Gene defect in ectodermal dysplasia implicates a death domain adapter in development

Denis J. Headon, Stephanie A. Emmal, Betsy M. Ferguson, Abigail S. Tucker, Monica J. Justice, Paul T. Sharpe, Jonathan Zonana, Paul A. Overbeek

Research output: Contribution to journalArticlepeer-review

303 Scopus citations


Members of the tumour-necrosis factor receptor (TNFR) family that contain an intracellular death domain initiate signalling by recruiting cytoplasmic death domain adapter proteins. Edar is a death domain protein of the TNFR family that is required for the development of hair, teeth and other ectodermal derivatives. Mutations in Edar - or its ligand, Eda - cause hypohidrotic ectodermal dysplasia in humans and mice. This disorder is characterized by sparse hair, a lack of sweat glands and malformation of teeth. Here we report the identification of a death domain adapter encoded by the mouse crinkled locus. The crinkled mutant has an hypohidrotic ectodermal dysplasia phenotype identical to that of the edar (downless) and eda (Tabby) mutants. This adapter, which we have called Edaradd (for Edar-associated death domain), interacts with the death domain of Edar and links the receptor to downstream signalling pathways. We also identify a missense mutation in its human orthologue, EDARADD, that is present in a family affected with hypohidrotic ectodermal dysplasia. Our findings show that the death receptor/adapter signalling mechanism is conserved in developmental, as well as apoptotic, signalling.

Original languageEnglish (US)
Pages (from-to)913-916
Number of pages4
Issue number6866
StatePublished - Dec 20 2001

ASJC Scopus subject areas

  • General


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