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纳格尔综合征:证实SF3B4单倍体不足是主要病因。

Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause.

作者信息

Petit F, Escande F, Jourdain A S, Porchet N, Amiel J, Doray B, Delrue M A, Flori E, Kim C A, Marlin S, Robertson S P, Manouvrier-Hanu S, Holder-Espinasse M

机构信息

Service de Génétique Clinique, Hôpital Jeanne de Flandre, CHRU Lille, Lille, France; Laboratoire de Biologie Moléculaire, Centre de Biologie Pathologie, CHRU Lille, Lille, France; Université Lille Nord de France.

出版信息

Clin Genet. 2014 Sep;86(3):246-51. doi: 10.1111/cge.12259. Epub 2013 Sep 12.

Abstract

Nager syndrome belongs to the group of acrofacial dysostosis, which are characterized by the association of craniofacial and limb malformations. Recently, exome sequencing studies identified the SF3B4 gene as the cause of this condition in most patients. SF3B4 encodes a highly conserved protein implicated in mRNA splicing and bone morphogenic protein (BMP) signaling. We performed SF3B4 sequencing in 14 families (18 patients) whose features were suggestive of Nager syndrome and found nine mutations predicted to result in loss-of-function. SF3B4 is the major gene responsible for autosomal dominant Nager syndrome. All mutations reported predict null alleles, therefore precluding genotype-phenotype correlations. Most mutation-negative patients were phenotypically indistinguishable from patients with mutations, suggesting genetic heterogeneity.

摘要

纳热尔综合征属于肢端颜面发育不全症组,其特征为颅面和肢体畸形并存。最近,外显子组测序研究确定SF3B4基因是大多数患者患此病的病因。SF3B4编码一种高度保守的蛋白质,参与mRNA剪接和骨形态发生蛋白(BMP)信号传导。我们对14个家系(18名患者)进行了SF3B4测序,这些家系的特征提示为纳热尔综合征,结果发现9个预测会导致功能丧失的突变。SF3B4是常染色体显性纳热尔综合征的主要致病基因。所有报道的突变均预测为无效等位基因,因此无法进行基因型与表型的关联分析。大多数未检测到突变的患者在表型上与有突变的患者无法区分,提示存在遗传异质性。

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