| Literature DB >> 26256109 |
Tianhua Niu1, Ning Liu2, Xun Yu2, Ming Zhao1, Hyung Jin Choi3,4, Paul J Leo5, Matthew A Brown5, Lei Zhang1,6, Yu-Fang Pei1, Hui Shen1, Hao He1, Xiaoying Fu1, Shan Lu2, Xiang-Ding Chen2, Li-Jun Tan2, Tie-Lin Yang7, Yan Guo7, Nam H Cho8, Jie Shen9, Yan-Fang Guo9, Geoffrey C Nicholson10, Richard L Prince11,12, John A Eisman13, Graeme Jones14, Philip N Sambrook15, Qing Tian1, Xue-Zhen Zhu7, Christopher J Papasian16, Emma L Duncan5,17, André G Uitterlinden18,19,20, Chan Soo Shin3, Shuanglin Xiang2, Hong-Wen Deng1,2.
Abstract
Protein phosphorylation regulates a wide variety of cellular processes. Thus, we hypothesize that single-nucleotide polymorphisms (SNPs) that may modulate protein phosphorylation could affect osteoporosis risk. Based on a previous conventional genome-wide association (GWA) study, we conducted a three-stage meta-analysis targeting phosphorylation-related SNPs (phosSNPs) for femoral neck (FN)-bone mineral density (BMD), total hip (HIP)-BMD, and lumbar spine (LS)-BMD phenotypes. In stage 1, 9593 phosSNPs were meta-analyzed in 11,140 individuals of various ancestries. Genome-wide significance (GWS) and suggestive significance were defined by α = 5.21 × 10(-6) (0.05/9593) and 1.00 × 10(-4), respectively. In stage 2, nine stage 1-discovered phosSNPs (based on α = 1.00 × 10(-4)) were in silico meta-analyzed in Dutch, Korean, and Australian cohorts. In stage 3, four phosSNPs that replicated in stage 2 (based on α = 5.56 × 10(-3), 0.05/9) were de novo genotyped in two independent cohorts. IDUA rs3755955 and rs6831280, and WNT16 rs2707466 were associated with BMD phenotypes in each respective stage, and in three stages combined, achieving GWS for both FN-BMD (p = 8.36 × 10(-10), p = 5.26 × 10(-10), and p = 3.01 × 10(-10), respectively) and HIP-BMD (p = 3.26 × 10(-6), p = 1.97 × 10(-6), and p = 1.63 × 10(-12), respectively). Although in vitro studies demonstrated no differences in expressions of wild-type and mutant forms of IDUA and WNT16B proteins, in silico analyses predicts that WNT16 rs2707466 directly abolishes a phosphorylation site, which could cause a deleterious effect on WNT16 protein, and that IDUA phosSNPs rs3755955 and rs6831280 could exert indirect effects on nearby phosphorylation sites. Further studies will be required to determine the detailed and specific molecular effects of these BMD-associated non-synonymous variants.Entities:
Keywords: HUMAN ASSOCIATION STUDIES; META-ANALYSIS; OSTEOPOROSIS; SINGLE-NUCLEOTIDE POLYMORPHISM; WNT/BETA-CATENIN/LRPS
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Year: 2015 PMID: 26256109 PMCID: PMC5362379 DOI: 10.1002/jbmr.2687
Source DB: PubMed Journal: J Bone Miner Res ISSN: 0884-0431 Impact factor: 6.741