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PMID: 14981713 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio.

American journal of medical genetics. Part A ·Vol. 125A ·No. 2 ·2004-03-01 ·页码 135-44

Moreno LM, Arcos-Burgos M, Marazita ML, Krahn K, Maher BS, Cooper ME, Valencia-Ramirez CR, Lidral AC

Abstract

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.

MeSH 主题词
Cleft Lip/genetics,pathology Cleft Palate/genetics,pathology Colombia Family Health Female Genes, Dominant Genes, Recessive Genetic Linkage/genetics Genetic Markers Genetic Predisposition to Disease/genetics Genotype Humans Lod Score Male Microsatellite Repeats Ohio Pedigree Prevalence
化学物质
Genetic Markers
作者与单位
共 8 位作者,点击展开单位 / ORCID
Moreno Lina M
Dows Institute for Dental Research, University of Iowa, Iowa City, Iowa 52242, USA.
Arcos-Burgos Mauricio
Marazita Mary L
Krahn Katherine
Maher Brion S
Cooper Margaret E
Valencia-Ramirez Consuelo R
Lidral Andrew C
Article Info
Journal
American journal of medical genetics. Part A
Abbr.
Am J Med Genet A
ISSN
1552-4825
Published
2004-03-01
页码
135-44
Language
English
Country/Region
United States
NLM ID
101235741
基金资助
NIDCR NIH HHS · K02 DE015291-05 · United States
NIDCR NIH HHS · R03 DE012533-02 · United States
NIDCR NIH HHS · R01 DE014667-06 · United States
NIDCR NIH HHS · K02 DE015291-01 · United States
NIDCR NIH HHS · R01 DE014667 · United States
NIDCR NIH HHS · R01 DE014667-02 · United States
NIDCR NIH HHS · K02 DE015291-02 · United States
NIDCR NIH HHS · R01 DE014667-03 · United States
NIDCR NIH HHS · P60 DE13076 · United States
NIDCR NIH HHS · R01 DE016148 · United States
NIDCR NIH HHS · R01 DE014667-08 · United States
NIDCR NIH HHS · R01 DE014667-04 · United States
NIDCR NIH HHS · K02 DE015291-03 · United States
NIDCR NIH HHS · R01 DE014667-07 · United States
NIDCR NIH HHS · R01 DE014667-05 · United States
NIDCR NIH HHS · K02 DE015291 · United States
NIDCR NIH HHS · R01 DE 14677 · United States
NIDCR NIH HHS · K02 DE015291-04 · United States
NIDCR NIH HHS · R01 DE014667-01 · United States
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