Evidence map›Paper›PMID 40646112›Full record

ArticleScientific reports2025

Improved approaches to genotyping MAOA-uVNTR polymorphisms with novel allele discovery.

Areerat Hnoonual, Potchanapond Graidist, Pornprot Limprasert

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Areerat HnoonualDepartment of Pathology, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
Potchanapond GraidistDepartment of Biomedical Sciences and Biomedical Engineering, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
Pornprot LimprasertDepartment of Pathology, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand. pornprot.l@psu.ac.th.

Funding

Faculty of Medicine, Prince of Songkla University No. 55-235-05-1-3
6 · The paper itself

Abstract

A functional polymorphic 30 bp tandem repeat in the upstream regulatory region of the MAOA gene (MAOA-uVNTR) is extensively studied in relation to behavioral and neurobiological traits. The discrepancies of MAOA-uVNTR frequencies may be due to differences in racial and ethnic enrollment and methodologies for detecting alleles. This study aimed to enhance genotyping accuracy of MAOA-uVNTR polymorphisms by comparing conventional PCR and fluorescent PCR methods. Concordance analysis revealed 97.3% agreement (178/183). Discordant results were confirmed by Sanger sequencing, which validated the fluorescent PCR results but identified inaccuracies in conventional PCR findings. The study identified five common alleles (2.5R, 3.5R, 4.5R, 5.5R) and discovered a novel allele, 3.3R, through fluorescent PCR. Functional analysis using luciferase reporter vectors demonstrated 1.5-2.0 times higher transcriptional activity for the 3.3R and 4.5R alleles compared with 3.5R and 5.5R alleles in LA-N-5 and SK-N-SH cell lines. This emphasizes fluorescent PCR as a superior method for identifying MAOA-uVNTR polymorphisms, including novel alleles, with higher resolution and accuracy than conventional PCR. The approach eliminates the need for confirmatory sequencing of known alleles, providing time and cost efficiency. These findings support the use of fluorescent PCR as the preferred technique for accurate genotyping of MAOA-uVNTR and other tandem repeats.

Indexed as

AllelesGenotyping TechniquesMonoamine OxidasePolymorphism, GeneticTandem Repeat SequencesGenotypeHumansPolymerase Chain ReactionMonoamine Oxidasemonoamine oxidase A, humanMAOAMonoamine oxidase APolymorphismTandem repeatsVNTR

Identifiers

PMID40646112
PMCPMC12254254

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.