Wolber Lisa E, Girotto Giorgia, Buniello Annalisa, Vuckovic Dragana, Pirastu Nicola, Lorente-Cánovas Beatriz, Rudan Igor, Hayward Caroline, Polasek Ozren, Ciullo Marina, Mangino Massimo, Steves Claire, Concas Maria Pina, Cocca Massilimiliano, Spector Tim D, Gasparini Paolo, Steel Karen P, Williams Frances M K
Department of Twin Research and Genetic Epidemiology, King's College London, London SE1 7EH, UK.
Medical Genetics, Department of Reproductive Sciences, Development and Public Health, IRCCS-Burlo Garofolo Children Hospital, University of Trieste, Trieste 34100, Italy.
Hum Mol Genet. 2014 Dec 1;23(23):6407-18. doi: 10.1093/hmg/ddu346. Epub 2014 Jul 24.
Hearing function is known to be heritable, but few significant and reproducible associations of genetic variants have been identified to date in the adult population. In this study, genome-wide association results of hearing function from the G-EAR consortium and TwinsUK were used for meta-analysis. Hearing ability in eight population samples of Northern and Southern European ancestry (n = 4591) and the Silk Road (n = 348) was measured using pure-tone audiometry and summarized using principal component (PC) analysis. Genome-wide association analyses for PC1-3 were conducted separately in each sample assuming an additive model adjusted for age, sex and relatedness of subjects. Meta-analysis was performed using 2.3 million single-nucleotide polymorphisms (SNPs) tested against each of the three PCs of hearing ability in 4939 individuals. A single SNP lying in intron 6 of the salt-inducible kinase 3 (SIK3) gene was found to be associated with hearing PC2 (P = 3.7×10(-8)) and further supported by whole-genome sequence in a subset. To determine the relevance of this gene in the ear, expression of the Sik3 protein was studied in mouse cochlea of different ages. Sik3 was expressed in murine hair cells during early development and in cells of the spiral ganglion during early development and adulthood. Our results suggest a developmental role of Sik3 in hearing and may be required for the maintenance of adult auditory function.
已知听力功能具有遗传性,但迄今为止,在成年人群中尚未发现有显著且可重复的基因变异关联。在本研究中,来自G-EAR联盟和TwinsUK的听力功能全基因组关联结果被用于荟萃分析。使用纯音听力测定法测量了北欧和南欧血统的八个群体样本(n = 4591)以及丝绸之路群体样本(n = 348)的听力能力,并通过主成分(PC)分析进行总结。在每个样本中分别针对PC1-3进行全基因组关联分析,假设采用针对年龄、性别和受试者亲缘关系进行调整的加性模型。使用230万个单核苷酸多态性(SNP)对4939名个体的听力能力的三个PC中的每一个进行测试,进行荟萃分析。发现位于盐诱导激酶3(SIK3)基因内含子6中的一个SNP与听力PC2相关(P = 3.7×10^(-8)),并且在一个子集中得到了全基因组序列的进一步支持。为了确定该基因在耳朵中的相关性,研究了不同年龄小鼠耳蜗中Sik3蛋白的表达。Sik3在早期发育阶段在小鼠毛细胞中表达,在早期发育阶段和成年期在螺旋神经节细胞中表达。我们的结果表明Sik3在听力发育中起作用,并且可能是维持成人听觉功能所必需的。