» Articles » PMID: 17206142

Common Genetic Variants Account for Differences in Gene Expression Among Ethnic Groups

Overview
Journal Nat Genet
Specialty Genetics
Date 2007 Jan 9
PMID 17206142
Citations 264
Authors
Affiliations
Soon will be listed here.
Abstract

Variation in DNA sequence contributes to individual differences in quantitative traits, but in humans the specific sequence variants are known for very few traits. We characterized variation in gene expression in cells from individuals belonging to three major population groups. This quantitative phenotype differs significantly between European-derived and Asian-derived populations for 1,097 of 4,197 genes tested. For the phenotypes with the strongest evidence of cis determinants, most of the variation is due to allele frequency differences at cis-linked regulators. The results show that specific genetic variation among populations contributes appreciably to differences in gene expression phenotypes. Populations differ in prevalence of many complex genetic diseases, such as diabetes and cardiovascular disease. As some of these are probably influenced by the level of gene expression, our results suggest that allele frequency differences at regulatory polymorphisms also account for some population differences in prevalence of complex diseases.

Citing Articles

MerQuaCo: a computational tool for quality control in image-based spatial transcriptomics.

Martin N, Olsen P, Quon J, Campos J, Cuevas N, Nagra J bioRxiv. 2024; .

PMID: 39677693 PMC: 11643037. DOI: 10.1101/2024.12.04.626766.


Heterogeneous genetic architectures of prostate cancer susceptibility in sub-Saharan Africa.

Janivara R, Chen W, Hazra U, Baichoo S, Agalliu I, Kachambwa P Nat Genet. 2024; 56(10):2093-2103.

PMID: 39358599 DOI: 10.1038/s41588-024-01931-3.


Risk factors associated with the Motoric Cognitive Risk syndrome: A meta-analysis of data from a cross-national study.

Jayakody O, Blumen H, Breslin M, Wang C, Verghese J J Am Geriatr Soc. 2024; 72(9):2656-2666.

PMID: 38872608 PMC: 11368625. DOI: 10.1111/jgs.19032.


Age and Sex-related Chromogranin A Gene Polymorphisms and its Association with Metabolic Syndrome Components.

Marjani A, Poursharifi N, Sajedi A, Tatari M J ASEAN Fed Endocr Soc. 2024; 39(1):45-52.

PMID: 38863909 PMC: 11163322. DOI: 10.15605/jafes.039.01.09.


Associations of the circulating levels of cytokines with the risk of myeloproliferative neoplasms: a bidirectional mendelian-randomization study.

Xiong H, Zhang H, Bai J, Li Y, Li L, Zhang L BMC Cancer. 2024; 24(1):531.

PMID: 38671390 PMC: 11046808. DOI: 10.1186/s12885-024-12301-x.


References
1.
Yan H, Yuan W, Velculescu V, Vogelstein B, Kinzler K . Allelic variation in human gene expression. Science. 2002; 297(5584):1143. DOI: 10.1126/science.1072545. View

2.
McEvoy B, Beleza S, Shriver M . The genetic architecture of normal variation in human pigmentation: an evolutionary perspective and model. Hum Mol Genet. 2006; 15 Spec No 2:R176-81. DOI: 10.1093/hmg/ddl217. View

3.
Cheung V, Conlin L, Weber T, Arcaro M, Jen K, Morley M . Natural variation in human gene expression assessed in lymphoblastoid cells. Nat Genet. 2003; 33(3):422-5. DOI: 10.1038/ng1094. View

4.
Schadt E, Monks S, Drake T, Lusis A, Che N, Colinayo V . Genetics of gene expression surveyed in maize, mouse and man. Nature. 2003; 422(6929):297-302. DOI: 10.1038/nature01434. View

5.
Pastinen T, Sladek R, Gurd S, Sammak A, Ge B, Lepage P . A survey of genetic and epigenetic variation affecting human gene expression. Physiol Genomics. 2003; 16(2):184-93. DOI: 10.1152/physiolgenomics.00163.2003. View