Abstract
With an ever-increasing resource of validated single-nucleotide polymorphisms (SNPs), the limiting factors in genome-wide association analysis have become genotyping capacity and the availability of DNA. We provide a proof of concept of the use of pooled DNA as a means of efficiently screening SNPs and prioritizing them for further study. This approach reduces the final number of SNPs that undergo full, sample-by-sample genotyping as well as the quantity of DNA used overall. We have examined 15 SNPs in the cholesteryl ester transfer protein (CETP) gene, a gene previously demonstrated to be associated with serum high-density lipoprotein cholesterol levels. The SNPs were amplified in two pools of DNA derived from groups of individuals with extremely high and extremely low serum high-density lipoprotein cholesterol levels, respectively. P values <0.05 were obtained for 14 SNPs, supporting the described association. Genotyping of the individual samples showed that the average margin of error in frequency estimate was approximately 4% when pools were used. These findings clearly demonstrate the potential of pooling techniques and their associated technologies as an initial screen in the search for genetic associations.
MeSH Terms
Adolescent
Adult
Aged
Alleles
Carrier Proteins/genetics
Cholesterol Ester Transfer Proteins
Cholesterol, HDL/blood
Female
Gene Pool
Glycoproteins
Haplotypes
Humans
Middle Aged
Polymorphism, Single Nucleotide
Chemicals
CETP protein, human
Carrier Proteins
Cholesterol Ester Transfer Proteins
Cholesterol, HDL
Glycoproteins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Bansal Aruna
SEQUENOM-Gemini Ltd., 162 Cambridge Science Park, Milton Road, Cambridge, CB4 0GH England.
van den Boom Dirk
Kammerer Stefan
Honisch Christiane
Adam Gail
Cantor Charles R
Kleyn Patrick
Braun Andi
References (23)
23 references, click to expand
-
Heterogeneity at the CETP gene locus. Influence on plasma CETP concentrations and HDL cholesterol levels.
Arterioscler Thromb Vasc Biol. 1997 Mar;17(3):560-8
PMID: 9102177
-
The future of genetic studies of complex human diseases.
Science. 1996 Sep 13;273(5281):1516-7
PMID: 8801636
-
Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes.
Genome Res. 1998 Feb;8(2):111-23
PMID: 9477339
-
Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase.
Am J Hum Genet. 1998 Aug;63(2):595-612
PMID: 9683608
-
The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling.
Genome Res. 1998 Dec;8(12):1273-88
PMID: 9872982
-
Prospects for whole-genome linkage disequilibrium mapping of common disease genes.
Nat Genet. 1999 Jun;22(2):139-44
PMID: 10369254
-
Linkage disequilibrium in the human genome.
Nature. 2001 May 10;411(6834):199-204
PMID: 11346797
-
Genetic epidemiology of single-nucleotide polymorphisms.
Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):15173-7
PMID: 10611357
-
Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populations.
Am J Hum Genet. 2000 Jan;66(1):216-34
PMID: 10631153
-
New functional promoter polymorphism, CETP/-629, in cholesteryl ester transfer protein (CETP) gene related to CETP mass and high density lipoprotein cholesterol levels: role of Sp1/Sp3 in transcriptional regulation.
Arterioscler Thromb Vasc Biol. 2000 Feb;20(2):507-15
PMID: 10669650
-
Extensive association analysis between the CETP gene and coronary heart disease phenotypes reveals several putative functional polymorphisms and gene-environment interaction.
Genet Epidemiol. 2000 Jul;19(1):64-80
PMID: 10861897
-
Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations.
Am J Hum Genet. 2000 Jun;66(6):1882-99
PMID: 10788337
-
Extent and distribution of linkage disequilibrium in three genomic regions.
Am J Hum Genet. 2001 Jan;68(1):191-197
PMID: 11083947
-
High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):581-4
PMID: 11136232
-
Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia.
Atherosclerosis. 1985 Dec;58(1-3):175-86
PMID: 3937535
-
Rate of cholesteryl ester transfer between high and low density lipoproteins in human serum and a case with decreased transfer rate in association with hyperalphalipoproteinemia.
J Biochem. 1985 Dec;98(6):1499-508
PMID: 3867663
-
Cloning and sequencing of human cholesteryl ester transfer protein cDNA.
Nature. 1987 Jun 18-24;327(6123):632-4
PMID: 3600759
-
DNA polymorphism at the locus for human cholesteryl ester transfer protein (CETP) is associated with high density lipoprotein cholesterol and apolipoprotein levels.
Clin Genet. 1989 Jan;35(1):49-56
PMID: 2564326
-
Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome.
Genomics. 1990 Mar;6(3):575-7
PMID: 2184120
-
Polymorphisms in the gene coding for cholesteryl ester transfer protein are related to plasma high-density lipoprotein cholesterol and transfer protein activity.
Clin Sci (Lond). 1990 Dec;79(6):575-81
PMID: 1980239
-
An E-M algorithm and testing strategy for multiple-locus haplotypes.
Am J Hum Genet. 1995 Mar;56(3):799-810
PMID: 7887436
-
Direct measurement of high-density lipoprotein cholesterol in serum with polyethylene glycol-modified enzymes and sulfated alpha-cyclodextrin.
Clin Chem. 1995 May;41(5):717-23
PMID: 7729051
-
Association mapping of disease loci, by use of a pooled DNA genomic screen.
Am J Hum Genet. 1997 Sep;61(3):734-47
PMID: 9326338