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September 12, 2008Science158 citations

A Mutation in Hairless Dogs Implicates FOXI3 in Ectodermal Development

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CDCord DrögemüllerEKElinor K. KarlssonMHMarjo K. Hytönen

Key Points

  • This research investigates the genetic basis of ectodermal dysplasia in hairless dog breeds.
  • Conducted genomewide association analysis to identify mutations.
  • Mapped CED mutation to a 102-kilo-base pair interval on chromosome 17.
  • Analyzed mutation within the FOXI3 coding sequence in affected dog breeds.
  • Identified frameshift mutation in FOXI3 among hairless dogs.
  • Mapped mutation linked to canine ectodermal dysplasia phenotype.
  • FOXI3 is determined to be a key regulator of ectodermal development.

Abstract

Mexican and Peruvian hairless dogs and Chinese crested dogs are characterized by missing hair and teeth, a phenotype termed canine ectodermal dysplasia (CED). CED is inherited as a monogenic autosomal semidominant trait. With genomewide association analysis we mapped the CED mutation to a 102-kilo-base pair interval on chromosome 17. The associated interval contains a previously uncharacterized member of the forkhead box transcription factor family (FOXI3), which is specifically expressed in developing hair and teeth. Mutation analysis revealed a frameshift mutation within the FOXI3 coding sequence in hairless dogs. Thus, we have identified FOXI3 as a regulator of ectodermal development.

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Cite This Study

Drögemüller et al. (2008) studied this question.

synapsesocial.com/papers/6a220ee900d082f62f96ff19https://doi.org/10.1126/science.1162525
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