Human Lung Project: Evaluating Variance of Gene Expression in the Human Lung

Nondiseased tissue is an important reference for microarray studies of pulmonary disease. We obtained 23 single lungs from multiorgan donors at time of procurement. Donors varied in age, sex, smoking history, and ethnicity. Lungs were dissected into upper and lower lobe peripheral sections for RNA e...

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Veröffentlicht in:American journal of respiratory cell and molecular biology 2006-07, Vol.35 (1), p.65-71
Hauptverfasser: Gruber, Michael P, Coldren, Christopher D, Woolum, Malcolm D, Cosgrove, Gregory P, Zeng, Chan, Baron, Anna E, Moore, Mark D, Cool, Carlyne D, Worthen, G. Scott, Brown, Kevin K, Geraci, Mark W
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Sprache:eng
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Zusammenfassung:Nondiseased tissue is an important reference for microarray studies of pulmonary disease. We obtained 23 single lungs from multiorgan donors at time of procurement. Donors varied in age, sex, smoking history, and ethnicity. Lungs were dissected into upper and lower lobe peripheral sections for RNA extraction. Microarray analysis was performed using Affymetrix Hu-133 Plus 2.0 arrays. We observed that the relative variability of gene expression increased rapidly from technical (lowest), to regional, to population (highest). In addition, age and sex have measurable effects on gene expression. Gene expression variability is heterogeneously distributed among biologic categories. We conclude that gene expression variability is greater between individuals than within individuals and that population variability is the most important factor in the study design of microarray experiments of the human lung. Classes of genes with high population variability are biologically important and provide a novel perspective into lung physiology and pathobiology. Our study represents the first comprehensive analysis of nondiseased lung tissue. The generation of this robust dataset has important implications for the design and implementation of future comparative expression analysis with pulmonary disease states.
ISSN:1044-1549
1535-4989
DOI:10.1165/rcmb.2004-0261OC