Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
Université de Paris, NeuroDiderot, UMR 1141, INSERM, Paris, France.
J Hum Genet. 2022 Mar;67(3):127-132. doi: 10.1038/s10038-021-00945-7. Epub 2021 Sep 10.
Mutations in MLC1 cause megalencephalic leukoencephalopathy with subcortical cysts (MLC), a rare form of leukodystrophy characterized by macrocephaly, epilepsy, spasticity, and slow mental deterioration. Genetic studies of MLC are lacking from many parts of the world, especially in Sub-Saharan Africa. Genomic DNA was extracted for 67 leukodystrophic patients from 43 Sudanese families. Mutations were screened using the NGS panel testing 139 leukodystrophies and leukoencephalopathies causing genes (NextSeq500 Illumina). Five homozygous MLC1 variants were discovered in seven patients from five distinct families, including three consanguineous families from the same region of Sudan. Three variants were missense (c.971 T > G, p.Ile324Ser; c.344 T > C, p.Phe115Ser; and c.881 C > T, p.Pro294Leu), one duplication (c.831_838dupATATCTGT, p.Ser280Tyrfs*8), and one synonymous/splicing-site mutation (c.762 C > T, p.Ser254). The segregation pattern was consistent with autosomal recessive inheritance. The clinical presentation and brain MRI of the seven affected patients were consistent with the diagnosis of MLC1. Due to the high frequency of distinct MLC1 mutations found in our leukodystrophic Sudanese families, we analyzed the coding sequence of MLC1 gene in 124 individuals from the Sudanese genome project in comparison with the 1000-genome project. We found that Sudan has the highest proportion of deleterious variants in MLC1 gene compared with other populations from the 1000-genome project.
MLC1 基因突变导致巨脑性脑白质营养不良伴皮质下囊肿(MLC),这是一种罕见的脑白质营养不良,其特征为大头畸形、癫痫、痉挛和智力逐渐下降。世界上许多地区,特别是撒哈拉以南非洲地区,缺乏对 MLC 的遗传研究。从 43 个苏丹家庭的 67 名脑白质营养不良患者中提取基因组 DNA。使用 NGS 面板测试 139 种脑白质营养不良和脑白质病致病基因(Illumina NextSeq500)对突变进行筛选。在来自五个不同家庭的七名患者中发现了五个纯合 MLC1 变体,包括来自苏丹同一地区的三个近亲家庭。三个变体是错义突变(c.971 T > G,p.Ile324Ser;c.344 T > C,p.Phe115Ser;和 c.881 C > T,p.Pro294Leu),一个重复(c.831_838dupATATCTGT,p.Ser280Tyrfs*8)和一个同义/剪接位点突变(c.762 C > T,p.Ser254)。遗传模式与常染色体隐性遗传一致。七名受影响患者的临床表现和脑部 MRI 与 MLC1 的诊断一致。由于我们在苏丹脑白质营养不良家庭中发现了高度独特的 MLC1 突变,因此我们分析了苏丹基因组计划中的 124 名个体与 1000 基因组计划中的 MLC1 基因编码序列。我们发现,与 1000 基因组计划中的其他人群相比,苏丹 MLC1 基因的有害变异比例最高。