el Ghouzzi V, Le Merrer M, Perrin-Schmitt F, Lajeunie E, Benit P, Renier D, Bourgeois P, Bolcato-Bellemin A L, Munnich A, Bonaventure J
Unité Recherches sur les Handicaps Génétiques de l'Enfant INSERM U-393, Institut Necker, Paris, France.
Nat Genet. 1997 Jan;15(1):42-6. doi: 10.1038/ng0197-42.
Saethre-Chotzen syndrome (acrocephalo-syndactyly type III, ACS III) is an autosomal dominant craniosynostosis with brachydactyly, soft tissue syndactyly and facial dysmorphism including ptosis, facial asymmetry and prominent ear crura. ACS III has been mapped to chromosome 7p21-22. Of interest, TWIST, the human counterpart of the murine Twist gene, has been localized on chromosome 7p21 as well. The Twist gene product is a transcription factor containing a basic helix-loop-helix (b-HLH) domain, required in head mesenchyme for cranial neural tube morphogenesis in mice. The co-localisation of ACS III and TWIST prompted us to screen ACS III patients for TWIST gene mutations especially as mice heterozygous for Twist null mutations displayed skull defects and duplication of hind leg digits. Here, we report 21-bp insertions and nonsense mutations of the TWIST gene (S127X, E130X) in seven ACS III probands and describe impairment of head mesenchyme induction by TWIST as a novel pathophysiological mechanism in human craniosynostoses.
塞特勒-乔岑综合征(III型尖头并指畸形,ACS III)是一种常染色体显性颅缝早闭症,伴有短指畸形、软组织并指畸形以及面部畸形,包括上睑下垂、面部不对称和耳轮突出。ACS III已被定位到染色体7p21 - 22。有趣的是,小鼠Twist基因在人类中的对应基因TWIST也定位于染色体7p21。Twist基因产物是一种转录因子,包含一个碱性螺旋-环-螺旋(b - HLH)结构域,在小鼠头部间充质中对颅神经管形态发生是必需的。ACS III与TWIST的共定位促使我们对ACS III患者进行TWIST基因突变筛查,特别是因为Twist基因无效突变的杂合小鼠表现出颅骨缺陷和后腿趾重复。在此,我们报告了7例ACS III先证者中TWIST基因的21bp插入和无义突变(S127X、E130X),并将TWIST对头间充质诱导的损害描述为人类颅缝早闭症中的一种新的病理生理机制。