Hikida Masanori, Tsuda Masayoshi, Watanabe Akira, Kinoshita Akira, Akita Sadanori, Hirano Akiyoshi, Uchiyama Takeshi, Yoshiura Koh-ichiro
Department of Oral and Maxillofacial Surgery, Tokyo Dental College, Chiba, Japan.
Cleft Palate Craniofac J. 2012 Nov;49(6):714-7. doi: 10.1597/10-242. Epub 2011 Oct 7.
Recent genome-wide association studies identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate (NSCL±P) on 8q24.21, 10q25.3, 13q31.1, 15q13.3, 17q22, and 18q22 in populations of European origin. The purpose of this study was to determine, using DNA samples, whether 8q24.21 was a susceptibility locus for the development of NSCL±P in Japanese patients.
We used DNA from 167 Japanese NSCL±P patients (45 cleft lip without cleft palate and 122 cleft lip with cleft palate patients) and 190 Japanese unaffected control individuals. We performed an association study using 13 single nucleotide polymorphisms (SNPs) selected on the 8q24.21 locus. Genotyping of each SNP was carried out by direct sequencing of genomic DNA. Additionally, a haplotype block was constructed using the selected SNPs.
The 13 selected SNPs were successfully genotyped in 357 individuals. The p values obtained were not low enough to indicate a significant association between the haplotypes and the development of NSCL±P in this population.
Our results suggest that the 8q24.21 locus is not associated with susceptibility to NSCL±P in Japanese patients and provide further evidence that ethnicity is a strong factor in determining susceptibility loci, albeit using a limited number of samples. Further studies are needed to identify regions involved in the development of NSCL±P in the Japanese population.
近期全基因组关联研究在欧洲裔人群中确定了8q24.21、10q25.3、13q31.1、15q13.3、17q22和18q22为非综合征性唇裂伴或不伴腭裂(NSCL±P)的易感基因座。本研究的目的是使用DNA样本确定8q24.21是否为日本患者发生NSCL±P的易感基因座。
我们使用了167例日本NSCL±P患者(45例单纯唇裂和122例唇裂伴腭裂患者)以及190例未受影响的日本对照个体的DNA。我们使用在8q24.21基因座上选择的13个单核苷酸多态性(SNP)进行了关联研究。通过对基因组DNA进行直接测序对每个SNP进行基因分型。此外,使用选定的SNP构建单倍型块。
在357名个体中成功对13个选定的SNP进行了基因分型。获得的p值不够低,不足以表明该人群中这些单倍型与NSCL±P发生之间存在显著关联。
我们的结果表明,8q24.21基因座与日本患者NSCL±P的易感性无关,并提供了进一步的证据,即种族是确定易感基因座的一个重要因素,尽管样本数量有限。需要进一步研究以确定日本人群中参与NSCL±P发生发展的区域。