小RNA
生物
淀粉样前体蛋白
基因表达调控
内生
基因
细胞生物学
基因表达
神经科学
阿尔茨海默病
疾病
遗传学
内科学
医学
内分泌学
作者
Sébastien S. Hébert,Katrien Horré,Laura Nicolaï,Bruno Bergmans,Aikaterini S. Papadopoulou,André Delacourte,Bart De Strooper
标识
DOI:10.1016/j.nbd.2008.11.009
摘要
Gene dosage effects of Amyloid precursor protein (APP) can cause familial AD. Recent evidence suggest that microRNA (miRNA) pathways, implicated in gene transcriptional control, could be involved in the development of sporadic Alzheimer's disease (AD). We therefore investigated whether miRNAs could participate in the regulation of APP gene expression. We show that miRNAs belonging to the miR-20a family (that is, miR-20a, miR-17-5p and miR-106b) could regulate APP expression in vitro and at the endogenous level in neuronal cell lines. A tight correlation between these miRNAs and APP was found during brain development and in differentiating neurons. We thus identify miRNAs as novel endogenous regulators of APP expression, suggesting that variations in miRNA expression could contribute to changes in APP expression in the brain during development and disease. This possibility is further corroborated by the observation that a statistically significant decrease in miR-106b expression was found in sporadic AD patients.
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