Expression of a developmentally-regulated neuron-specific isoform of the neurofibromatosis 1 (NF1) gene

被引:38
作者
Geist, RT
Gutmann, DH
机构
[1] WASHINGTON UNIV,SCH MED,DEPT NEUROL,ST LOUIS,MO 63110
[2] WASHINGTON UNIV,SCH MED,DEPT PEDIAT,ST LOUIS,MO 63110
[3] WASHINGTON UNIV,SCH MED,DEPT GENET,ST LOUIS,MO 63110
关键词
neurofibromatosis 1 (NF1) gene; neurons; central nervous system; isoform; learning disabilities; tumor suppressor gene;
D O I
10.1016/0304-3940(96)12730-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurofibromatosis 1 (NF1) is a common autosomal dominant disorder in which affected individuals develop benign and malignant tumors as well as non-tumor-related abnormalities, such as seizures and learning disabilities. Here, we report an NF1 isoform arising from the alternative splicing of exon 9a with predominant central nervous system (CNS) expression. Exon 9a expression is enriched in neurons of the forebrain, specifically septum, striatum, cortex, hippocampus and olfactory bulb with significantly less expression in brainstem, cerebellum and spinal cord. This pattern of NF1 exon 9a expression correlates with the postnatal maturation of these neurons and suggests a role for NF1 in neuronal differentiation.
引用
收藏
页码:85 / 88
页数:4
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