| Literature DB >> 26212654 |
Yuanyuan Zong1, Pin Yu2, Hongxia Cheng1, Hailin Wang2, Xiaoying Wang2, Chunlian Liang2, Hua Zhu2, Yejun Qin3, Chuan Qin4.
Abstract
The microRNA-29 family (miRNA-29s) has three mature members, miR-29a, miR-29b and miR-29c, which have been implicated in the regulation of the pathogenesis of Alzheimer's disease (AD). The miR-29 family members exhibit differential regulation in various diseases and different subcellular distribution. In the present study, we initially investigated differential expression of miR-29c in the hippocampus and the frontal cortex of the young APPswe/PSΔE9 mouse brain, accompanied by inverse expression of neurone navigator 3 (NAV3), a regulator of axon guidance. We observed that miR-29c directly mediated downregulation of NAV3 protein expression in vitro. The mouse NAV3 mRNA has a functional miR-29c binding site in the 3' UTR, which localized in the position between 830-836 bp of 3'UTR region, slightly different from human NAV3 mRNA binding site. These observations suggest that miR-29c may be involved in neurodegenerative processes by regulating NAV3 expression in the young AD mouse.Entities:
Keywords: APPswe/PSΔE9 mice; Alzheimer׳s disease; NAV3 protein; miR-29c; microRNAs
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Year: 2015 PMID: 26212654 DOI: 10.1016/j.brainres.2015.07.022
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252