Department of Orthodontics, Dental School, Tongji University, Shanghai, People's Republic of China.
J Dent Res. 2011 Jan;90(1):53-7. doi: 10.1177/0022034510382546. Epub 2010 Nov 1.
Mandibular prognathism is a common dentofacial phenotype with a substantial genetic component; however, few susceptibility loci have been mapped. Ethnicity is a risk factor for mandibular prognathism, and a relatively high prevalence is observed in Asian populations. The hypothesis of this study suggested that a specific locus for mandibular prognathism exists in the Han Chinese population. So, the authors studied a Han Chinese pedigree in which mandibular prognathism was inherited (11 affected, 10 unaffected) in an autosomal dominant pattern. A genomewide linkage scan was performed with the Illumina Linkage-12 DNA Analysis Kit. Multipoint parametric and nonparametric linkage analyses were performed with MERLIN 1.01. A susceptibility locus was identified on chromosome 14q24.3-31.2, with a nonparametric linkage score of 11.341 (empirical P = .020) and a logarithm of the odds score of 2.032 (empirical P = .008). Haplotype analysis refined the candidate locus to a 10.62-cM interval (72.42 to 83.14 cM; 74.57 to 84.66 Mb) between rs1468507 and rs7141857. Within this interval, the candidate functional genes are TGFB3 and LTBP2. In conclusion, the authors detected a suggestive linkage for mandibular prognathism in a Han Chinese pedigree, and this finding can be combined with previous studies to further understand the genetic basis of mandibular prognathism.
下颌前突是一种常见的牙颌面表型,具有重要的遗传成分;然而,已经确定的易感基因位点很少。种族是下颌前突的一个危险因素,在亚洲人群中观察到相对较高的患病率。本研究的假设是,下颌前突在汉族人群中存在一个特定的基因座。因此,作者研究了一个汉族家系,该家系中下颌前突呈常染色体显性遗传(11 例受累,10 例未受累)。使用 Illumina Linkage-12 DNA 分析试剂盒进行全基因组连锁扫描。使用 MERLIN 1.01 进行多点参数和非参数连锁分析。在染色体 14q24.3-31.2 上鉴定到一个易感基因座,非参数连锁得分 11.341(经验 P =.020),对数优势得分 2.032(经验 P =.008)。单体型分析将候选基因座精确定位到 rs1468507 和 rs7141857 之间 10.62-cM 的区间(72.42 至 83.14 cM;74.57 至 84.66 Mb)。在这个区间内,候选功能基因是 TGFB3 和 LTBP2。总之,作者在一个汉族家系中检测到下颌前突的提示性连锁,这一发现可以与以前的研究相结合,进一步了解下颌前突的遗传基础。