Ester Audrey R, Tyerman Gayle, Wise Carol A, Blanton Susan H, Hecht Jacqueline T
University of Texas Health Science Center, Houston Graduate School of Biomedical Sciences, Houston, TX, USA.
Clin Orthop Relat Res. 2007 Sep;462:32-7. doi: 10.1097/BLO.0b013e318073c2d9.
Idiopathic talipes equinovarus, also known as clubfoot, is a common birth defect occurring in one of 1000 live births. It is a complex disorder in which multiple genes and environmental factors may play an etiologic role. Several chromosomal deletion regions, including 2q31-33, are associated with talipes equinovarus and may harbor genes that contribute to the idiopathic talipes equinovarus phenotype. Previously, two STRs in the 2q31-33, GATA149B10 and D2S1371, showed linkage with association to idiopathic talipes equinovarus. Single nucleotide polymorphisms (SNPs) in three apoptotic genes (Casp8, Casp10, and CFLAR) near GATA149B10 were genotyped in idiopathic talipes equinovarus families. rs3731714 in Casp10 showed linkage with association, suggesting variation in the apoptotic gene pathway, which is important in limb morphogenesis, and may play a role in the development of idiopathic talipes equinovarus. We genotyped SNPs spanning seven apoptotic genes-Casp3, Casp8, Casp9, Casp10, Bid, Bcl-2 and Apaf1-in 210 simplex trios and 139 multiplex families and tested for link-age and association to idiopathic talipes equinovarus. One SNP in each of the genes provided suggestive evidence of association with idiopathic talipes equinovarus. Several haplotypes constructed from these SNPs displayed altered transmission. These data suggest genetic variation in apoptotic genes may play a role in development of idiopathic talipes equinovarus.
特发性马蹄内翻足,也称为畸形足,是一种常见的出生缺陷,在每1000例活产中就有1例发生。它是一种复杂的疾病,其中多个基因和环境因素可能起病因作用。几个染色体缺失区域,包括2q31 - 33,与马蹄内翻足相关,并且可能包含导致特发性马蹄内翻足表型的基因。此前,2q31 - 33区域的两个短串联重复序列(STR),即GATA149B10和D2S1371,显示出与特发性马蹄内翻足的连锁关联。对GATA149B10附近三个凋亡基因(Casp8、Casp10和CFLAR)中的单核苷酸多态性(SNP)在特发性马蹄内翻足家族中进行了基因分型。Casp10中的rs3731714显示出连锁关联,提示凋亡基因途径中的变异,这在肢体形态发生中很重要,并且可能在特发性马蹄内翻足的发生中起作用。我们对210个核心三联体和139个多重家庭中跨越七个凋亡基因——Casp3、Casp8、Casp9、Casp10、Bid、Bcl - 2和Apaf1——的SNP进行了基因分型,并测试了与特发性马蹄内翻足的连锁和关联。每个基因中的一个SNP提供了与特发性马蹄内翻足相关的提示性证据。由这些SNP构建的几个单倍型显示出传递改变。这些数据表明凋亡基因的遗传变异可能在特发性马蹄内翻足的发生中起作用。