» Articles » PMID: 27328823

Genome-wide Identification of MicroRNA-related Variants Associated with Risk of Alzheimer's Disease

Overview
Journal Sci Rep
Specialty Science
Date 2016 Jun 23
PMID 27328823
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

MicroRNAs (miRNAs) serve as key post-transcriptional regulators of gene expression. Genetic variation in miRNAs and miRNA-binding sites may affect miRNA function and contribute to disease risk. Here, we investigated the extent to which variants within miRNA-related sequences could constitute a part of the functional variants involved in developing Alzheimer's disease (AD), using the largest available genome-wide association study of AD. First, among 237 variants in miRNAs, we found rs2291418 in the miR-1229 precursor to be significantly associated with AD (p-value = 6.8 × 10(-5), OR = 1.2). Our in-silico analysis and in-vitro miRNA expression experiments demonstrated that the variant's mutant allele enhances the production of miR-1229-3p. Next, we found miR-1229-3p target genes that are associated with AD and might mediate the miRNA function. We demonstrated that miR-1229-3p directly controls the expression of its top AD-associated target gene (SORL1) using luciferase reporter assays. Additionally, we showed that miR-1229-3p and SORL1 are both expressed in the human brain. Second, among 42,855 variants in miRNA-binding sites, we identified 10 variants (in the 3' UTR of 9 genes) that are significantly associated with AD, including rs6857 that increases the miR-320e-mediated regulation of PVRL2. Collectively, this study shows that miRNA-related variants are associated with AD and suggests miRNA-dependent regulation of several AD genes.

Citing Articles

Investigation of the role of miRNA variants in neurodegenerative brain diseases.

Frydas A, Cacace R, van der Zee J, Van Broeckhoven C, Wauters E Front Genet. 2025; 16:1506169.

PMID: 40078479 PMC: 11897046. DOI: 10.3389/fgene.2025.1506169.


Predicting functional UTR variants by integrating region-specific features.

Li G, Wu J, Wang X Brief Bioinform. 2024; 25(4).

PMID: 38783704 PMC: 11116830. DOI: 10.1093/bib/bbae248.


Phenome-wide association study on miRNA-related sequence variants: the UK Biobank.

Mustafa R, Ghanbari M, Karhunen V, Evangelou M, Dehghan A Hum Genomics. 2023; 17(1):104.

PMID: 37996941 PMC: 10668386. DOI: 10.1186/s40246-023-00553-w.


The role of microRNAs in neurobiology and pathophysiology of the hippocampus.

Rashidi S, Kalirad A, Rafie S, Behzad E, Dezfouli M Front Mol Neurosci. 2023; 16:1226413.

PMID: 37727513 PMC: 10506409. DOI: 10.3389/fnmol.2023.1226413.


In silico prioritisation of microRNA-associated common variants in multiple sclerosis.

Fashina I, McCoy C, Furney S Hum Genomics. 2023; 17(1):31.

PMID: 36991503 PMC: 10061723. DOI: 10.1186/s40246-023-00478-4.


References
1.
Naj A, Jun G, Beecham G, Wang L, Vardarajan B, Buros J . Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet. 2011; 43(5):436-41. PMC: 3090745. DOI: 10.1038/ng.801. View

2.
Heman-Ackah S, Hallegger M, Rao M, Wood M . RISC in PD: the impact of microRNAs in Parkinson's disease cellular and molecular pathogenesis. Front Mol Neurosci. 2013; 6:40. PMC: 3834244. DOI: 10.3389/fnmol.2013.00040. View

3.
Jeyaseelan K, Lim K, Armugam A . MicroRNA expression in the blood and brain of rats subjected to transient focal ischemia by middle cerebral artery occlusion. Stroke. 2008; 39(3):959-66. DOI: 10.1161/STROKEAHA.107.500736. View

4.
Grundberg E, Small K, Hedman A, Nica A, Buil A, Keildson S . Mapping cis- and trans-regulatory effects across multiple tissues in twins. Nat Genet. 2012; 44(10):1084-9. PMC: 3784328. DOI: 10.1038/ng.2394. View

5.
Tan L, Yu J, Tan L . Causes and Consequences of MicroRNA Dysregulation in Neurodegenerative Diseases. Mol Neurobiol. 2014; 51(3):1249-62. DOI: 10.1007/s12035-014-8803-9. View