Cited by 28Genetic Associations and EpidemiologyMicroRNA in disease regulationMolecular Biology Techniques and Applications

Analysis of a polymorphic microRNA target site in the purinergic receptor P2RX7 gene

Rahman, Omar Abdul, Sasvari‐Szekely, Maria, Szekely, Anna, Faludi, Gabor, Guttman, Andras, Nemoda, Zsofia·2010·ELECTROPHORESIS

Abstract

The recent discovery of post‐transcriptional regulation by microRNAs (miRNAs) drew our attention to SNPs of putative miRNA target sites in candidate genes of depression‐related psychiatric disorders. The P2RX7 (purinergic receptor P2X, ligand‐gated ion channel, 7) gene has been suggested as a candidate for major depressive and bipolar disorder, because of repeated associations with the rs2230912 (Gln460Arg) polymorphism. As this polymorphism is located at the end of the coding region, we considered a possible linkage with SNP(s) in putative miRNA target sites of the 3′ untranslated region. Based on our in silico search, the rs1653625 fulfilled this criterion. This SNP, however, is surrounded with polycytosine and polyadenine tracts, which hindered its analysis until now. In this study, we describe a readily applicable genotyping method for rs1653625 by applying a primer that introduces mismatched nucleotides to create a restriction enzyme cleavage site. The resulting allele‐specific products with 19 base pair difference were separated by both traditional horizontal agarose gel electrophoresis and multicapillary gel electrophoresis. The developed genotyping method was applied in our depression‐related association study.

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Crossref · 10.1002/elps.200900664

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  • A handful of studies have identified depression risk variants in precursor miRNA encoding genes, miRNA target genes, or genes involved in miRNA processing.

    “A handful of studies have also identified depression risk variants in precursor miRNA encoding genes, 44 , 45 variants located in or near miRNA target genes 46 , 47 or variants located in genes involved in miRNA processing.”

    From Epigenetics and depression (2019) · cites this paper as [46]

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Authors
Rahman, O. A., Sasvari‐Szekely, M., Szekely, A., Faludi, G., Guttman, A., & Nemoda, Z.
Affiliations
Semmelweis University (HU)
Venue
ELECTROPHORESIS
Publisher
Wiley
Published
2010-05-26
Volume
31
Issue
11
Pages
1790-1795
ISSN
  • 0173-0835 (ISSN-L)
  • 1522-2683
OpenAlex
W1935099637
Cited by
28
References
2
Citations by year
2025: 1 · 2022: 1 · 2021: 1 · 2020: 1 · 2019: 3 · 2017: 2 · 2016: 2 · 2015: 1 · 2014: 8 · 2013: 5
FWCI
1.26
Type
journal article
Language
en
Open access
closed
Locations
  • Electrophoresis (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Molecular Biology Techniques and Applications
Keywords
P2X7 receptor, microRNA binding sites, 3' untranslated region, single nucleotide polymorphisms, restriction enzyme cleavage sites, major depressive disorder, bipolar disorder, post-transcriptional regulation
MeSH terms
Base Sequence, Cloning, Molecular, Computer Simulation, Depression, DNA Mutational Analysis, Genotype, Humans, Molecular Sequence Data, Polymorphism, Restriction Fragment Length, Reproducibility of Results, Linkage Disequilibrium, Chi-Square Distribution, Polymerase Chain Reaction, Receptors, Purinergic P2, Electrophoresis, Capillary, Base Pair Mismatch, Polymorphism, Single Nucleotide, MicroRNAs, Receptors, Purinergic P2X7

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