A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).

Dandy-Walker-like malformation (DWLM) is the result of aberrant brain development and mainly characterized by cerebellar hypoplasia. DWLM affected dogs display a non-progressive cerebellar ataxia. Several DWLM cases were recently observed in the Eurasier dog breed, which strongly suggested a monogen...

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Main Authors: Martina Gerber, Andrea Fischer, Vidhya Jagannathan, Michaela Drögemüller, Cord Drögemüller, Martin J Schmidt, Filipa Bernardino, Eberhard Manz, Kaspar Matiasek, Kai Rentmeister, Tosso Leeb
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4323105?pdf=render
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spelling doaj-4dbb5d38ad114cc290825a117af1fdde2020-11-24T21:23:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01102e010891710.1371/journal.pone.0108917A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).Martina GerberAndrea FischerVidhya JagannathanMichaela DrögemüllerCord DrögemüllerMartin J SchmidtFilipa BernardinoEberhard ManzKaspar MatiasekKai RentmeisterTosso LeebDandy-Walker-like malformation (DWLM) is the result of aberrant brain development and mainly characterized by cerebellar hypoplasia. DWLM affected dogs display a non-progressive cerebellar ataxia. Several DWLM cases were recently observed in the Eurasier dog breed, which strongly suggested a monogenic autosomal recessive inheritance in this breed. We performed a genome-wide association study (GWAS) with 9 cases and 11 controls and found the best association of DWLM with markers on chromosome 1. Subsequent homozygosity mapping confirmed that all 9 cases were homozygous for a shared haplotype in this region, which delineated a critical interval of 3.35 Mb. We sequenced the genome of an affected Eurasier and compared it with the Boxer reference genome and 47 control genomes of dogs from other breeds. This analysis revealed 4 private non-synonymous variants in the critical interval of the affected Eurasier. We genotyped these variants in additional dogs and found perfect association for only one of these variants, a single base deletion in the VLDLR gene encoding the very low density lipoprotein receptor. This variant, VLDLR:c.1713delC is predicted to cause a frameshift and premature stop codon (p.W572Gfs*10). Variants in the VLDLR gene have been shown to cause congenital cerebellar ataxia and mental retardation in human patients and Vldlr knockout mice also display an ataxia phenotype. Our combined genetic data together with the functional knowledge on the VLDLR gene from other species thus strongly suggest that VLDLR:c.1713delC is indeed causing DWLM in Eurasier dogs.http://europepmc.org/articles/PMC4323105?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Martina Gerber
Andrea Fischer
Vidhya Jagannathan
Michaela Drögemüller
Cord Drögemüller
Martin J Schmidt
Filipa Bernardino
Eberhard Manz
Kaspar Matiasek
Kai Rentmeister
Tosso Leeb
spellingShingle Martina Gerber
Andrea Fischer
Vidhya Jagannathan
Michaela Drögemüller
Cord Drögemüller
Martin J Schmidt
Filipa Bernardino
Eberhard Manz
Kaspar Matiasek
Kai Rentmeister
Tosso Leeb
A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).
PLoS ONE
author_facet Martina Gerber
Andrea Fischer
Vidhya Jagannathan
Michaela Drögemüller
Cord Drögemüller
Martin J Schmidt
Filipa Bernardino
Eberhard Manz
Kaspar Matiasek
Kai Rentmeister
Tosso Leeb
author_sort Martina Gerber
title A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).
title_short A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).
title_full A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).
title_fullStr A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).
title_full_unstemmed A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).
title_sort deletion in the vldlr gene in eurasier dogs with cerebellar hypoplasia resembling a dandy-walker-like malformation (dwlm).
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Dandy-Walker-like malformation (DWLM) is the result of aberrant brain development and mainly characterized by cerebellar hypoplasia. DWLM affected dogs display a non-progressive cerebellar ataxia. Several DWLM cases were recently observed in the Eurasier dog breed, which strongly suggested a monogenic autosomal recessive inheritance in this breed. We performed a genome-wide association study (GWAS) with 9 cases and 11 controls and found the best association of DWLM with markers on chromosome 1. Subsequent homozygosity mapping confirmed that all 9 cases were homozygous for a shared haplotype in this region, which delineated a critical interval of 3.35 Mb. We sequenced the genome of an affected Eurasier and compared it with the Boxer reference genome and 47 control genomes of dogs from other breeds. This analysis revealed 4 private non-synonymous variants in the critical interval of the affected Eurasier. We genotyped these variants in additional dogs and found perfect association for only one of these variants, a single base deletion in the VLDLR gene encoding the very low density lipoprotein receptor. This variant, VLDLR:c.1713delC is predicted to cause a frameshift and premature stop codon (p.W572Gfs*10). Variants in the VLDLR gene have been shown to cause congenital cerebellar ataxia and mental retardation in human patients and Vldlr knockout mice also display an ataxia phenotype. Our combined genetic data together with the functional knowledge on the VLDLR gene from other species thus strongly suggest that VLDLR:c.1713delC is indeed causing DWLM in Eurasier dogs.
url http://europepmc.org/articles/PMC4323105?pdf=render
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