Pediatric Neurology Hopital Necker Enfants Malades, Université Paris Descartes, APHP, 149 rue de Sevres 75015 Paris, France.
Brain. 2013 Jan;136(Pt 1):223-44. doi: 10.1093/brain/aws323.
X-linked isolated lissencephaly sequence and subcortical band heterotopia are allelic human disorders associated with mutations of doublecortin (DCX), giving both familial and sporadic forms. DCX encodes a microtubule-associated protein involved in neuronal migration during brain development. Structural data show that mutations can fall either in surface residues, likely to impair partner interactions, or in buried residues, likely to impair protein stability. Despite the progress in understanding the molecular basis of these disorders, the prognosis value of the location and impact of individual DCX mutations has largely remained unclear. To clarify this point, we investigated a cohort of 180 patients who were referred with the agyria-pachygyria subcortical band heterotopia spectrum. DCX mutations were identified in 136 individuals. Analysis of the parents' DNA revealed the de novo occurrence of DCX mutations in 76 cases [62 of 70 females screened (88.5%) and 14 of 60 males screened (23%)], whereas in the remaining cases, mutations were inherited from asymptomatic (n = 14) or symptomatic mothers (n = 11). This represents 100% of families screened. Female patients with DCX mutation demonstrated three degrees of clinical-radiological severity: a severe form with a thick band (n = 54), a milder form (n = 24) with either an anterior thin or an intermediate thickness band and asymptomatic carrier females (n = 14) with normal magnetic resonance imaging results. A higher proportion of nonsense and frameshift mutations were identified in patients with de novo mutations. An analysis of predicted effects of missense mutations showed that those destabilizing the structure of the protein were often associated with more severe phenotypes. We identified several severe- and mild-effect mutations affecting surface residues and observed that the substituted amino acid is also critical in determining severity. Recurrent mutations representing 34.5% of all DCX mutations often lead to similar phenotypes, for example, either severe in sporadic subcortical band heterotopia owing to Arg186 mutations or milder in familial cases owing to Arg196 mutations. Taken as a whole, these observations demonstrate that DCX-related disorders are clinically heterogeneous, with severe sporadic and milder familial subcortical band heterotopia, each associated with specific DCX mutations. There is a clear influence of the individual mutated residue and the substituted amino acid in determining phenotype severity.
X 连锁单纯性脑裂畸形序列和皮质下带状异位是与双皮质素 (DCX) 突变相关的人类遗传性疾病,具有家族性和散发性两种形式。DCX 编码一种微管相关蛋白,参与脑发育过程中的神经元迁移。结构数据表明,突变可发生在表面残基上,可能会损害相互作用的伴侣,也可发生在埋藏残基上,可能会损害蛋白质稳定性。尽管人们对这些疾病的分子基础有了一定的了解,但 DCX 突变的位置和影响的预后价值在很大程度上仍不清楚。为了阐明这一点,我们研究了一个由 180 名患者组成的队列,这些患者被转诊为脑回发育不良-脑回发育不良的皮质下带状异位谱系。在 136 名个体中发现了 DCX 突变。对父母 DNA 的分析显示,在 76 例病例中发现了 DCX 突变的新生现象[70 例筛查女性中的 62 例(88.5%)和 60 例筛查男性中的 14 例(23%)],而在其余病例中,突变是从无症状的母亲(n = 14)或有症状的母亲(n = 11)遗传而来的。这代表了筛查的所有家庭。携带 DCX 突变的女性患者表现出三种临床-放射学严重程度:严重型(有厚带)(n = 54)、较轻型(n = 24),表现为前薄带或中间厚度带,无症状携带者(n = 14)的磁共振成像结果正常。在新生突变患者中发现了更高比例的无义和移码突变。对错义突变预测效应的分析表明,那些破坏蛋白质结构的突变往往与更严重的表型相关。我们鉴定了一些影响表面残基的严重和轻度效应突变,并观察到取代的氨基酸在确定严重程度方面也很关键。占所有 DCX 突变的 34.5%的反复突变通常导致类似的表型,例如,由于 Arg186 突变导致散发性皮质下带状异位的严重型,或由于 Arg196 突变导致家族性病例的较轻型。总的来说,这些观察结果表明,DCX 相关疾病在临床上是异质性的,包括严重的散发性和较轻微的家族性皮质下带状异位,每种疾病都与特定的 DCX 突变相关。个体突变残基和取代氨基酸在决定表型严重程度方面有明显的影响。