A rare SNP in pre-miR-34a is associated with increased levels of miR-34a in pancreatic beta cells

• Published in: Acta diabetologica Vol. 51; no. 2; pp. 325 - 329
• Main Authors: Locke, Jonathan M., Lango Allen, Hana, Harries, Lorna W.
• Format: Journal Article
• Language: English
• Published: Milan Springer Milan 01.04.2014; Springer Nature B.V
• Subjects: Alleles; Cellular biology; Diabetes; Diabetes Mellitus, Type 2 - genetics; Diabetes Mellitus, Type 2 - metabolism; Genetic Variation; HeLa Cells; Humans; Insulin - metabolism; Insulin Secretion; Insulin-Secreting Cells - metabolism; Internal Medicine; Medicine; Medicine & Public Health; Metabolic Diseases; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; Pancreas; Polymorphism; Polymorphism, Single Nucleotide; Real-Time Polymerase Chain Reaction; RNA - chemistry; RNA - genetics; Short Communication; Transfection; miRNA; Beta cell; Single nucleotide polymorphism
• ISSN: 0940-5429; 1432-5233
• DOI: 10.1007/s00592-013-0499-1

Changes in the levels of specific microRNAs (miRNAs) can reduce glucose-stimulated insulin secretion and increase beta-cell apoptosis, two causes of islet dysfunction and progression to type 2 diabetes. Studies have shown that single nucleotide polymorphisms (SNPs) within miRNA genes can affect their expression. We sought to determine whether miRNAs, with a known role in beta-cell function, possess SNPs within the pre-miRNA structure which can affect their expression. Using published literature and dbSNP, we aimed to identify miRNAs with a role in beta-cell function that also possess SNPs within the region encoding its pre-miRNA. Following transfection of plasmids, encoding the pre-miRNA and each allele of the SNP, miRNA expression was measured. Two rare SNPs located within the pre-miRNA structure of two miRNA genes important to beta-cell function (miR-34a and miR-96) were identified. Transfection of INS-1 and MIN6 cells with plasmids encoding pre-miR-34a and the minor allele of rs72631823 resulted in significantly ( p  < 0.05) higher miR-34a expression, compared to cells transfected with plasmids encoding the corresponding major allele. Similarly, higher levels were also observed upon transfection of HeLa cells. Transfection of MIN6 cells with plasmids encoding pre-miR-96 and each allele of rs41274239 resulted in no significant differences in miR-96 expression. A rare SNP in pre-miR-34a is associated with increased levels of mature miR-34a. Given that small changes in miR-34a levels have been shown to cause increased levels of beta-cell apoptosis this finding may be of interest to studies looking at determining the effect of rare variants on type 2 diabetes susceptibility.