Department of Medical Genetics, University of Calgary, Calgary, Alberta, Canada.
Am J Hum Genet. 2012 May 4;90(5):925-33. doi: 10.1016/j.ajhg.2012.04.004. Epub 2012 Apr 26.
Nager syndrome, first described more than 60 years ago, is the archetype of a class of disorders called the acrofacial dysostoses, which are characterized by craniofacial and limb malformations. Despite intensive efforts, no gene for Nager syndrome has yet been identified. In an international collaboration, FORGE Canada and the National Institutes of Health Centers for Mendelian Genomics used exome sequencing as a discovery tool and found that mutations in SF3B4, a component of the U2 pre-mRNA spliceosomal complex, cause Nager syndrome. After Sanger sequencing of SF3B4 in a validation cohort, 20 of 35 (57%) families affected by Nager syndrome had 1 of 18 different mutations, nearly all of which were frameshifts. These results suggest that most cases of Nager syndrome are caused by haploinsufficiency of SF3B4. Our findings add Nager syndrome to a growing list of disorders caused by mutations in genes that encode major components of the spliceosome and also highlight the synergistic potential of international collaboration when exome sequencing is applied in the search for genes responsible for rare Mendelian phenotypes.
Nager 综合征,首先于 60 多年前描述,是一类称为颅面发育不全的疾病的典型范例,其特征为颅面和肢体畸形。尽管进行了深入研究,但尚未鉴定出 Nager 综合征的基因。在一项国际合作中,加拿大 FORGE 和美国国立卫生研究院孟德尔基因组学中心使用外显子组测序作为发现工具,发现 U2 前体 mRNA 剪接体复合物的组成部分 SF3B4 的突变导致 Nager 综合征。在验证队列中对 SF3B4 进行 Sanger 测序后,35 个受 Nager 综合征影响的家庭中有 20 个(57%)有 18 种不同突变中的 1 种,几乎所有突变都是移码。这些结果表明,大多数 Nager 综合征病例是由 SF3B4 的单倍不足引起的。我们的研究结果将 Nager 综合征添加到由编码剪接体主要成分的基因突变引起的一系列疾病中,并且还突出了外显子组测序在寻找导致罕见孟德尔表型的基因时国际合作的协同潜力。