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Gene-gene interaction between RBMS3 and ZNF516 influences bone mineral density

机译:RBMS3和ZNF516之间的基因-基因相互作用影响骨矿物质密度

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Osteoporosis is characterized by low bone mineral density (BMD), a highly heritable trait that is determined, in part, by the actions and interactions of multiple genes. Although an increasing number of genes have been identified to have independent effects on BMD, few studies have been performed to identify genes that interact with one another to affect BMD. In this study, we performed gene-gene interaction analyses in selected candidate genes in individuals with extremely high versus low hip BMD (20% tails of the distributions), in two independent U.S. Caucasian samples. The first sample contained 916 unrelated subjects with extreme hip BMD Z-scores selected from a population composed of 2286 subjects. The second sample consisted of 400 unrelated subjects with extreme hip BMD Z-scores selected from a population composed of 1000 subjects. Combining results from these two samples, we found one interacting gene pair (RBMS3 versus ZNF516) which, even after Bonferroni correction for multiple testing, showed consistently significant effects on hip BMD. RMBS3 harbored two single-nucleotide polymorphisms (SNPs), rs6549904 and rs7640046, both of which had significant interactions with an SNP, rs4891159, located on ZNF516 (p = 7.04 ?? 10-11 and 1.03 ?? 10-10). We further validated these results in two additional samples of Caucasian and African descent. The gene pair, RBMS3 versus ZNF516, was successfully replicated in the Caucasian sample (p = 8.07 ?? 10-3 and 2.91 ?? 10 -3). For the African sample, a significant interaction was also detected (p = 0.031 and 0.043), but the direction of the effect was opposite to that observed in the three Caucasian samples. By providing evidence for genetic interactions underlying BMD, this study further delineates the genetic architecture of osteoporosis.
机译:骨质疏松症的特征是骨矿物质密度低(BMD),这是一种高度可遗传的性状,部分由多种基因的作用和相互作用决定。尽管已经鉴定出越来越多的基因对BMD具有独立的作用,但是很少进行研究来鉴定彼此相互作用以影响BMD的基因。在这项研究中,我们在两个独立的美国白种人样本中,对髋部BMD极高与极低(分布的20%尾巴)的个体中的选定候选基因进行了基因-基因相互作用分析。第一个样本包含916位无关的极端髋关节BMD Z评分受试者,这些受试者选自2286名受试者。第二个样本包括400名无关的受试者,这些受试者的髋关节BMD Z得分最高,选自1000名受试者。结合这两个样本的结果,我们发现了一个相互作用的基因对(RBMS3与ZNF516),即使经过Bonferroni校正以进行多次测试,也始终显示出对髋部BMD的显着影响。 RMBS3包含两个单核苷酸多态性(rsnp),即rs6549904和rs7640046,它们与位于ZNF516上的SNP rs4891159具有显着的相互作用(p = 7.04 ?? 10-11和1.03 ?? 10-10)。我们在另外两个白种人和非洲裔样本中进一步验证了这些结果。 RBMS3与ZNF516基因对已在白种人样本中成功复制(p = 8.07×10-3和2.91×10 -3)。对于非洲样品,还检测到了显着的相互作用(p = 0.031和0.043),但作用的方向与在三个高加索样品中观察到的相反。通过提供有关BMD遗传相互作用的证据,本研究进一步描述了骨质疏松症的遗传结构。

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