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Journal of Heredity Advance Access first published online on May 22, 2007
This version published online on June 27, 2007

Journal of Heredity, doi:10.1093/jhered/esm021
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© The American Genetic Association. 2007. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org.

A Noncoding Melanophilin Gene (MLPH) SNP at the Splice Donor of Exon 1 Represents a Candidate Causal Mutation for Coat Color Dilution in Dogs

Cord Drögemüller*, Ute Philipp*, Bianca Haase, Anne-Rose Günzel-apel, and Tosso Leeb

From the Institute of Genetics, Vetsuisse Faculty, University of Berne, Bremgartenstrasse 109a, 3001 Berne, Switzerland (Drögemüller, Haase, Leeb); the Institute of Animal Breeding and Genetics, University of Veterinary Medicine Hannover, Bünteweg 17p, 30559 Hannover, Germany (Philipp); and the Small Animal Clinic—Unit for Reproductive Medicine, University of Veterinary Medicine Hannover, Bünteweg 15, 30559 Hannover, Germany (Günzel-Apel)

Address correspondence to: Dr. T. Leeb at the address above, or e-mail: tosso.leeb{at}itz.unibe.ch.

Coat color dilution in several breeds of dog is characterized by a specific pigmentation phenotype and sometimes accompanied by hair loss and recurrent skin inflammation, the so-called color dilution alopecia or black hair follicular dysplasia. Coat color dilution (d) is inherited as a Mendelian autosomal recessive trait. In a previous study, MLPH polymorphisms showed perfect cosegregation with the dilute phenotype within breeds. However, different dilute haplotypes were found in different breeds, and no single polymorphism was identified in the coding sequence that was likely to be causative for the dilute phenotype. We resequenced the 5'-region of the canine MLPH gene and identified a strong candidate single nucleotide polymorphism within the nontranslated exon 1, which showed perfect association to the dilute phenotype in 65 dilute dogs from 7 different breeds. The A/G polymorphism is located at the last nucleotide of exon 1 and the mutant A-allele is predicted to reduce splicing efficiency 8-fold. An MLPH mRNA expression study using quantitative reverse transcriptase–polymerase chain reaction confirmed that dd animals had only about approximately 25% of the MLPH transcript compared with DD animals. These results provide preliminary evidence that the reported regulatory MLPH mutation might represent a causal mutation for coat color dilution in dogs.


* These authors contributed equally to the work.

Corresponding Editor: Steven Hannah

The symposium paragraph for this article has been inserted.


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