Functional roles for redox genes in ethanol sensitivity in Drosophila

被引:11
作者
Awofala, Awoyemi A. [2 ,3 ]
Davies, Jane A. [2 ]
Jones, Susan [1 ,2 ]
机构
[1] James Hutton Inst, Dundee DD2 5DA, Scotland
[2] Univ Sussex, Sch Life Sci, Brighton BN1 9QG, E Sussex, England
[3] Tai Solarin Univ Educ, Dept Biol Sci, Ijebu, Ogun State, Nigeria
关键词
Ethanol; Drosophila; Ageing; Microarray; Oxidative stress; Glutathione metabolism; DIFFERENTIAL EXPRESSION DISCOVERIES; SIGNALING PATHWAY; OXIDATIVE STRESS; ALCOHOL EXPOSURE; KINASE; REPRODUCIBILITY; BIOINFORMATICS; MICROARRAY; RECEPTORS; TOLERANCE;
D O I
10.1007/s10142-012-0272-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Whilst the effects and associated costs of excessive alcohol consumption in the human population are obvious at one level, the roles played by genetic factors at the molecular level are still unclear. Drosophila melanogaster has an alcohol response comparable to humans and is used as a genetic model to study the functional roles of genes regulated in response to ethanol. In the current study, the biological processes associated with behavioural responses to acute alcohol exposure in Drosophila have been analysed using whole genome expression profiling. Ethanol response genes differentially expressed (a) at a single time point (2 h) and (b) in a time series (0-4 h) were identified using microarrays. In addition, a subset of differentially expressed genes was validated using behavioural sedation and recovery assays. The study shows that genes involved in redox processes, neuron development, and specific signalling and metabolic pathways (including glutathione metabolism) form part of the response to ethanol in Drosophila. Biological processes for the regulation of oxidative stress are the common functional denominator of many of the ethanol response genes identified. These upregulated genes work to rescue cells from oxidative stress and its consequences such as protein misfolding, apoptosis and ageing. In the current study, an enrichment of Drosophila genes linked to ageing is observed for the first time. The functional genomics data revealed by such studies can be used to predict transcription networks of ethanol response genes, but the future lies in mapping these networks to the human population, with the ultimate aim of identifying genetic factors for alcohol use disorders.
引用
收藏
页码:305 / 315
页数:11
相关论文
共 47 条
  • [1] Differential Changes in MAP Kinases, Histone Modifications, and Liver Injury in Rats Acutely Treated With Ethanol
    Aroor, Annayya R.
    James, Taryn T.
    Jackson, Daniel E.
    Shukla, Shivendra D.
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2010, 34 (09) : 1543 - 1551
  • [2] MAP kinase signaling in diverse effects of ethanol
    Aroor, AR
    Shukla, SD
    [J]. LIFE SCIENCES, 2004, 74 (19) : 2339 - 2364
  • [3] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [4] The Heat Shock Protein 26 Gene Is Required for Ethanol Tolerance in Drosophila
    Awofala, Awoyemi A.
    Jones, Susan
    Davies, Jane A.
    [J]. JOURNAL OF EXPERIMENTAL NEUROSCIENCE, 2011, 5 : 31 - 44
  • [5] Expression of Drosophila Cabut during early embryogenesis, dorsal closure and nervous system development
    Belacortu, Yaiza
    Weiss, Ron
    Kadener, Sebastian
    Paricio, Nuria
    [J]. GENE EXPRESSION PATTERNS, 2011, 11 (3-4) : 190 - 201
  • [6] CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING
    BENJAMINI, Y
    HOCHBERG, Y
    [J]. JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) : 289 - 300
  • [7] The Gene Ontology in 2010: extensions and refinements The Gene Ontology Consortium
    Berardini, Tanya Z.
    Li, Donghui
    Huala, Eva
    Bridges, Susan
    Burgess, Shane
    McCarthy, Fiona
    Carbon, Seth
    Lewis, Suzanna E.
    Mungall, Christopher J.
    Abdulla, Amina
    Wood, Valerie
    Feltrin, Erika
    Valle, Giorgio
    Chisholm, Rex L.
    Fey, Petra
    Gaudet, Pascale
    Kibbe, Warren
    Basu, Siddhartha
    Bushmanova, Yulia
    Eilbeck, Karen
    Siegele, Deborah A.
    McIntosh, Brenley
    Renfro, Daniel
    Zweifel, Adrienne
    Hu, James C.
    Ashburner, Michael
    Tweedie, Susan
    Alam-Faruque, Yasmin
    Apweiler, Rolf
    Auchinchloss, Andrea
    Bairoch, Amos
    Barrell, Daniel
    Binns, David
    Blatter, Marie-Claude
    Bougueleret, Lydie
    Boutet, Emmanuel
    Breuza, Lionel
    Bridge, Alan
    Browne, Paul
    Chan, Wei Mun
    Coudert, Elizabeth
    Daugherty, Louise
    Dimmer, Emily
    Eberhardt, Ruth
    Estreicher, Anne
    Famiglietti, Livia
    Ferro-Rojas, Serenella
    Feuermann, Marc
    Foulger, Rebecca
    Gruaz-Gumowski, Nadine
    [J]. NUCLEIC ACIDS RESEARCH, 2010, 38 : D331 - D335
  • [8] STRIPE-SPECIFIC REGULATION OF PAIR-RULE GENES BY HOPSCOTCH, A PUTATIVE JAK FAMILY TYROSINE KINASE IN DROSOPHILA
    BINARI, R
    PERRIMON, N
    [J]. GENES & DEVELOPMENT, 1994, 8 (03) : 300 - 312
  • [9] Glutathione-S-transferase expression in the brain:: possible role in ethanol preference and longevity
    Bjork, K.
    Saarikoski, S. T.
    Arlinde, C.
    Kovanen, L.
    Osei-Hyiaman, D.
    Ubaldi, M.
    Reimers, M.
    Hyytia, P.
    Heilig, M.
    Sommer, W. H.
    [J]. FASEB JOURNAL, 2006, 20 (11) : 1826 - 1835
  • [10] The role of oxidative damage and stress in aging
    Bokov, A
    Chaudhuri, A
    Richardson, A
    [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 2004, 125 (10-11) : 811 - 826