic interaction between Cdon mutation and fetal alcohol. Window-of-sensitivity, genetic, and in vitro findings are consistent with a model whereby brief exposure of Cdon mutant embryos to ethanol during gastrulation transiently and partially inhibits Nodal pathway activity, with consequent effects on downstream HH signaling during midline patterning. These results illuminate mechanisms of gene-environment interaction in a multifactorial model of a common birth defect.Competing Interest StatementThe authors have declared no competing interest. ER -