4.6 Article

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

期刊

JOURNAL OF BONE AND MINERAL RESEARCH
卷 28, 期 4, 页码 828-837

出版社

WILEY-BLACKWELL
DOI: 10.1002/jbmr.1788

关键词

INTERACTION; ASSOCIATION; BMD; OSTEOPOROSIS

资金

  1. National Natural Science Foundation of China [81000363, 31000554]
  2. NIH [R01 AR050496, R21 AG027110, R01 AG026564, P50 AR055081, R01 AR057049-01A1, R21 AA015973]
  3. Fundamental Research Funds for the Central Universities
  4. PhD. Programs Foundation of Ministry of Education of China [20100201120058]
  5. Shanghai Leading Academic Discipline Project [S30501]
  6. Ministry of Education
  7. University of Shanghai for Science and Technology
  8. Xi'an Jiaotong University
  9. Ministry of Education of China
  10. NIH's National Heart, Lung, and Blood Institute (NHLBI)
  11. Boston University [N01-HC-25195]
  12. NHLBI [N01WH22110, 24152, 32100-2, 32105-6, 32108-9, 32111-13, 32115, 32118-32119, 32122, 42107-26, 42129-32, 44221]

向作者/读者索取更多资源

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=7.04x1011 and 1.03x1010). 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=8.07x103 and 2.91x103). 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. (c) 2013 American Society for Bone and Mineral Research.

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