A genetic variant determines speed of hair greying and susceptibility to skin melanoma in horses
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A genetic variant determines speed of hair greying and susceptibility to skin melanoma in horses

04/09/2024 Uppsala Universitet

Greying with age is a common coat colour variant in horses, characterized by progressive hair greying and susceptibility to skin melanoma. In a new study published in Nature Communications, an international consortium led by scientists from Uppsala University (Sweden) now reports that the speed of greying and susceptibility to melanoma are determined by the copy number of a small duplicated DNA sequence in the gene Syntaxin 17.

Grey horses are born normally coloured but already during their first year of life a hair greying process is initiated that usually results in them becoming completely white later in life, one of the most iconic coat colour variants in animals. At an older age, white horses carrying the Grey mutation often develop skin melanomas that are usually benign but some develop into a malignant form. These horses have white hair but completely black skin and do not get melanoma because they are sensitive to UV damage, a major riskfactor for human melanoma, but due to an intrinsic effect of the Grey mutation.

“In a previous study, we reported that Greying with age is associated with a duplication of a small piece (4,600 base pairs) in an intron of the gene that codes for the protein Syntaxin 17”, explains professor Leif Andersson (Uppsala University). “We also showed that the duplicated sequence constitutes an enhancer that upregulates expression of Syntaxin 17 as well as the neighbouring gene NR4A3”. (An enhancer is a peice of DNA that do not code for any protein but takes part in the regulation of gene expression).

“In this new study we show that there are three different gene variants at the Grey locus in horse, G1 with no duplication (wild type), G2 with two copies of the duplicated sequence causing slow greying and no detected higher risk of melanoma and G3 with three copies of the duplicated sequence and a significantly elevated risk of skin melanoma” explains Dr. Carl-Johan Rubin (Uppsala University) first author on the study.

Since a horse have two copies of each chromosome, a horse can have two, three, four, five and six copies of the duplicated sequence depending on its genotype at the Grey locus.
“We find a remarkable dosage effect where the speed of greying and melanoma susceptibility increase as a function of the copy number of the duplicated sequence”, continues Leif Andersson. “There appears to be a treshold effect so that the G3 variant with three copies is needed in order to see an increased risk of melanoma”.

The discovery reported in this study is based on the association between slow greying and the G2 gene variant in two different breeds, Swedish Connemara ponies and Japanese Thoroughbred horses.
“The discovery that G2 arose by mutation from a G3 variant in our Japanese pedigree provides the ultimate evidence that the duplication is causing hair greying”, explains one of the coauthors Teruaki Tozaki (Laboratory of Racing Chemistry, Tochigi, Japan). “The G3 variant simply lost one of the copies when the gamete was formed, illustrating genetic instability when a sequence occurs in multiple copies on a chromosome”.

In this study the authors genotyped 1,400 horses representing 78 breeds. They found the G3 variant associated with fast greying and white colour in 62 breeds while the G2 allele associated with slow greying and grey colour was only found in eigth breeds.
“It is likely that there has been a strong selection for the G3 variant because of the preference for the beauty of white horses, says Prof. Rebecca Bellone at Veterinary Genetics Laboratory (UC Davis) responsible for the genotyping of the 1,400 horses. “Now we have a genetic test to offer that can tell at an early age whether a horse will be grey or white later in life, and whether it has an elevated risk of skin melanoma.”

“The remaining mystery we hope to solve in future research is why an elevated expression of the Syntaxin 17 and/or NR4A3 genes result in progressive hair greying and susceptibility to melanoma”, ends Leif Andersson. “If we can solve this enigma it has implications for understanding tumour development in general, and may have important implications for prevention and/or treatment of melanomas in these horses.
Rubin C-J et al. (2024) An intronic copy number variation in Syntaxin 17 determines speed of greying and melanoma incidence in Grey horses. Nature Communications. 15:7510. https://doi.org/10.1038/s41467-024-51898-2.
Attached files
  • Schematic description of the mutation causing hair greying and susceptibility to melanoma in horses. The mutation causing Greying with age is a copy number variation of a 4,600 bp long sequence located in intron 6 of the Syntaxin 17 gene. The duplicated sequence harbours binding sites for the protein MITF which regulates gene expression in pigment cells. The presence of the duplicated sequence upregulates the expression of both Syntaxin 17 and the neighbouring gene NR4A3. G1 has a single copy of the 4,600 base pair sequence and is associated with normal coat colour, G2 carries two copies and causes slow greying, and G3 carries three copies and causes fast greying.
  • Comparison of fast grey and slow grey coat colour in Connemara ponies. Left: Fast greying Connemara stallion at 15 years of age. Photographer: Linda Lindblad. Right: Slow greying Connemara stallion at 23 years. Photographer: Marlene Näslin.
  • Six shades of grey. Three fast greying Connemara dams with their progenies sired by a slow greying stallion. Time or a DNA test will tell if the foals will be fast or slow greying. Photographer: Maria Johansson.
04/09/2024 Uppsala Universitet
Regions: Europe, Sweden, Asia, Japan
Keywords: Science, Life Sciences

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