5′UTR Variant in KIT Associated With White Spotting in Horses

被引:3
|
作者
McFadden, Aiden [1 ]
Martin, Katie [1 ]
Foster, Gabriel [1 ]
Vierra, Micaela [1 ]
Lundquist, Erica W. [1 ]
Everts, Robin E. [1 ]
Martin, Erik [1 ]
Volz, Erin [1 ]
McLoone, Kaitlyn [1 ]
Brooks, Samantha A. [2 ]
Lafayette, Christa [1 ]
机构
[1] Etalon Inc, Menlo Pk, CA 94025 USA
[2] UF Genet Inst Univ Florida, Dept Anim Sci, Gainesville, FL USA
关键词
Horse; KIT; Mutation; Depigmentation; Genetics; GENE; MUTATIONS; PATTERN; LIGAND;
D O I
10.1016/j.jevs.2023.104563
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Mutations in KIT, a gene that influences melanoblast migration and pigmentation, often result in mammalian white spotting. As of February 2023, over 30 KIT variants associated with white spotting were documented in Equus caballus (horse). Here we report an association of increased white spotting on the skin and coat with a variant in the 5'UTR of KIT (rs1149701677: g.79,618,649A>C). Horses possessing at least one alternate allele demonstrate phenotypic characteristics similar to other KIT mutations: clear borders around unpigmented regions on the body, face, and limbs. Using a quantitative measure of depigmentation, we observed an average white score of 10.70 among individuals with rs1149701677, while the average score of the control, homozygous reference sample was 2.23 (P = 1.892e-11, n = 109, t-test). The rs1149701677 site has a cross-species conservation score of 3.4, one of the highest scores across the KIT 5'UTR, implying regulatory importance for this site. Ensembl also predicted a "moderately impactful" functional effect for the rs1149701677 variant. We propose that this single nucleotide variant likely alters the regulation of KIT, which in turn may disrupt melanoblast migration causing an increase in white spotting on the coat. Alternatively, the rs1149701677 variant may be in linkage with another nearby variant with an as-yet-undiscovered functional impact. We propose to term this new allele "Holiday White" or W35 based on conventional nomenclature. (c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页数:4
相关论文
共 50 条
  • [21] Mutations in MITF and PAX3 Cause "Splashed White" and Other White Spotting Phenotypes in Horses
    Hauswirth, Regula
    Haase, Bianca
    Blatter, Marlis
    Brooks, Samantha A.
    Burger, Dominik
    Droegemueller, Cord
    Gerber, Vincent
    Henke, Diana
    Janda, Jozef
    Jude, Rony
    Magdesian, K. Gary
    Matthews, Jacqueline M.
    Poncet, Pierre-Andre
    Svansson, Vilhjalmur
    Tozaki, Teruaki
    Wilkinson-White, Lorna
    Penedo, M. Cecilia T.
    Rieder, Stefan
    Leeb, Tosso
    PLOS GENETICS, 2012, 8 (04): : 404 - 412
  • [22] A de novo mutation in KIT causes white spotting in a subpopulation of German Shepherd dogs
    Wong, A. K.
    Ruhe, A. L.
    Robertson, K. R.
    Loew, E. R.
    Williams, D. C.
    Neff, M. W.
    ANIMAL GENETICS, 2013, 44 (03) : 305 - 310
  • [23] Genomic analysis reveals the association of KIT and MITF variants with the white spotting in swamp buffaloes
    Dai, Dongmei
    Sari, Eka Meutia
    Si, Jingfang
    Ashari, Hidayat
    Dagong, Muhammad Ihsan Andi
    Pauciullo, Alfredo
    Lenstra, Johannes A.
    Han, Jianlin
    Zhang, Yi
    BMC GENOMICS, 2024, 25 (01):
  • [24] Allelic heterogeneity at the equine KIT locus in dominant white (W) horses
    Haase, Bianca
    Brooks, Samantha A.
    Schlumbaum, Angela
    Azor, Pedro J.
    Bailey, Ernest
    Alaeddine, Ferial
    Mevissen, Meike
    Burger, Dominik
    Poncet, Pierre-Andre
    Rieder, Stefan
    Leeb, Tosso
    PLOS GENETICS, 2007, 3 (11): : 2101 - 2108
  • [25] Seven novel KIT mutations in horses with white coat colour phenotypes
    Haase, B.
    Brooks, S. A.
    Tozaki, T.
    Burger, D.
    Poncet, P. -A.
    Rieder, S.
    Hasegawa, T.
    Penedo, C.
    Leeb, T.
    ANIMAL GENETICS, 2009, 40 (05) : 623 - 629
  • [26] Five novel KIT mutations in horses with white coat colour phenotypes
    Haase, B.
    Rieder, S.
    Tozaki, T.
    Hasegawa, T.
    Penedo, M. C. T.
    Jude, R.
    Leeb, T.
    ANIMAL GENETICS, 2011, 42 (03) : 337 - 339
  • [27] A Variant in a MicroRNA complementary site in the 3′ UTR of the KIT oncogene increases risk of acral melanoma
    Godshalk, S. E.
    Paranjape, T.
    Nallur, S.
    Speed, W.
    Chan, E.
    Molinaro, A. M.
    Bacchiocchi, A.
    Hoyt, K.
    Tworkoski, K.
    Stern, D. F.
    Sznol, M.
    Ariyan, S.
    Lazova, R.
    Halaban, R.
    Kidd, K. K.
    Weidhaas, J. B.
    Slack, F. J.
    ONCOGENE, 2011, 30 (13) : 1542 - 1550
  • [28] A Variant in a MicroRNA complementary site in the 3′ UTR of the KIT oncogene increases risk of acral melanoma
    S E Godshalk
    T Paranjape
    S Nallur
    W Speed
    E Chan
    A M Molinaro
    A Bacchiocchi
    K Hoyt
    K Tworkoski
    D F Stern
    M Sznol
    S Ariyan
    R Lazova
    R Halaban
    K K Kidd
    J B Weidhaas
    F J Slack
    Oncogene, 2011, 30 : 1542 - 1550
  • [29] White spotting variant mouse as an experimental model for ovarian aging and menopausal biology
    Smith, Elizabeth R.
    Yeasky, Toni
    Wei, Jain Qin
    Miki, Roberto A.
    Cai, Kathy Q.
    Smedberg, Jennifer L.
    Yang, Wan-Lin
    Xu, Xiang-Xi
    MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY, 2012, 19 (05): : 588 - 596
  • [30] Functional analysis of a CDKN2A 5'UTR germline variant associated with pancreatic cancer development
    Bruno, William
    Andreotti, Virginia
    Bisio, Alessandra
    Pastorino, Lorenza
    Fornarini, Giuseppe
    Sciallero, Stefania
    Bianchi-Scarra, Giovanna
    Inga, Alberto
    Ghiorzo, Paola
    PLOS ONE, 2017, 12 (12):