Association of the GNAS locus with severe malaria

Sarah Auburn1, Mahamadou Diakite, Andrew E Fry

  • 1Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Oxford, OX3 7BN, UK. sa3@sanger.ac.uk

Human Genetics
|October 28, 2008
PubMed

Insights

Genetic variations in the GNAS gene, encoding the stimulatory G protein alpha subunit (G-alpha-s), are associated with severe malaria risk. This suggests G-alpha-s influences parasite invasion and disease susceptibility.

Area of Science:

  • Genetics
  • Infectious Diseases
  • Molecular Biology

Background:

  • Functional studies show the stimulatory G protein alpha subunit (G-alpha-s) interacts with malaria parasites at the cellular level.
  • Blocking G-alpha-s signal transduction in erythrocytes reduces Plasmodium falciparum invasion.

Purpose of the Study:

  • To investigate the association between GNAS gene polymorphisms and severe malaria.
  • To determine if G-alpha-s signaling impacts malaria disease susceptibility at a population level.

Main Methods:

  • A large multi-center study including family and case-control cohorts from The Gambia, Kenya, Malawi, and Ghana.
  • Meta-analysis of seven studies with approximately 4,000 cases and 4,000 controls.
  • Investigation of 12 single nucleotide polymorphisms (SNPs) within the GNAS gene region.

Main Results:

  • Four out of 12 investigated SNPs showed significant association with severe malaria (P < 0.05).
  • The strongest single-locus association indicated an odds ratio of 1.13 (P = 0.001).
  • Significant associations were observed for haplotypes constructed from loci at the 5-prime end of the GNAS gene.

Conclusions:

  • Genetic variations in GNAS are linked to severe malaria susceptibility.
  • The findings support the role of G-alpha-s in erythrocyte invasion and its influence on individual disease risk.

Related Concept Videos

Malaria01:29

Malaria

Malaria pathogenesis in humans reflects a delicate interplay between parasite biology and host response. Clinical illness reflects a host’s immune response to the parasite’s asexual replication cycle, which is often asymptomatic in individuals with partial immunity. From the parasite's perspective, transmission between mosquito and human with minimal host pathology is evolutionarily advantageous. Among the six Plasmodium species infecting humans, P. falciparum and P. vivax dominate in global...
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
Symbiosis00:58

Symbiosis

Symbiotic relationships are long-term, close interactions between individuals of different species that affect the distribution and abundance of those species. When a relationship is beneficial to both species, this is called mutualism. When the relationship is beneficial to one species but neither beneficial nor harmful to the other species, this is called commensalism. When one organism is harmed to benefit another, the relationship is known as parasitism. These types of relationships often...
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...