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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)
- 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.
- Subjects :
- Coat
lcsh:QH426-470
[SDV]Life Sciences [q-bio]
Locus (genetics)
Biology
oryctolagus cuniculus
03 medical and health sciences
Black hair
COAT COLOUR
BREEDS
RABBIT
Genotype
MC1R
Genetics
Animals
Genetics(clinical)
melanocortin
Allele
Hair Color
gene
Genetics (clinical)
030304 developmental biology
Dominance (genetics)
Sequence Deletion
0303 health sciences
rabbit
mc1r
coat
Base Sequence
MUTATIONS
0402 animal and dairy science
Wild type
04 agricultural and veterinary sciences
040201 dairy & animal science
Molecular biology
lcsh:Genetics
Agouti Signaling Protein
Rabbits
Receptor, Melanocortin, Type 1
Melanocortin 1 receptor
Research Article
Subjects
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⟩