Genome-Wide Association Study of Golden Retrievers Identifies Germ-Line Risk Factors Predisposing to Mast Cell Tumours

被引:41
作者
Arendt, Maja L. [1 ,2 ]
Melin, Malin [1 ]
Tonomura, Noriko [3 ,4 ]
Koltookian, Michele [3 ]
Courtay-Cahen, Celine [5 ]
Flindall, Netty [5 ]
Bass, Joyce [5 ]
Boerkamp, Kim [6 ]
Megquir, Katherine [1 ,3 ,4 ]
Youell, Lisa [5 ]
Murphy, Sue [5 ]
McCarthy, Colleen [3 ]
London, Cheryl [7 ]
Rutteman, Gerard R. [6 ,8 ]
Starkey, Mike [5 ]
Lindblad-Toh, Kerstin [1 ,3 ]
机构
[1] Uppsala Univ, Dept Med Biochem & Microbiol, Sci Life Lab, Uppsala, Sweden
[2] Univ Cambridge, Dept Vet Med, Cambridge, England
[3] Broad Inst MIT & Harvard, Cambridge, MA USA
[4] Tufts Univ, Cummings Sch Vet Med, Dept Clin Sci, North Grafton, MA USA
[5] Anim Hlth Trust, Newmarket, Suffolk, England
[6] Univ Utrecht, Dept Clin Sci Compan Anim, Utrecht, Netherlands
[7] Ohio State Univ, Dept Vet Clin Sci, Columbus, OH 43210 USA
[8] Vet Specialist Ctr De Wagenrenk, Wageningen, Netherlands
基金
瑞典研究理事会;
关键词
C-KIT; SYSTEMIC MASTOCYTOSIS; HYALURONIC-ACID; MUTATIONS; DOGS; RAT; FIBROBLASTS; SEQUENCE; SURVIVAL; EXPRESS;
D O I
10.1371/journal.pgen.1005647
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Canine mast cell tumours (CMCT) are one of the most common skin tumours in dogs with a major impact on canine health. Certain breeds have a higher risk of developing mast cell tumours, suggesting that underlying predisposing germ-line genetic factors play a role in the development of this disease. The genetic risk factors are largely unknown, although somatic mutations in the oncogene C-KIT have been detected in a proportion of CMCT, making CMCT a comparative model for mastocytosis in humans where C-KIT mutations are frequent. We have performed a genome wide association study in golden retrievers from two continents and identified separate regions in the genome associated with risk of CMCT in the two populations. Sequence capture of associated regions and subsequent fine mapping in a larger cohort of dogs identified a SNP associated with development of CMCT in the GNAI2 gene (p = 2.2x10(-16)), introducing an alternative splice form of this gene resulting in a truncated protein. In addition, disease associated haplotypes harbouring the hyaluronidase genes HYAL1, HYAL2 and HYAL3 on cfa20 and HYAL4, SPAM1 and HYALP1 on cfa14 were identified as separate risk factors in European and US golden retrievers, respectively, suggesting that turnover of hyaluronan plays an important role in the development of CMCT.
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页数:21
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