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On the Integration of Alcohol‐Related Quantitative Trait Loci and Gene Expression Analyses
Author(s) -
Hitzemann Robert,
Reed Cheryl,
Malmanger Barry,
Lawler Maureen,
Hitzemann Barbara,
Cunningham Brendan,
McWeeney Shan,
Belknap John,
Harrington Christina,
Buck Kari,
Phillips Tamara,
Crabbe John
Publication year - 2004
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1097/01.alc.0000139827.86749.da
Subject(s) - quantitative trait locus , biology , genetics , gene , gene expression , trait , expression quantitative trait loci , phenotype , genotype , single nucleotide polymorphism , computer science , programming language
Background: Quantitative trait loci (QTLs) have been detected for a wide variety of ethanol‐related phenotypes, including acute and chronic ethanol withdrawal, acute locomotor activation, and ethanol preference. This study was undertaken to determine whether the process of moving from QTL to quantitative trait gene (QTG) could be accelerated by the integration of functional genomics (gene expression) into the analysis strategy. Methods: Six ethanol‐related QTLs, all detected in C57BL/6J and DBA/2J intercrosses were entered into the analysis. Each of the QTLs had been confirmed in independent genetic models at least once; the cumulative probabilities for QTL existence ranged from 10 −6 to 10 −15 . Brain gene expression data for the C57BL/6 and DBA/2 strains ( n = 6 per strain) and an F 2 intercross sample ( n = 56) derived from these strains were obtained by using the Affymetrix U74Av2 and 430A arrays; additional data with the U74Av2 array were available for the extended amygdala, dorsomedial striatum, and hippocampus. Low‐level analysis was performed by using multiple methods to determine the likelihood that a transcript was truly differentially expressed. For the 430A array data, the F 2 sample was used to determine which of the differentially expressed transcripts within the QTL intervals were cis ‐regulated and, thus, strong candidates for QTGs. Results: Within the 6 QTL intervals, 39 transcripts (430A array) were identified as being highly likely to be differentially expressed between the C57BL/6 and DBA/2 strains at a false discovery rate of 0.01 or better. Twenty‐eight of these transcripts showed significant (logarithm of odds ≥3.6) to highly significant (logarithm of odds >7) cis ‐regulation. The process correctly detected Mpdz (chromosome 4) as a candidate QTG for acute withdrawal. Conclusions: Although improvements are needed in the expression databases, the integration of QTL and gene expression analyses seems to have potential as a high‐throughput strategy for moving from QTL to QTG.