Moreno Lina M, Arcos-Burgos Mauricio, Marazita Mary L, Krahn Katherine, Maher Brion S, Cooper Margaret E, Valencia-Ramirez Consuelo R, Lidral Andrew C
Dows Institute for Dental Research, University of Iowa, Iowa City, Iowa 52242, USA.
Am J Med Genet A. 2004 Mar 1;125A(2):135-44. doi: 10.1002/ajmg.a.20425.
Non-syndromic cleft lip with or without cleft palate (CL/P) is a genetically complex birth defect, with a prevalence from 1/500 to 1/1,000 live births. Evidence from linkage and linkage disequilibrium studies is contradictory suggesting that heterogeneity between study populations may exist. A recent report of a genome widescan in 92 sib pairs from the United Kingdom revealed suggestive linkage to 10 loci [Prescott et al., 2000]. The purpose of this study is to replicate those results and evaluate additional candidate genes in 49 Colombian and 13 Ohio families. Genotypes were obtained for STRPs at 1p36, 2p13 (TGFA), 4p16 (MSX1), 6p23-25, 6q25-27, 8q23-24, 11p12-q13, 12q13, 14q24 (TGFB3), 16q22-24, 17q12-21 (RARA), and Xcen-q21. Linkage was performed using parametric (dominant and recessive models) and non-parametric (GenehunterNPL and SimIBD) analyses. In addition, heterogeneity was analyzed using GenehunterHLOD, and association determined by the TDT. The Colombian families showed significant SimIBD results for 11p12-q13 (P = 0.034), 12q13 (P = 0.015), 16q22-24 (0.01), and 17q12-21 (0.009), while the Ohio families showed significant SimIBD results for 1p36 (P = 0.02), TGFA (P = 0.005), 6p23 (P = 0.004), 11p12-q13 (P = 0.048) and significant NPL results for TGFA (NPL = 3.01, P = 0.009), 4p16 (MNPL = 2.07, P = 0.03) and 12q13 (SNPL = 3.55, P = 0.007). Significant association results were obtained only for the Colombian families in the regions 1p36 (P = 0.046), 6p23-25 (P = 0.020), and 12q13 (P = 0.046). In addition several families yielded LOD scores ranging from 1.09 to 1.73, for loci at 4p16, 6p23-25, 16q22-24, and 17q13. These results confirm previous reports for these loci. However, the differences between the two populations suggest that population specific locus heterogeneity exists. This article contains supplementary material, which may be viewed at the American Journal of Medical Genetics website at http://www.interscience.wiley.com/jpages/0148-7299/suppmat/index.html.
非综合征性唇裂伴或不伴腭裂(CL/P)是一种具有遗传复杂性的出生缺陷,在活产婴儿中的患病率为1/500至1/1000。连锁分析和连锁不平衡研究的证据相互矛盾,这表明研究人群之间可能存在异质性。最近一份对来自英国的92对同胞进行全基因组扫描的报告显示,与10个基因座存在提示性连锁关系[普雷斯科特等人,2000年]。本研究的目的是重复这些结果,并评估49个哥伦比亚家庭和13个俄亥俄家庭中的其他候选基因。获取了位于1p36、2p13(TGFA)、4p16(MSX1)、6p23 - 25、6q25 - 27、8q23 - 24、11p12 - q13、12q13、14q24(TGFB3)、16q22 - 24、17q12 - 21(RARA)和Xcen - q21的STRP的基因型。使用参数分析(显性和隐性模型)和非参数分析(Genehunter NPL和SimIBD)进行连锁分析。此外,使用Genehunter HLOD分析异质性,并通过TDT确定关联性。哥伦比亚家庭在11p12 - q13(P = 0.034)、12q13(P = 0.015)、16q22 - 24(0.01)和17q12 - 21(0.009)处显示出显著的SimIBD结果,而俄亥俄家庭在1p36(P = 0.02)、TGFA(P = 0.005)、6p23(P = 0.004)、11p12 - q13(P = 0.048)处显示出显著的SimIBD结果,并且在TGFA(NPL = 3.01,P = 0.009)、4p16(MNPL = 2.07,P = 0.03)和12q13(SNPL = 3.55,P = 0.007)处显示出显著的NPL结果。仅在哥伦比亚家庭的1p36(P = 0.046)、6p23 - 25(P = 0.020)和12q13(P = 0.046)区域获得了显著的关联结果。此外,几个家庭在4p16、6p23 - 25、16q22 - 24和17q13的基因座上产生了1.09至1.73的LOD分数。这些结果证实了先前关于这些基因座的报告。然而,这两个人群之间的差异表明存在人群特异性的基因座异质性。本文包含补充材料,可在美国医学遗传学杂志网站http://www.interscience.wiley.com/jpages/0148 - 7299/suppmat/index.html上查看。