Cuadrado Ana, García-Fernández Luis F, Imai Takao, Okano Hideyuki, Muñoz Alberto
Instituto de Investigaciones Biomédicas Alberto Sols, Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid, Spain.
Mol Cell Neurosci. 2002 Jun;20(2):198-210. doi: 10.1006/mcne.2002.1131.
The tau gene encodes a microtubule-associated protein expressed by neuronal and glial cells. Abnormal deposits of Tau protein are characteristic of several neurodegenerative disorders. Additionally, mutations affecting tau pre-mRNA alternative splicing of exon 10 are associated with frontotemporal dementia and Parkinsonism linked to chromosome 17. In rodents, this process is developmentally regulated by thyroid hormone (T3) causing the predominance of exon 10-containing transcripts. Here we demonstrate that musashi-1 (msi-1) gene is induced by T3 during rat brain development and in N2a cells. T3 increases msi-1 mRNA level in an actinomycin D-sensitive, cycloheximide-resistant fashion without affecting its half-life, which suggests a transcriptional effect. Both ectopic Msi-1 expression and T3 treatment increased the proportion of exon 10-containing tau transcripts. Furthermore, antisense msi-1 expression inhibited T3 action. Our results show that msi-1 mediates the posttranscriptional regulation of tau expression by T3.
tau基因编码一种由神经元和神经胶质细胞表达的微管相关蛋白。Tau蛋白的异常沉积是几种神经退行性疾病的特征。此外,影响第10外显子tau前体mRNA可变剪接的突变与17号染色体相关的额颞叶痴呆和帕金森综合征有关。在啮齿动物中,这一过程受甲状腺激素(T3)的发育调控,导致含第10外显子的转录本占优势。在此我们证明,在大鼠脑发育过程中和N2a细胞中,musashi-1(msi-1)基因受T3诱导。T3以对放线菌素D敏感、对放线菌酮耐药的方式增加msi-1 mRNA水平,且不影响其半衰期,这提示存在转录效应。异位表达Msi-1和T3处理均增加了含第10外显子的tau转录本比例。此外,反义msi-1表达抑制了T3的作用。我们的结果表明,msi-1介导了T3对tau表达的转录后调控。