Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
J Med Genet. 2011 Sep;48(9):597-601. doi: 10.1136/jmedgenet-2011-100306.
Knobloch syndrome (KS) is a developmental disorder characterised by occipital skull defect, high myopia, and vitreo-retinal degeneration. Although genetic heterogeneity has been suspected, COL18A1 is the only known KS disease gene to date.
To identify a novel genetic cause of KS in a cohort of Saudi KS patients enrolled in this study.
When COL18A1 mutation was excluded, autozygosity mapping was combined with exome sequencing.
In one patient with first cousin parents, COL18A1 was excluded by both linkage and direct sequencing. By filtering variants generated on exome sequencing using runs of autozygosity in this simplex case, the study identified ADAMTS18 as the only gene carrying a homozygous protein altering mutation. It was also shown that Adamts18 is expressed in the lens and retina in the developing murine eye.
The power of combining exome and autozygome analysis in the study of genetics of autosomal recessive disorders, even in simplex cases, has been demonstrated.
诺布洛克综合征(KS)是一种以枕骨颅骨缺损、高度近视和玻璃视网膜变性为特征的发育障碍。尽管已经怀疑存在遗传异质性,但 COL18A1 是迄今为止唯一已知的 KS 疾病基因。
在本研究纳入的一组沙特 KS 患者中,确定一种新的 KS 遗传病因。
当排除 COL18A1 突变时,采用自交系作图与外显子组测序相结合的方法。
在一位一级表亲父母的患者中,COL18A1 既通过连锁又通过直接测序被排除。通过在这个单体型病例中使用自交系中的串联重复来筛选外显子组测序产生的变异,研究发现 ADAMTS18 是唯一携带纯合蛋白改变突变的基因。还表明 Adamts18 在发育中的鼠眼晶状体和视网膜中有表达。
即使在单体型病例中,外显子组和自交系分析相结合在常染色体隐性遗传疾病的遗传学研究中的作用已经得到了证明。