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Integrating Genomic Analysis with the Genetic Basis of Gene Expression: Preliminary Evidence of the Identification of Causal Genes for Cardiovascular and Metabolic Traits Related to Nutrition in Mexicans
Author(s) -
Raúl A. Bastarrachea,
Esther C. Gallegos-Cabriales,
Edna J. NavaGonzález,
Karin Haack,
V. Saroja Voruganti,
Jac Charlesworth,
Hugo LaviadaMolina,
Rosa A. Veloz-Garza,
Velia Margarita Cárdenas-Villarreal,
Salvador Bruno Valdovinos-Chávez,
Patricia Isolina del Socorro Gómez-Aguilar,
Guillermo Meléndez,
Juan Carlos López-Alvarenga,
Harald H.H. Göring,
Shelley A. Cole,
John Blangero,
Anthony G. Comuzzie,
Jack W. Kent
Publication year - 2012
Publication title -
advances in nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.362
H-Index - 90
eISSN - 2156-5376
pISSN - 2161-8313
DOI - 10.3945/an.112.001925
Subject(s) - biology , expression quantitative trait loci , transcriptome , gene , quantitative trait locus , phenotype , genetics , gene expression , gene expression profiling , computational biology , genomics , functional genomics , genotype , single nucleotide polymorphism , genome
Whole-transcriptome expression profiling provides novel phenotypes for analysis of complex traits. Gene expression measurements reflect quantitative variation in transcript-specific messenger RNA levels and represent phenotypes lying close to the action of genes. Understanding the genetic basis of gene expression will provide insight into the processes that connect genotype to clinically significant traits representing a central tenet of system biology. Synchronous in vivo expression profiles of lymphocytes, muscle, and subcutaneous fat were obtained from healthy Mexican men. Most genes were expressed at detectable levels in multiple tissues, and RNA levels were correlated between tissue types. A subset of transcripts with high reliability of expression across tissues (estimated by intraclass correlation coefficients) was enriched for cis-regulated genes, suggesting that proximal sequence variants may influence expression similarly in different cellular environments. This integrative global gene expression profiling approach is proving extremely useful for identifying genes and pathways that contribute to complex clinical traits. Clearly, the coincidence of clinical trait quantitative trait loci and expression quantitative trait loci can help in the prioritization of positional candidate genes. Such data will be crucial for the formal integration of positional and transcriptomic information characterized as genetical genomics.

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