Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome

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• 作者：Nisha Patel¹ ; ⁹ ; Arif O. Khan¹ ; ² ; ⁹ ; Ahmad Mansour³ ; Jawahir Y. Mohamed¹ ; Abdullah Al-Assiri⁴ ; Randa Haddad³ ; Xiaofei Jia⁵ ; Yong Xiong⁵ ; André ; Mé ; garbané ; ⁶ ; Elias I. Traboulsi⁷ ; Fowzan S. Alkuraya¹ ; ⁸ ; ^{falkuraya@kfshrc.edu.sa" class="auth_mail}
• 刊名：The American Journal of Human Genetics
• 出版年：1 May 2014
• 年：2014
• 卷：94
• 期：5
• 页码：755-759
• 全文大小：1629 K

文摘

We have previously described a syndrome characterized by facial dysmorphism, lens dislocation, anterior-segment abnormalities, and spontaneous filtering blebs (FDLAB, or Traboulsi syndrome). In view of the consanguineous nature of the affected families and the likely autosomal-recessive inheritance pattern of this syndrome, we undertook autozygosity mapping and whole-exome sequencing to identify ASPH as the disease locus, in which we identified two homozygous mutations. ASPH encodes aspartyl/asparaginyl 尾-hydroxylase (ASPH), which has been found to hydroxylate aspartic acid and asparagine residues on epidermal growth factor (EGF)-domain-containing proteins. The truncating and missense mutations we identified are predicted to severely impair the enzymatic function of ASPH, which suggests a possible link to other forms of ectopia lentis given that many of the genes implicated in this phenotype encode proteins that harbor EGF domains. Developmental analysis of Asph revealed an expression pattern consistent with the proposed link to the human syndrome. Indeed, Asph-knockout mice had a foreshortened snout, which corresponds to the facial abnormalities in individuals with Traboulsi syndrome. These data support a genetic basis for a syndromic form of ectopia lentis and the role of aspartyl hydroxylation in human development.