New insights from GWAS for the cleft palate among han Chinese population

S. Duan, Ning Huang, Bihe Zhang, Jia‐yu Shi, Shan He, Jian Ma, Qiongqiong Yu, B. Shi, Z. Jia
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引用次数: 19

Abstract

Background Genome wide association studies (GWAS) already have identified tens of susceptible loci for nonsyndromic cleft lip with or without cleft palate (NSCL/P). However, whether these loci associated with nonsyndromic cleft palate only (NSCPO) remains unknown. Material and Methods In this study, we replicated 38 SNPs (Single nucleotide polymorphisms) which has the most significant p values in published GWASs, genotyping by using SNPscan among 144 NSCPO trios from Western Han Chinese. We performed the transmission disequilibrium test (TDT) on individual SNPs and gene-gene (GxG) interaction analyses on the family data; Parent-of-Origin effects were assessed by separately considering transmissions from heterozygous fathers versus heterozygous mothers to affected offspring. Results Allelic TDT results showed that T allele at rs742071 (PAX7) (p=0.025, ORtransmission=3.00, 95%CI: 1.09-8.25) and G allele at rs2485893 (10kb 3’ of SYT14) were associated with NSCPO (p=0.0036, ORtransmission= 0.60, 95%CI: 0.42-0.85). Genotypic TDT based on 3 pseudo controls further confirmed that rs742071 (p-value=0.03, ORtransmission=3.00, 95%CI: 1.09-8.25) and rs2485893 were associated with NSCPO under additive model (p-value= 0.02, ORtransmission= 0.66, 95%CI: 0.47-0.92). Genotypic TDT for epistatic interactions showed that rs4844913 (37kb 3’ of DIEXF) interacted with rs11119388 (SYT14) (p-value=1.80E-08) and rs6072081 (53kb 3’ of MAFB) interacted with rs6102085 (33kb 3’ of MAFB) (p-value=3.60E-04) for NSCPO, suggesting they may act in the same pathway in the etiology of NSCPO. Conclusions In this study, we found that rs742071 and rs2485893 were associated NSCPO from Han Chinese population; also, interactions of rs4844913:rs11119388 and rs6072081:rs6102085 for NSCPO were identified, gene-gene interactions have been proposed as a potential source of the remaining heritability, these findings provided new insights of the previous GWAS. Key words:GWAS, NSCPO, TDT, parent-of-origin effects, epistatic interactions.
GWAS对汉族腭裂的新认识
基因组全关联研究(GWAS)已经确定了数十个非综合征性唇裂伴或不伴腭裂(NSCL/P)易感位点。然而,这些基因座是否与单纯非综合征性腭裂(NSCPO)相关尚不清楚。材料与方法本研究利用SNPscan对144例西汉NSCPO三人组进行基因分型,复制了已发表的GWASs中p值最高的38个snp(单核苷酸多态性)。我们对个体snp进行了传递不平衡检验(TDT),并对家族数据进行了基因-基因(GxG)互作分析;通过单独考虑杂合父亲与杂合母亲对受影响后代的传播来评估原生父母效应。结果等位基因TDT结果显示,rs742071位点(PAX7)的T等位基因(p=0.025, or传率=3.00,95%CI: 1.09 ~ 8.25)和rs2485893位点(SYT14位点10kb 3′)的G等位基因(p=0.0036, or传率= 0.60,95%CI: 0.42 ~ 0.85)与NSCPO相关。基于3个伪对照的基因型TDT进一步证实了rs742071 (p值=0.03,ORtransmission=3.00, 95%CI: 1.09 ~ 8.25)和rs2485893在加性模型下与NSCPO相关(p值= 0.02,ORtransmission= 0.66, 95%CI: 0.47 ~ 0.92)。基因型TDT显示,rs4844913 (DIEXF的37kb 3 ')与rs11119388 (SYT14)相互作用(p值=1.80E-08), rs6072081 (MAFB的53kb 3 ')与rs6102085 (MAFB的33kb 3 ')相互作用(p值=3.60E-04),提示它们在NSCPO的病因学中可能通过相同的途径起作用。结论本研究发现,rs742071和rs2485893与汉族人群NSCPO相关;此外,还发现了rs4844913:rs11119388和rs6072081:rs6102085对NSCPO的相互作用,基因-基因相互作用被认为是剩余遗传力的潜在来源,这些发现为之前的GWAS提供了新的见解。关键词:GWAS, NSCPO, TDT,亲本效应,上位相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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