Institute of Medical Genetics, Charité, University Medicine of Berlin, Berlin, Germany.
Hum Mutat. 2010 Nov;31(11):E1851-60. doi: 10.1002/humu.21362.
Mental retardation affects 2-3% of the population and shows a high heritability.Neurodevelopmental disorders that include pronounced impairment in language and speech skills occur less frequently. For most cases, the molecular basis of mental retardation with or without speech and language disorder is unknown due to the heterogeneity of underlying genetic factors.We have used molecular karyotyping on 1523 patients with mental retardation to detect copy number variations (CNVs) including deletions or duplications. These studies revealed three heterozygous overlapping deletions solely affecting the forkhead box P1 (FOXP1) gene. All three patients had moderate mental retardation and significant language and speech deficits. Since our results are consistent with a de novo occurrence of these deletions, we considered them as causal although we detected a single large deletion including FOXP1 and additional genes in 4104 ancestrally matched controls. These findings are of interest with regard to the structural and functional relationship between FOXP1 and FOXP2. Mutations in FOXP2 have been previously related to monogenic cases of developmental verbal dyspraxia. Both FOXP1 and FOXP2 are expressed in songbird and human brain regions that are important for the developmental processes that culminate in speech and language.
精神发育迟滞影响 2-3%的人口,具有较高的遗传性。神经发育障碍包括语言和言语技能明显受损的情况较少发生。对于大多数病例,由于潜在遗传因素的异质性,伴有或不伴有言语和语言障碍的精神发育迟滞的分子基础尚不清楚。我们使用分子核型分析对 1523 名精神发育迟滞患者进行了检测,以发现包括缺失或重复在内的拷贝数变异(CNVs)。这些研究揭示了三个纯合重叠缺失,仅影响叉头框 P1(FOXP1)基因。所有三名患者均有中度精神发育迟滞和明显的语言和言语障碍。由于我们的结果与这些缺失的新生发生一致,因此尽管我们在 4104 名祖先匹配的对照中检测到包括 FOXP1 和其他基因在内的单个大型缺失,但我们认为它们是因果关系。这些发现与 FOXP1 和 FOXP2 之间的结构和功能关系有关。FOXP2 的突变以前与发育性言语运动障碍的单基因病例有关。FOXP1 和 FOXP2 均在鸣禽和人类大脑区域中表达,这些区域对导致言语和语言的发育过程很重要。