Institute of Life Science, College of Medicine, Swansea University, Swansea SA2 8PP, UK.
Brain. 2013 Feb;136(Pt 2):536-48. doi: 10.1093/brain/aws338. Epub 2013 Jan 29.
Polymicrogyria and lissencephaly are causally heterogeneous disorders of cortical brain development, with distinct neuropathological and neuroimaging patterns. They can be associated with additional structural cerebral anomalies, and recurrent phenotypic patterns have led to identification of recognizable syndromes. The lissencephalies are usually single-gene disorders affecting neuronal migration during cerebral cortical development. Polymicrogyria has been associated with genetic and environmental causes and is considered a malformation secondary to abnormal post-migrational development. However, the aetiology in many individuals with these cortical malformations is still unknown. During the past few years, mutations in a number of neuron-specific α- and β-tubulin genes have been identified in both lissencephaly and polymicrogyria, usually associated with additional cerebral anomalies including callosal hypoplasia or agenesis, abnormal basal ganglia and cerebellar hypoplasia. The tubulin proteins form heterodimers that incorporate into microtubules, cytoskeletal structures essential for cell motility and function. In this study, we sequenced the TUBB2B and TUBA1A coding regions in 47 patients with a diagnosis of polymicrogyria and five with an atypical lissencephaly on neuroimaging. We identified four β-tubulin and two α-tubulin mutations in patients with a spectrum of cortical and extra-cortical anomalies. Dysmorphic basal ganglia with an abnormal internal capsule were the most consistent feature. One of the patients with a TUBB2B mutation had a lissencephalic phenotype, similar to that previously associated with a TUBA1A mutation. The remainder had a polymicrogyria-like cortical dysplasia, but the grey matter malformation was not typical of that seen in 'classical' polymicrogyria. We propose that the cortical malformations associated with these genes represent a recognizable tubulinopathy-associated spectrum that ranges from lissencephalic to polymicrogyric cortical dysplasias, suggesting shared pathogenic mechanisms in terms of microtubular function and interaction with microtubule-associated proteins.
脑回小且脑沟多和无脑回是皮质脑发育障碍的两种因果异质性疾病,具有不同的神经病理学和神经影像学模式。它们可能与其他结构性脑异常相关联,并且反复出现的表型模式导致了可识别的综合征的出现。无脑回通常是单基因疾病,影响皮质发育过程中的神经元迁移。脑回小且脑沟多与遗传和环境因素有关,被认为是由于异常的迁移后发育引起的畸形。然而,许多患有这些皮质畸形的个体的病因仍然未知。在过去的几年中,在无脑回和脑回小且脑沟多中已经鉴定出许多神经元特异性α-和β-微管蛋白基因的突变,通常与包括胼胝体发育不全或缺失、基底节和小脑发育不全在内的其他脑异常相关联。微管蛋白形成异二聚体,并入微管,这是细胞运动和功能所必需的细胞骨架结构。在这项研究中,我们对 47 名诊断为脑回小且脑沟多和 5 名神经影像学表现为非典型无脑回的患者的 TUBB2B 和 TUBA1A 编码区进行了测序。我们在具有皮质和皮质下异常的患者中发现了四个β-微管蛋白和两个α-微管蛋白突变。异常的内囊使形态异常的基底节是最一致的特征。一名具有 TUBB2B 突变的患者具有无脑回表型,类似于先前与 TUBA1A 突变相关的表型。其余患者具有类似于脑回小且脑沟多的皮质发育不良,但灰质畸形与“经典”脑回小且脑沟多所见的不同。我们提出,与这些基因相关的皮质畸形代表一种可识别的微管蛋白病相关谱,范围从无脑回到脑回小且脑沟多的皮质发育不良,表明在微管功能和与微管相关蛋白的相互作用方面具有共同的发病机制。