Alterations of the microRNA network cause neurodegenerative disease

被引:373
作者
Hebert, Sebastien S. [1 ,2 ]
De Strooper, Bart [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Ctr Human Genet, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven VIB, Dept Mol & Dev Genet, B-3000 Louvain, Belgium
关键词
ALZHEIMERS-DISEASE; PRECURSOR-PROTEIN; NEURONAL DIFFERENTIATION; LOCUS DUPLICATION; MIRNA EXPRESSION; GENE-EXPRESSION; BETA-SECRETASE; BINDING-SITE; RNA; BRAIN;
D O I
10.1016/j.tins.2008.12.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Brain development crucially depends on the integrity of microRNA (miRNA) pathways, which function at the post-transcriptional level as a rheostat of the transcriptome and proteome of the cell. miRNAs are also involved in many other, more specific, aspects of neuronal function such as neurite outgrowth and synapse formation. Complete loss of miRNA expression in the brain leads to neurodegeneration in several animal models. Evidence from patient material is emerging that miRNA dysregulation could, indeed, contribute to neurodegenerative disorders. The translation of proteins previously implicated in familial forms of disease seems to be under control of miRNAs, and changes in miRNAs might explain how these proteins become affected in sporadic neurodegenerative disease. Thus, miRNAs are moving rapidly center stage as key regulators of neuronal development and function in addition to important contributors to neurodegenerative disorder.
引用
收藏
页码:199 / 206
页数:8
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