Variation in Genes Related to Cochlear Biology Is Strongly Associated with Adult-Onset Deafness in Border Collies
Domestic dogs can suffer from hearing losses that can have profound impacts on working ability and quality of life. We have identified a type of adult-onset hearing loss in Border Collies that appears to have a genetic cause, with an earlier age of onset (3–5 years) than typically expected for aging dogs (8–10 years). Studying this complex trait within pure breeds of dog may greatly increase our ability to identify genomic regions associated with risk of hearing impairment in dogs and in humans. We performed a genome-wide association study (GWAS) to detect loci underlying adult-onset deafness in a sample of 20 affected and 28 control Border Collies. We identified a region on canine chromosome 6 that demonstrates extended support for association surrounding SNP Chr6.25819273 (p-value = 1.09×10−13). To further localize disease-associated variants, targeted next-generation sequencing (NGS) of one affected and two unaffected dogs was performed. Through additional validation based on targeted genotyping of additional cases (n = 23 total) and controls (n = 101 total) and an independent replication cohort of 16 cases and 265 controls, we identified variants in USP31 that were strongly associated with adult-onset deafness in Border Collies, suggesting the involvement of the NF-κB pathway. We found additional support for involvement of RBBP6, which is critical for cochlear development. These findings highlight the utility of GWAS–guided fine-mapping of genetic loci using targeted NGS to study hereditary disorders of the domestic dog that may be analogous to human disorders.
Vyšlo v časopise:
Variation in Genes Related to Cochlear Biology Is Strongly Associated with Adult-Onset Deafness in Border Collies. PLoS Genet 8(9): e32767. doi:10.1371/journal.pgen.1002898
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1002898
Souhrn
Domestic dogs can suffer from hearing losses that can have profound impacts on working ability and quality of life. We have identified a type of adult-onset hearing loss in Border Collies that appears to have a genetic cause, with an earlier age of onset (3–5 years) than typically expected for aging dogs (8–10 years). Studying this complex trait within pure breeds of dog may greatly increase our ability to identify genomic regions associated with risk of hearing impairment in dogs and in humans. We performed a genome-wide association study (GWAS) to detect loci underlying adult-onset deafness in a sample of 20 affected and 28 control Border Collies. We identified a region on canine chromosome 6 that demonstrates extended support for association surrounding SNP Chr6.25819273 (p-value = 1.09×10−13). To further localize disease-associated variants, targeted next-generation sequencing (NGS) of one affected and two unaffected dogs was performed. Through additional validation based on targeted genotyping of additional cases (n = 23 total) and controls (n = 101 total) and an independent replication cohort of 16 cases and 265 controls, we identified variants in USP31 that were strongly associated with adult-onset deafness in Border Collies, suggesting the involvement of the NF-κB pathway. We found additional support for involvement of RBBP6, which is critical for cochlear development. These findings highlight the utility of GWAS–guided fine-mapping of genetic loci using targeted NGS to study hereditary disorders of the domestic dog that may be analogous to human disorders.
Zdroje
1. GatesGA, MillsJH (2005) Presbycusis. Lancet 366: 1111–1120 S0140-6736(05)67423-5 [pii];10.1016/S0140-6736(05)67423-5 [doi].
2. KarlssonKK, HarrisJR, SvartengrenM (1997) Description and primary results from an audiometric study of male twins. Ear Hear 18: 114–120.
3. LiuXZ, YanD (2007) Ageing and hearing loss. J Pathol 211: 188–197.
4. BaiU, SeidmanMD, HinojosaR, QuirkWS (1997) Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study. Am J Otol 18: 449–453.
5. Fischel-GhodsianN, BykhovskayaY, TaylorK, KahenT, CantorR, et al. (1997) Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations. Hear Res 110: 147–154 S0378-5955(97)00077-4 [pii].
6. Van LaerL, HuygheJR, HannulaS, Van EykenE, StephanDA, et al. (2010) A genome-wide association study for age-related hearing impairment in the Saami. Eur J Hum Genet In press.
7. FriedmanRA, Van LaerL, HuentelmanMJ, ShethSS, Van EykenE, et al. (2009) GRM7 variants confer susceptibility to age-related hearing impairment. Human Molecular Genetics 18: 785–796.
8. TerHG, Venker-van HaagenAJ, van den BromWE, van SluijsFJ, SmoorenburgGF (2008) Effects of aging on brainstem responses to toneburst auditory stimuli: a cross-sectional and longitudinal study in dogs. J Vet Intern Med 22: 937–945.
9. KnowlesK, BlauchB, LeipoldH, CashW, HewettJ (1989) Reduction of spiral ganglion neurons in the aging canine with hearing loss. Zentralbl Veterinarmed A 36: 188–199.
10. ShimadaA, EbisuM, MoritaT, TakeuchiT, UmemuraT (1998) Age-Related Changes in the Cochlea and Cochlear Nuclei of Dogs. The Journal of Veterinary Medical Science 60: 41–48.
11. SchuknechtHF, GacekMR (1993) Cochlear pathology in presbycusis. Ann Otol Rhinol Laryngol 102: 1–16.
12. TerHG, de GrootJC, Venker-van HaagenAJ, van SluijsFJ, SmoorenburgGF (2009) Effects of aging on inner ear morphology in dogs in relation to brainstem responses to toneburst auditory stimuli. J Vet Intern Med 23: 536–543.
13. United States Border Collie Handlers' Association 2011 Sheep Dog Pedigrees. Available: www.usbcha.com/events/sheep/pedigrees.html. Accessed 2012 May 23.
14. StrainGM (1996) Aetiology, prevalence and diagnosis of deafness in dogs and cats. Br Vet J 152: 17–36.
15. ShworakNW, LiuJ, PetrosLM, ZhangL, KobayashiM, et al. (1999) Multiple isoforms of heparan sulfate D-glucosaminyl 3-O-sulfotransferase. Isolation, characterization, and expression of human cdnas and identification of distinct genomic loci. J Biol Chem 274: 5170–5184.
16. ZwaenepoelI, MustaphaM, LeiboviciM, VerpyE, GoodyearR, et al. (2002) Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. Proceedings of the National Academy of Sciences of the United States of America 99: 6240–6245.
17. RoweTM, RizziM, HiroseK, PetersGA, SenGC (2006) A role of the double-stranded RNA-binding protein PACT in mouse ear development and hearing. Proc Natl Acad Sci U S A 103: 5823–5828 0601287103 [pii];10.1073/pnas.0601287103 [doi].
18. LockhartPJ, HulihanM, LincolnS, HusseyJ, SkipperL, et al. (2004) Identification of the human ubiquitin specific protease 31 (USP31) gene: structure, sequence and expression analysis. DNA Seq 15: 9–14.
19. LangH, SchulteBA, ZhouD, SmytheN, SpicerSS, et al. (2006) Nuclear factor kappaB deficiency is associated with auditory nerve degeneration and increased noise-induced hearing loss. J Neurosci 26: 3541–3550 26/13/3541 [pii];10.1523/JNEUROSCI.2488-05.2006 [doi].
20. TzimasC, MichailidouG, ArsenakisM, KieffE, MosialosG, et al. (2006) Human ubiquitin specific protease 31 is a deubiquitinating enzyme implicated in activation of nuclear factor-kappaB. Cell Signal 18: 83–92 S0898-6568(05)00074-4 [pii];10.1016/j.cellsig.2005.03.017 [doi].
21. KappoMA, EisoAB, HassemF, AtkinsonRA, FaroA, et al. (2012) Solution Structure of RING Finger-like Domain of Retinoblastoma-binding Protein-6 (RBBP6) Suggests It Functions as a U-box. J Biol Chem 287 (10) 7146–58.
22. AlvarezCE, AkeyJM (2012) Copy number variation in the domestic dog. Mamm Genome 23: 144–163 10.1007/s00335-011-9369-8 [doi].
23. PurcellS, NealeB, Todd-BrownK, ThomasL, FerreiraMA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559–575.
24. KangHM, SulJH, ServiceSK, ZaitlenNA, KongSy, et al. (2010) Variance component model to account for sample structure in genome-wide association studies. Nat Genet 42: 348–354.
25. LangmeadB, TrapnellC, PopM, SalzbergSL (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 10: R25 gb-2009-10-3-r25 [pii];10.1186/gb-2009-10-3-r25 [doi].
26. LiH, HandsakerB, WysokerA, FennellT, RuanJ, et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics 25: 2078–2079 btp352 [pii];10.1093/bioinformatics/btp352 [doi].
27. QuinlanAR, HallIM (2010) BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics 26: 841–842 btq033 [pii];10.1093/bioinformatics/btq033 [doi].
28. McKennaA, HannaM, BanksE, SivachenkoA, CibulskisK, et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20: 1297–1303 gr.107524.110 [pii];10.1101/gr.107524.110 [doi].
29. AlbersCA, LunterG, MacArthurDG, McVeanG, OuwehandWH, et al. (2011) Dindel: accurate indel calls from short-read data. Genome Res 21: 961–973 gr.112326.110 [pii];10.1101/gr.112326.110 [doi].
30. WangK, LiM, HakonarsonH (2010) ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucl Acids Res 38: e164.
31. KentWJ, SugnetCW, FureyTS, RoskinKM, PringleTH, et al. (2002) The Human Genome Browser at UCSC. Genome Res 12: 996–1006.
32. WillerCJ, LiY, AbecasisGR (2010) METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26: 2190–2191 btq340 [pii];10.1093/bioinformatics/btq340 [doi].
33. ChenZQ, AnniloT, ShuleninS, DeanM (2004) Three ATP-binding cassette transporter genes, Abca14, Abca15, and Abca16, form a cluster on mouse chromosome 7F3. Mamm Genome 15: 335–43.
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2012 Číslo 9
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