• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

检测 8q24 中的标记物,以解释亚洲人和欧洲人之间具有/不具有腭裂的唇裂关联证据存在差异的原因。

Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans.

机构信息

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland 21205, USA.

出版信息

Genet Epidemiol. 2012 May;36(4):392-9. doi: 10.1002/gepi.21633. Epub 2012 Apr 16.

DOI:10.1002/gepi.21633
PMID:22508319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3615645/
Abstract

In a recent genome-wide association study (GWAS) from an international consortium, evidence of linkage and association in chr8q24 was much stronger among nonsyndromic cleft lip/palate (CL/P) case-parent trios of European ancestry than among trios of Asian ancestry. We examined marker information content and haplotype diversity across 13 recruitment sites (from Europe, United States, and Asia) separately, and conducted principal components analysis (PCA) on parents. As expected, PCA revealed large genetic distances between Europeans and Asians, and a north-south cline from Korea to Singapore in Asia, with Filipino parents forming a somewhat distinct Southeast Asian cluster. Hierarchical clustering of SNP heterozygosity revealed two major clades consistent with PCA results. All genotyped SNPs giving P < 10(-6) in the allelic transmission disequilibrium test (TDT) showed higher heterozygosity in Europeans than Asians. On average, European ancestry parents had higher haplotype diversity than Asians. Imputing additional variants across chr8q24 increased the strength of statistical evidence among Europeans and also revealed a significant signal among Asians (although it did not reach genome-wide significance). Tests for SNP-population interaction were negative, indicating the lack of strong signal for 8q24 in families of Asian ancestry was not due to any distinct genetic effect, but could simply reflect low power due to lower allele frequencies in Asians.

摘要

在最近一项国际合作的全基因组关联研究(GWAS)中,非综合征性唇腭裂(CL/P)病例-父母三体型中 8q24 区域的连锁和关联证据在欧洲血统的三体型中比在亚洲血统的三体型中要强得多。我们分别检查了来自欧洲、美国和亚洲的 13 个招募点的标记信息含量和单倍型多样性,并对父母进行了主成分分析(PCA)。如预期的那样,PCA 揭示了欧洲人和亚洲人之间的巨大遗传距离,以及亚洲从韩国到新加坡的南北渐变,菲律宾父母形成了一个相对独特的东南亚集群。SNP 杂合性的层次聚类揭示了两个与 PCA 结果一致的主要分支。在等位基因传递不平衡测试(TDT)中,所有 P < 10(-6) 的基因分型 SNP 都显示出欧洲人的杂合度高于亚洲人。平均而言,欧洲血统的父母比亚洲人的单倍型多样性更高。在 chr8q24 上推断额外的变体增加了欧洲人之间统计证据的强度,也揭示了亚洲人之间的显著信号(尽管它没有达到全基因组的显著性)。SNP-人群相互作用的测试为阴性,这表明亚洲血统的家族中 8q24 没有强烈的信号,不是由于任何独特的遗传效应,而是由于亚洲人的等位基因频率较低,可能只是反映了低功效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/20acd3bdd613/nihms409566f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/7da07523c96c/nihms409566f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/45b3b331b4bb/nihms409566f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/f9604f4ada27/nihms409566f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/e3e996591e8e/nihms409566f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/20acd3bdd613/nihms409566f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/7da07523c96c/nihms409566f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/45b3b331b4bb/nihms409566f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/f9604f4ada27/nihms409566f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/e3e996591e8e/nihms409566f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1b3/3615645/20acd3bdd613/nihms409566f5.jpg

相似文献

1
Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans.检测 8q24 中的标记物,以解释亚洲人和欧洲人之间具有/不具有腭裂的唇裂关联证据存在差异的原因。
Genet Epidemiol. 2012 May;36(4):392-9. doi: 10.1002/gepi.21633. Epub 2012 Apr 16.
2
Association between PAX9 single-nucleotide polymorphisms and nonsyndromic cleft lip with or without cleft palate.PAX9单核苷酸多态性与非综合征性唇裂伴或不伴腭裂之间的关联。
J Craniofac Surg. 2012 Sep;23(5):1262-6. doi: 10.1097/SCS.0b013e31824e27c7.
3
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry.巴西一个非洲血统比例高的人群中,非综合征性唇裂伴或不伴腭裂的遗传风险因素。
Am J Med Genet A. 2015 Oct;167A(10):2344-9. doi: 10.1002/ajmg.a.37181. Epub 2015 Jul 22.
4
Association between MSX1 SNPs and nonsyndromic cleft lip with or without cleft palate in the Korean population.MSX1 单核苷酸多态性与韩国人群中非综合征性唇裂伴或不伴腭裂的关联。
J Korean Med Sci. 2013 Apr;28(4):522-6. doi: 10.3346/jkms.2013.28.4.522. Epub 2013 Mar 27.
5
Investigation of Parental Transmission of RUNX2 Single Nucleotide Polymorphism and Its Association With Nonsyndromic Cleft Lip With or Without Palate.RUNX2单核苷酸多态性的亲代传递及其与非综合征性唇裂伴或不伴腭裂的关联研究
Cleft Palate Craniofac J. 2014 Mar;51(2):234-9. doi: 10.1597/12-312. Epub 2013 Aug 2.
6
Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.对来自三个群体的口腔腭裂病例-父母三联体中2号染色体上的候选基因进行分析。
Hum Genet. 2006 Nov;120(4):501-18. doi: 10.1007/s00439-006-0235-9. Epub 2006 Sep 5.
7
Genetic effect of transforming growth factor alpha gene variants on the risk of nonsyndromic cleft lip with or without palate in korean populations.转化生长因子α基因变异对韩国人群非综合征性唇裂伴或不伴腭裂风险的遗传效应。
Cleft Palate Craniofac J. 2015 May;52(3):293-300. doi: 10.1597/13-067. Epub 2014 May 7.
8
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.一项关于唇裂伴或不伴腭裂的全基因组关联研究鉴定了 MAFB 和 ABCA4 附近的风险变异。
Nat Genet. 2010 Jun;42(6):525-9. doi: 10.1038/ng.580. Epub 2010 May 2.
9
Joint testing of genotypic and gene-environment interaction identified novel association for BMP4 with non-syndromic CL/P in an Asian population using data from an International Cleft Consortium.利用国际腭裂联盟的数据,对基因型和基因-环境相互作用进行联合检测,在亚洲人群中发现了骨形态发生蛋白4(BMP4)与非综合征性唇腭裂(CL/P)之间的新关联。
PLoS One. 2014 Oct 10;9(10):e109038. doi: 10.1371/journal.pone.0109038. eCollection 2014.
10
Genetic associations and parent-of-origin effects of PVRL1 in non-syndromic cleft lip with or without cleft palate across multiple ethnic populations.多个种族群体中非综合征性唇裂伴或不伴腭裂中 PVRL1 的遗传关联和母源效应。
Epidemiol Health. 2024;46:e2024069. doi: 10.4178/epih.e2024069. Epub 2024 Aug 9.

引用本文的文献

1
Genetic-epigenetic interactions (meQTLs) in orofacial clefts etiology.口腔颌面部裂隙病因中的遗传-表观遗传相互作用(meQTLs)
medRxiv. 2025 Feb 12:2025.02.09.25321494. doi: 10.1101/2025.02.09.25321494.
2
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.多民族家庭与对照样本中非综合征性口面部裂隙的全基因组关联研究确定了新区域。
Front Cell Dev Biol. 2021 Apr 9;9:621482. doi: 10.3389/fcell.2021.621482. eCollection 2021.
3
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21.来自 Gabriella Miller 儿童第一儿科研究联合会的口腔颌面裂三巨头的全基因组测序确定了 21 号染色体上的一个新位点。
Hum Genet. 2020 Feb;139(2):215-226. doi: 10.1007/s00439-019-02099-1. Epub 2019 Dec 17.
4
Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation.六个非综合征型唇腭裂基因座与正常范围的颅面变异相关。
Front Genet. 2018 Oct 25;9:502. doi: 10.3389/fgene.2018.00502. eCollection 2018.
5
Proportion of Orofacial Clefts Attributable to Recognized Risk Factors.可归因于已确认风险因素的口面部裂隙比例。
Cleft Palate Craniofac J. 2019 Feb;56(2):151-158. doi: 10.1177/1055665618774019. Epub 2018 May 4.
6
Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing.通过靶向测序鉴定口面裂畸形表型异质性的遗传来源。
Birth Defects Res. 2017 Jul 17;109(13):1030-1038. doi: 10.1002/bdr2.23605.
7
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.全基因组分析非综合征性唇腭裂发现 14 个新位点和遗传异质性。
Nat Commun. 2017 Feb 24;8:14364. doi: 10.1038/ncomms14364.
8
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.非综合征性口面部裂隙的全基因组荟萃分析确定了FOXE1与所有口面部裂隙之间以及TP63与伴或不伴腭裂的唇裂之间的新关联。
Hum Genet. 2017 Mar;136(3):275-286. doi: 10.1007/s00439-016-1754-7. Epub 2017 Jan 4.
9
Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunities.影响口腔颌面裂隙风险的遗传因素:当今的挑战与未来的机遇。
F1000Res. 2016 Nov 30;5:2800. doi: 10.12688/f1000research.9503.1. eCollection 2016.
10
Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations.关联研究和直接DNA测序表明撒哈拉以南非洲人群非综合征性口面部裂隙病因中的遗传易感位点。
J Dent Res. 2016 Oct;95(11):1245-56. doi: 10.1177/0022034516657003. Epub 2016 Jul 1.

本文引用的文献

1
Incorporating genotype uncertainties into the genotypic TDT for main effects and gene-environment interactions.将基因型不确定性纳入主效应和基因-环境相互作用的基因型 TDT 中。
Genet Epidemiol. 2012 Apr;36(3):225-34. doi: 10.1002/gepi.21615.
2
Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation.基于精确分析参数估计的病例-双亲三联体数据中SNP和基因-环境相互作用的快速检测。
Biometrics. 2012 Sep;68(3):766-73. doi: 10.1111/j.1541-0420.2011.01713.x. Epub 2011 Dec 7.
3
A map of human genome variation from population-scale sequencing.人类基因组变异的图谱来自于基于人群的测序。
Nature. 2010 Oct 28;467(7319):1061-73. doi: 10.1038/nature09534.
4
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.中美洲人群非综合征性唇裂伴或不伴腭裂的遗传风险因素:IRF6以及8q24和10q25处变异的证据
Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):535-7. doi: 10.1002/bdra.20689.
5
Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population.波兰人群中已报道的候选基因或区域的遗传变异与唇裂伴或不伴腭裂风险之间的关联。
Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):538-45. doi: 10.1002/bdra.20687.
6
8q24 prostate, breast, and colon cancer risk loci show tissue-specific long-range interaction with MYC.8q24前列腺癌、乳腺癌和结肠癌风险位点显示与MYC存在组织特异性的长程相互作用。
Proc Natl Acad Sci U S A. 2010 May 25;107(21):9742-6. doi: 10.1073/pnas.0910668107. Epub 2010 May 7.
7
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.一项关于唇裂伴或不伴腭裂的全基因组关联研究鉴定了 MAFB 和 ABCA4 附近的风险变异。
Nat Genet. 2010 Jun;42(6):525-9. doi: 10.1038/ng.580. Epub 2010 May 2.
8
Family-based study shows heterogeneity of a susceptibility locus on chromosome 8q24 for nonsyndromic cleft lip and palate.基于家系的研究表明,8号染色体q24区域上一个非综合征性唇腭裂易感基因座存在异质性。
Birth Defects Res A Clin Mol Teratol. 2010 Apr;88(4):256-9. doi: 10.1002/bdra.20659.
9
Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients.爱沙尼亚和立陶宛患者中8号染色体q24区域非综合征性唇裂伴或不伴腭裂新易感基因座的复制研究
Am J Med Genet A. 2009 Nov;149A(11):2551-3. doi: 10.1002/ajmg.a.33024.
10
A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.一项全基因组关联研究在 8q24 上确定了非综合征型唇裂伴或不伴腭裂的一个位点。
J Pediatr. 2009 Dec;155(6):909-13. doi: 10.1016/j.jpeds.2009.06.020. Epub 2009 Aug 4.