Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.

Abstract

BACKGROUND:

Autism (MIM209850) is a neurodevelopmental disorder characterized by a triad of impairments, namely impairment in social interaction, impaired communication skills, and restrictive and repetitive behavior. A number of family and twin studies have demonstrated that genetic factors play a pivotal role in the etiology of autistic disorder. Various reports of reduced levels of reelin protein in the brain and plasma in autistic patients highlighted the role of the reelin gene (RELN) in autism. There is no such published study on the South African (SA) population.

AIMS:

The aim of the present study was to find the genetic association of intronic rs736707 and exonic rs362691 (single-nucleotide polymorphisms [SNPs] of the RELN gene) with autism in a SA population.

METHODS:

Genomic DNA was isolated from cheek cell swabs from autistic (136) as well as control (208) subjects. The TaqMan(®) Real-Time polymerase chain reaction and genotyping assay was utilized to determine the genotypes.

RESULTS:

A significant association of SNP rs736707, but not for SNP rs362691, with autism in the SA population is observed.

CONCLUSION:

There might be a possible role of RELN in autism, especially for SA populations. The present study represents the first report on genetic association studies on the RELN gene in the SA population.

• Authors: Jyoti Rajan Sharma, Zainunisha Arieff, Hajirah Gameeldien, Muneera Davids, Mandeep Kaur, Lize van der Merwe
• Journal: Genetic testing and molecular biomarkers (Genet Test Mol Biomarkers) Vol. 17 Issue 2 Pg. 93-8 (Feb 2013) ISSN: 1945-0257 [Electronic] United States
• PMID: 23216241 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Cell Adhesion Molecules, Neuronal
• Extracellular Matrix Proteins
• Nerve Tissue Proteins
• Reelin Protein
• RELN protein, human
• Serine Endopeptidases

Topics

• Adolescent
• Autistic Disorder (genetics)
• Cell Adhesion Molecules, Neuronal (genetics)
• Child
• Exons (genetics)
• Extracellular Matrix Proteins (genetics)
• Female
• Gene Frequency
• Genetic Association Studies
• Genetic Predisposition to Disease
• Genotype
• Humans
• Introns (genetics)
• Male
• Nerve Tissue Proteins (genetics)
• Polymorphism, Single Nucleotide
• Real-Time Polymerase Chain Reaction
• Reelin Protein
• Serine Endopeptidases (genetics)
• South Africa