Literature DB >> 20400928

Genotyping the BDNF rs6265 (val66met) polymorphism by one-step amplified refractory mutation system PCR.

Haroon I Sheikh1, Elizabeth P Hayden, Katie R Kryski, Heather J Smith, Shiva M Singh.   

Abstract

BACKGROUND: The brain derived neutrophic factor (BDNF), a 27 kD polypeptide, is one of the most widely expressed neurotrophins in the brain, regulating neural development and plasticity. The BDNF gene contains a functional single-nucleotide polymorphism (rs6265), which results in a valine to methionine substitution (val66met), leading to reduced mature BDNF expression. This polymorphism has been widely implicated in a host of psychiatric disorders and is a focus of many ongoing psychiatric genetic studies.
OBJECTIVE: To develop an efficient and rapid method to detect the val66met polymorphism in a one-step PCR reaction. METHOD AND
RESULTS: We have designed four PCR primers that amplify the BDNF gene region containing rs6265. The specificity of the four primers in a single PCR reaction amplifies two allele-specific amplicons (253 and 201 bp) and the entire region (401 bp) as an internal control, which are easily distinguished on a polyacrylamide gel. The effectiveness and efficiency of the results are validated by traditional NlaIII restriction enzyme digestion, sequencing of resulting bands and confirmation on 308 genomic DNA samples.
CONCLUSION: This new method describes a rapid, sensitive, cost effective and high throughput genotyping of the BDNF val66met polymorphism, ideal for large-scale genotyping studies.

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Year:  2010        PMID: 20400928      PMCID: PMC2950863          DOI: 10.1097/YPG.0b013e32833a2038

Source DB:  PubMed          Journal:  Psychiatr Genet        ISSN: 0955-8829            Impact factor:   2.458


  18 in total

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2.  Lack of association between the BDNF Val66Met polymorphism and Parkinson's disease in a Swedish population.

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3.  The Val66Met coding variant of the brain-derived neurotrophic factor (BDNF) gene does not contribute toward variation in the personality trait neuroticism.

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4.  Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression.

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5.  An efficient procedure for genotyping single nucleotide polymorphisms.

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6.  The brain-derived neurotrophic factor val66met polymorphism and variation in human cortical morphology.

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7.  The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function.

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Journal:  Mol Psychiatry       Date:  2009-01-20       Impact factor: 15.992

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3.  Development of a cost-efficient novel method for rapid, concurrent genotyping of five common single nucleotide polymorphisms of the brain derived neurotrophic factor (BDNF) gene by tetra-primer amplification refractory mutation system.

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4.  The BDNF gene val66met polymorphism and behavioral inhibition in early childhood.

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6.  Duration-dependent effects of the BDNF Val66Met polymorphism on anodal tDCS induced motor cortex plasticity in older adults: a group and individual perspective.

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7.  Interactive effects of the APOE and BDNF polymorphisms on functional brain connectivity: the Tasmanian Healthy Brain Project.

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8.  Genomics as a Clinical Decision Support Tool: Successful Proof of Concept for Improved ASD Outcomes.

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9.  Shame and Guilt-Proneness in Adolescents: Gene-Environment Interactions.

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10.  Delayed plastic responses to anodal tDCS in older adults.

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