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A TAC3 Missense Variant in a Domestic Shorthair Cat with Testicular Hypoplasia and Persistent Primary Dentition.
Hug, Petra; Kern, Patricia; Jagannathan, Vidhya; Leeb, Tosso.
Afiliación
  • Hug P; Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland. petra.hug@vetsuisse.unibe.ch.
  • Kern P; Tierarztpraxis Spiegelberg AG, 4566 Halten, Switzerland. info@tierarztpraxis-spiegelberg.ch.
  • Jagannathan V; Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland. vidhya.jagannathan@vetsuisse.unibe.ch.
  • Leeb T; Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001 Bern, Switzerland. tosso.leeb@vetsuisse.unibe.ch.
Genes (Basel) ; 10(10)2019 10 14.
Article en En | MEDLINE | ID: mdl-31615056
A single male domestic shorthair cat that did not complete puberty was reported. At four years of age, it still had primary dentition, testicular hypoplasia, and was relatively small for its age. We hypothesized that the phenotype might have been due to an inherited form of hypogonadotropic hypogonadism (HH). We sequenced the genome of the affected cat and compared the data to 38 genomes from control cats. A search for private variants in 40 candidate genes associated with human HH revealed a single protein-changing variant in the affected cat. It was located in the TAC3 gene encoding tachykinin 3, a precursor protein of the signaling molecule neurokinin B, which is known to play a role in sexual development. TAC3 variants have been reported in human patients with HH. The identified feline variant, TAC3:c.220G>A or p.(Val74Met), affects a moderately conserved region of the precursor protein, 11 residues away from the mature neurokinin B sequence. The affected cat was homozygous for the mutant allele. In a cohort of 171 randomly sampled cats, 169 were homozygous for the wildtype allele and 2 were heterozygous. These data tentatively suggest that the identified TAC3 variant might have caused the suppression of puberty in the affected cat.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diente Primario / Taquicininas / Enfermedades de los Gatos / Mutación Missense / Hipogonadismo Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Genes (Basel) Año: 2019 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diente Primario / Taquicininas / Enfermedades de los Gatos / Mutación Missense / Hipogonadismo Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Genes (Basel) Año: 2019 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Suiza