| Sumario: | 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. A
|
|---|
