• Journal Article

Identification of quantitative trait loci underlying proteome variation in human lymphoblastoid cells

Citation

Garge, N., Pan, H., Rowland, M. D., Cargile, B., Zhang, X., Cooley, P., ... Bunger, M. (2010). Identification of quantitative trait loci underlying proteome variation in human lymphoblastoid cells. Molecular & Cellular Proteomics, 9(7), 1383-1399. DOI: 10.1074/mcp.M900378-MCP200

Abstract

Population-based variability in protein expression patterns, especially in humans, is often observed but poorly understood. Moreover, very little is known about how inter-individual genetic variation contributes to protein expression patterns. To begin to address this, we describe elements of technical and biological variation contributing to expression of 544 proteins in a population of 24 individual human lymphoblastoid cell lines (LCLs) that have been extensively genotyped as part of the International HapMap Project. We determined that expression levels of 10% of the proteins were tightly correlated to cell-doubling rates. Using the publicly available genotypes for these LCLs, we applied a genetic association approach to identify quantitative trait loci associated with protein expression variation (peQTL). Results identified 24 protein forms corresponding to 15 proteins for which genetic elements were responsible for > 50% of the expression variation. The genetic variation associated with protein expression levels were located in cis with the gene coding for the protein’s transcript for 19 of these protein forms. Four of the genetic elements identified were coding non-synonymous single nucleotide polymorphisms (NS-SNPs) that resulted in migration pattern changes in the two-dimensional (2D) gel. This is the first description of large-scale proteomic analysis demonstrating the direct relationship between genome and proteome variation in human cells.