Félix Têmis M, Hanshaw Benjamin C, Mueller Robert, Bitoun Pierre, Murray Jeffrey C
Department of Pediatrics, University of Iowa, Iowa City, IA 52242, USA.
Am J Med Genet A. 2006 Oct 1;140(19):2110-4. doi: 10.1002/ajmg.a.31308.
Cleft lip and palate is a common birth defect that has a complex etiology resulting from an interaction of genetic and environmental factors. Few genes are known to contribute to its etiology. CHARGE syndrome is a common multiple malformation syndrome in which 20-36% of the cases have clefting. CHARGE is caused by mutations or deletions in the CHD7 gene. We analyzed the coding regions of CHD7 in nine CHARGE cases and identified five mutations, four of which were novel. We sequenced selected CHD7 exons in non-syndromic clefting cases from Iowa and Philippines populations, as well as matched controls. Variants in non-syndromic cases were found, however, the numbers were not statistically different from the controls. Association analysis of three single nucleotide polymorphisms (SNPs) using 878 case-parent triads from Iowa and Philippines population showed no significant overtransmission. Mutations in CHD7 are not common in isolated clefting cases and we found minimal evidence that CHD7 can act as a modifier for non-syndromic clefting.
唇腭裂是一种常见的出生缺陷,其病因复杂,是由遗传和环境因素相互作用导致的。已知很少有基因会导致其发病。CHARGE综合征是一种常见的多发畸形综合征,其中20% - 36%的病例有腭裂。CHARGE综合征是由CHD7基因突变或缺失引起的。我们分析了9例CHARGE综合征病例中CHD7的编码区,鉴定出5个突变,其中4个是新发现的。我们对来自爱荷华州和菲律宾人群的非综合征性腭裂病例以及匹配的对照进行了选定CHD7外显子的测序。在非综合征性病例中发现了变异,但数量与对照无统计学差异。使用来自爱荷华州和菲律宾人群的878个病例 - 父母三联体对三个单核苷酸多态性(SNP)进行关联分析,结果显示无显著的过度传递。CHD7突变在孤立性腭裂病例中并不常见,我们发现几乎没有证据表明CHD7可作为非综合征性腭裂的修饰基因。