A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1). ...

Spongy degeneration with cerebellar ataxia (SDCA) is a severe neurodegenerative disease with monogenic autosomal recessive inheritance in Malinois dogs, one of the four varieties of the Belgian Shepherd breed. We performed a genetic investigation in six families and seven isolated cases of Malinois dogs with signs of cerebellar dysfunction. Linkage analysis revealed an unexpected genetic heterogeneity within the studied cases. The affected dogs from four families and one isolated case shared a ~1.4 Mb common homozygous haplotype segment on chromosome 38. Whole genome sequence analysis of three... Mehr ...

Verfasser: Schuller, Simone
Dietschi, Elisabeth
Stokar-Regenscheit, Nadine
Henke, Diana
Kleiter, Miriam
Högler, Sandra
Oevermann, Anna
Mauri, Nico
O'Toole, Donal
Leschnik, Michael
Steffen, Frank
Leeb, Tosso
Dietrich, Sara Joëlle
Jagannathan, Vidhya
Herden, Christiane
Bilzer, Thomas
Wiedmer, Michaela
Gurtner, Corinne
Dokumenttyp: Text
Erscheinungsdatum: 2016
Verlag/Hrsg.: Genetics Society of America
Schlagwörter: 590 Animals Zoology / 570 Life sciences; biology / 610 Medicine & health / 630 Agriculture
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-28885563
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://dx.doi.org/10.7892/boris.93473

Spongy degeneration with cerebellar ataxia (SDCA) is a severe neurodegenerative disease with monogenic autosomal recessive inheritance in Malinois dogs, one of the four varieties of the Belgian Shepherd breed. We performed a genetic investigation in six families and seven isolated cases of Malinois dogs with signs of cerebellar dysfunction. Linkage analysis revealed an unexpected genetic heterogeneity within the studied cases. The affected dogs from four families and one isolated case shared a ~1.4 Mb common homozygous haplotype segment on chromosome 38. Whole genome sequence analysis of three affected and 140 control dogs revealed a missense variant in the KCNJ10 gene encoding a potassium channel (c.986T>C; p.Leu329Pro). Pathogenic variants in KCNJ10 were reported previously in humans, mice, and dogs with neurological phenotypes. Therefore, we consider KCNJ10:c.986T>C the most likely candidate causative variant for one subtype of SDCA in Malinois dogs, which we propose to term spongy degeneration with ...