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Transcriptional response to alcohol exposure in Drosophila melanogaster

BACKGROUND: Alcoholism presents widespread social and human health problems. Alcohol sensitivity, the development of tolerance to alcohol and susceptibility to addiction vary in the population. Genetic factors that predispose to alcoholism remain largely unknown due to extensive genetic and environm...

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Autores principales: Morozova, Tatiana V, Anholt, Robert RH, Mackay, Trudy FC
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1794562/
https://www.ncbi.nlm.nih.gov/pubmed/17054780
http://dx.doi.org/10.1186/gb-2006-7-10-r95
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author Morozova, Tatiana V
Anholt, Robert RH
Mackay, Trudy FC
author_facet Morozova, Tatiana V
Anholt, Robert RH
Mackay, Trudy FC
author_sort Morozova, Tatiana V
collection PubMed
description BACKGROUND: Alcoholism presents widespread social and human health problems. Alcohol sensitivity, the development of tolerance to alcohol and susceptibility to addiction vary in the population. Genetic factors that predispose to alcoholism remain largely unknown due to extensive genetic and environmental variation in human populations. Drosophila, however, allows studies on genetically identical individuals in controlled environments. Although addiction to alcohol has not been demonstrated in Drosophila, flies show responses to alcohol exposure that resemble human intoxication, including hyperactivity, loss of postural control, sedation, and exposure-dependent development of tolerance. RESULTS: We assessed whole-genome transcriptional responses following alcohol exposure and demonstrate immediate down-regulation of genes affecting olfaction, rapid upregulation of biotransformation enzymes and, concomitant with development of tolerance, altered transcription of transcriptional regulators, proteases and metabolic enzymes, including biotransformation enzymes and enzymes associated with fatty acid biosynthesis. Functional tests of P-element disrupted alleles corresponding to genes with altered transcription implicated 75% of these in the response to alcohol, two-thirds of which have human orthologues. CONCLUSION: Expression microarray analysis is an efficient method for identifying candidate genes affecting complex behavioral and physiological traits, including alcohol abuse. Drosophila provides a valuable genetic model for comparative genomic analysis, which can inform subsequent studies in human populations. Transcriptional analyses following alcohol exposure in Drosophila implicate biotransformation pathways, transcriptional regulators, proteolysis and enzymes that act as metabolic switches in the regulation of fatty acid metabolism as important targets for future studies of the physiological consequences of human alcohol abuse.
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spelling pubmed-17945622007-02-08 Transcriptional response to alcohol exposure in Drosophila melanogaster Morozova, Tatiana V Anholt, Robert RH Mackay, Trudy FC Genome Biol Research BACKGROUND: Alcoholism presents widespread social and human health problems. Alcohol sensitivity, the development of tolerance to alcohol and susceptibility to addiction vary in the population. Genetic factors that predispose to alcoholism remain largely unknown due to extensive genetic and environmental variation in human populations. Drosophila, however, allows studies on genetically identical individuals in controlled environments. Although addiction to alcohol has not been demonstrated in Drosophila, flies show responses to alcohol exposure that resemble human intoxication, including hyperactivity, loss of postural control, sedation, and exposure-dependent development of tolerance. RESULTS: We assessed whole-genome transcriptional responses following alcohol exposure and demonstrate immediate down-regulation of genes affecting olfaction, rapid upregulation of biotransformation enzymes and, concomitant with development of tolerance, altered transcription of transcriptional regulators, proteases and metabolic enzymes, including biotransformation enzymes and enzymes associated with fatty acid biosynthesis. Functional tests of P-element disrupted alleles corresponding to genes with altered transcription implicated 75% of these in the response to alcohol, two-thirds of which have human orthologues. CONCLUSION: Expression microarray analysis is an efficient method for identifying candidate genes affecting complex behavioral and physiological traits, including alcohol abuse. Drosophila provides a valuable genetic model for comparative genomic analysis, which can inform subsequent studies in human populations. Transcriptional analyses following alcohol exposure in Drosophila implicate biotransformation pathways, transcriptional regulators, proteolysis and enzymes that act as metabolic switches in the regulation of fatty acid metabolism as important targets for future studies of the physiological consequences of human alcohol abuse. BioMed Central 2006 2006-10-20 /pmc/articles/PMC1794562/ /pubmed/17054780 http://dx.doi.org/10.1186/gb-2006-7-10-r95 Text en Copyright © 2006 Morozova et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Morozova, Tatiana V
Anholt, Robert RH
Mackay, Trudy FC
Transcriptional response to alcohol exposure in Drosophila melanogaster
title Transcriptional response to alcohol exposure in Drosophila melanogaster
title_full Transcriptional response to alcohol exposure in Drosophila melanogaster
title_fullStr Transcriptional response to alcohol exposure in Drosophila melanogaster
title_full_unstemmed Transcriptional response to alcohol exposure in Drosophila melanogaster
title_short Transcriptional response to alcohol exposure in Drosophila melanogaster
title_sort transcriptional response to alcohol exposure in drosophila melanogaster
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1794562/
https://www.ncbi.nlm.nih.gov/pubmed/17054780
http://dx.doi.org/10.1186/gb-2006-7-10-r95
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