Baala Lekbir, Briault Sylvain, Etchevers Heather C, Laumonnier Frédéric, Natiq Abdelhafid, Amiel Jeanne, Boddaert Nathalie, Picard Capucine, Sbiti Aziza, Asermouh Abdellah, Attié-Bitach Tania, Encha-Razavi Féréchté, Munnich Arnold, Sefiani Abdelaziz, Lyonnet Stanislas
Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Maroc.
Nat Genet. 2007 Apr;39(4):454-6. doi: 10.1038/ng1993. Epub 2007 Mar 11.
Neural progenitor proliferation and migration influence brain size during neurogenesis. We report an autosomal recessive microcephaly syndrome cosegregating with a homozygous balanced translocation between chromosomes 3p and 10q, and we show that a position effect at the breakpoint on chromosome 3 silences the eomesodermin transcript (EOMES), also known as T-box-brain2 (TBR2). Together with the expression pattern of EOMES in the developing human brain, our data suggest that EOMES is involved in neuronal division and/or migration. Thus, mutations in genes encoding not only mitotic and apoptotic proteins but also transcription factors may be responsible for malformative microcephaly syndromes.
神经祖细胞的增殖和迁移在神经发生过程中影响脑容量。我们报告了一种常染色体隐性小头畸形综合征,它与3号染色体短臂和10号染色体长臂之间的纯合平衡易位共分离,并且我们发现3号染色体断点处的位置效应使也被称为T-盒脑2(TBR2)的胚中胚层决定因子转录本(EOMES)沉默。结合EOMES在发育中的人类大脑中的表达模式,我们的数据表明EOMES参与神经元分裂和/或迁移。因此,不仅编码有丝分裂和凋亡蛋白的基因,而且编码转录因子的基因发生突变都可能导致畸形小头畸形综合征。