A missense mutation in the gene for melanocyte-stimulating hormone receptor (MCIR) is associated with the chestnut coat color in horses

Abstract

The melanocyte-stimulating hormone receptor gene (MCIR) is the major candidate gene for the chestnut coat color in horses since it is assumed to be controlled by an allele at the extension locus. MCIR sequences were PCR amplified from chestnut (e/e) and non-chestnut (EI-) horses. A single-strand conformation polymorphism was found that showed a complete association to the chestnut coat color among 144 horses representing 12 breeds. Sequence analysis revealed a single missense mutation (83Ser → Phe) in the MCIR allele associated with the chestnut color. The substitution occurs in the second transmembrane region, which apparently plays a key role in the molecule since substitutions associated with coat color variants in mice and cattle as well as red hair and fair skin in humans are found in this part of the molecule. We propose that the now reported mutation is likely to be the causative mutation for the chestnut coat color. The polymorphism can be detected with a simple PCR-RFLP test, since the mutation creates a TaqI restriction site in the chestnut allele.

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Correspondence to L. Marklund or M. Johansson Moller or K. Sandberg or L. Andersson.

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The nucleotide sequence data reported in this paper have been submitted to GenBank and have been assigned the accession number X98012.

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Marklund, L., Moller, M.J., Sandberg, K. et al. A missense mutation in the gene for melanocyte-stimulating hormone receptor (MCIR) is associated with the chestnut coat color in horses. Mammalian Genome 7, 895–899 (1996). https://doi.org/10.1007/s003359900264

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Keywords

  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Coat Color
  • Chestnut Horse
  • Fair Skin
  • Icelandic Horse