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A composite six bp in-frame deletion in the melanocortin 1 receptor (MC1R) gene is associated with the japanese brindling coat colour in rabbits (Oryctolagus Cuniculus)

Authors :
Michela Colombo
Ahmad Oulmouden
Stefania Dall'Olio
Emilio Scotti
Daniel Allain
Luca Fontanesi
Francesca Beretti
Séverine Deretz
Vincenzo Russo
Lionel Forestier
Fontanesi, Luca
Fontanesi L.
Scotti E.
Colombo M.
Beretti F.
Forestier L.
Dall'Olio S.
Deretz S.
Russo V.
Allain D.
Oulmouden A.
DIPROVAL
Alma Mater Studiorum University of Bologna (UNIBO)
Unité de Génétique Moléculaire Animale (UMR GMA)
Institut National de la Recherche Agronomique (INRA)-Université de Limoges (UNILIM)
Génétique Expérimentale en Productions Animales (GEPA)
Institut National de la Recherche Agronomique (INRA)
Station d'Amélioration Génétique des Animaux (SAGA)
Unité de Génétique Moléculaire Animale (UGMA)
Université de Limoges (UNILIM)-Institut National de la Recherche Agronomique (INRA)
Source :
BMC Genetics july (11, online), Non paginé. (2010), BMC Genetics, Vol 11, Iss 1, p 59 (2010), BMC Genetics, BMC Genetics, BioMed Central, 2010, 11, online (july), Non paginé. ⟨10.1186/1471-2156-11-59⟩
Publication Year :
2010

Abstract

Background In the domestic rabbit (Oryctolagus cuniculus), classical genetic studies have identified five alleles at the Extension locus: ED (dominant black), ES (steel, weaker version of ED), E (wild type, normal extension of black), eJ(Japanese brindling, mosaic distribution of black and yellow) and e (non-extension of black, yellow/red with white belly). Sequencing almost the complete coding sequence (CDS) of the rabbit MC1R gene, we recently identified two in-frame deletions associated with dominant black (c.280_285del6; alleles ED or ES) and recessive red (c.304_333del30; allele e) coat colours. It remained to characterize the eJallele whose phenotypic effect is similar to the Orange and Sex-linked yellow loci of cat and Syrian hamster. Results We sequenced the whole CDS in 25 rabbits of different coat colours including 10 Japanese and 10 Rhinelander (tricolour) rabbits and identified another 6 bp-in frame deletion flanked by a G > A transition in 5' (c.[124G>A;125_130del6]) that was present in all animals with Japanese brindling coat colour and pattern. These mutations eliminate two amino acids in the first transmembrane domain and, in addition, cause an amino acid substitution at position 44 of the wild type sequence. Genotyping 371 rabbits of 31 breeds with different coat colour this allele (eJ) was present in homozygous state in Japanese, Rhinelander and Dutch tricolour rabbits only (except one albino rabbit). Rabbits with eJ/eJ genotype were non fixed at the non-agouti mutation we previously identified in the ASIP gene. Segregation in F1 and F2 families confirmed the order of dominance already determined by classical genetic experiments with a possible dose effect evident comparing eJ/eJ and eJ/e animals. MC1R mRNA was expressed in black hair skin regions only. Conclusions The c.[124A;125_130del6] allele may be responsible for a MC1R variant determining eumelanin production in the black areas. However, the mechanism determining the presence of both red and black hairs in the same animal seems more complex. Expression analyses of the c.[124A;125_130del6] allele suggest that MC1R transcription may be regulated epigenetically in rabbits with the Japanese brindling phenotype. Further studies are needed to clarify this issue.

Details

Language :
English
ISSN :
14712156
Database :
OpenAIRE
Journal :
BMC Genetics july (11, online), Non paginé. (2010), BMC Genetics, Vol 11, Iss 1, p 59 (2010), BMC Genetics, BMC Genetics, BioMed Central, 2010, 11, online (july), Non paginé. ⟨10.1186/1471-2156-11-59⟩
Accession number :
edsair.doi.dedup.....e6440620646370cc83ac6ae76b57cc01
Full Text :
https://doi.org/10.1186/1471-2156-11-59⟩