Literature DB >> 9880656

Genes on mouse chromosomes 2 and 9 determine variation in ethanol consumption.

T J Phillips1, J K Belknap, K J Buck, C L Cunningham.   

Abstract

Quantitative trait locus (QTL) mapping efforts in alcohol (ethanol) research are beginning to generate promising data that may ultimately lead to the identification of genes influencing alcohol addiction. Rodents have been extensively utilized to study ethanol's rewarding and aversive effects, and to demonstrate the existence of genetic influences on traits such as free-choice ethanol-consumption, ethanol-conditioned place preference and ethanol-conditioned taste aversion. The purpose of the current investigation was to verify or eliminate from further consideration putative QTLs for free-choice ethanol consumption originally identified in BXD Recombinant Inbred (RI) strains and other informative genetic crosses. B6D2F2 mice were utilized in a verification testing strategy to evaluate the viability of putative ethanol consumption QTLs. When data were combined from BXD RI, B6D2F2 and short-term selected line (STSL) mapping studies, verification was obtained for two QTLs, one on Chromosome (Chr) 9 (proximal-mid) and another on Chr 2 (distal), and suggestive verification was obtained for QTLs on Chrs 2 (proximal), 3, 4, 7, and 15. In addition, the possible genetic association of ethanol consumption with conditioned place preference was evaluated. Genetic correlations were estimated from BXD RI strain means, and QTL maps for these traits were compared to evaluate the possibility of a genetic association. The correlational analysis yielded a trend (r = 0.34, p = 0.09), but no statistically significant results. However, comparisons of QTL mapping results between phenotypes suggested some possible genetic overlap for these traits, both putative measures of ethanol reward. These data suggest that the determinants of these two measures are genetically diverse, but may share some common genetic elements.

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Year:  1998        PMID: 9880656     DOI: 10.1007/s003359900903

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  28 in total

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2.  Hybrid C57BL/6J x FVB/NJ mice drink more alcohol than do C57BL/6J mice.

Authors:  Yuri A Blednov; Pamela Metten; Deborah A Finn; Justin S Rhodes; Susan E Bergeson; R Adron Harris; John C Crabbe
Journal:  Alcohol Clin Exp Res       Date:  2005-11       Impact factor: 3.455

3.  Linkage analyses of stimulant dependence, craving, and heavy use in American Indians.

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Review 4.  Running is rewarding and antidepressive.

Authors:  Stefan Brené; Astrid Bjørnebekk; Elin Aberg; Aleksander A Mathé; Lars Olson; Martin Werme
Journal:  Physiol Behav       Date:  2007-05-21

5.  Identification of an acute ethanol response quantitative trait locus on mouse chromosome 2.

Authors:  K Demarest; J McCaughran; E Mahjubi; L Cipp; R Hitzemann
Journal:  J Neurosci       Date:  1999-01-15       Impact factor: 6.167

6.  Genetic relationship between ethanol-induced conditioned place preference and other ethanol phenotypes in 15 inbred mouse strains.

Authors:  Christopher L Cunningham
Journal:  Behav Neurosci       Date:  2014-05-19       Impact factor: 1.912

7.  Perturbation of chemokine networks by gene deletion alters the reinforcing actions of ethanol.

Authors:  Yuri A Blednov; Susan E Bergeson; Danielle Walker; Vania M M Ferreira; William A Kuziel; R Adron Harris
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8.  Genetic analysis of alcohol intake in recombinant inbred and congenic strains derived from A/J and C57BL/6J progenitors.

Authors:  Kathryn Gill; Alan E Boyle
Journal:  Mamm Genome       Date:  2005-05       Impact factor: 2.957

9.  Voluntary ethanol consumption by mice: genome-wide analysis of quantitative trait loci and their interactions in a C57BL/6ByJ x 129P3/J F2 intercross.

Authors:  Alexander A Bachmanov; Danielle R Reed; Xia Li; Shanru Li; Gary K Beauchamp; Michael G Tordoff
Journal:  Genome Res       Date:  2002-08       Impact factor: 9.043

10.  A verification of previously identified QTLs for cocaine-induced activation using a panel of B6.A chromosome substitution strains (CSS) and A/J x C57Bl/6J F2 mice.

Authors:  Alan E Boyle; Kathryn J Gill
Journal:  Psychopharmacology (Berl)       Date:  2009-09-23       Impact factor: 4.530

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