Literature DB >> 26170296

Rsu1 regulates ethanol consumption in Drosophila and humans.

Shamsideen A Ojelade1, Tianye Jia2, Aylin R Rodan3, Tao Chenyang4, Julie L Kadrmas5, Anna Cattrell2, Barbara Ruggeri2, Pimphen Charoen6, Hervé Lemaitre7, Tobias Banaschewski8, Christian Büchel9, Arun L W Bokde10, Fabiana Carvalho2, Patricia J Conrod11, Herta Flor8, Vincent Frouin12, Jürgen Gallinat13, Hugh Garavan14, Penny A Gowland15, Andreas Heinz13, Bernd Ittermann15, Mark Lathrop16, Steven Lubbe2, Jean-Luc Martinot7, Tomás Paus17, Michael N Smolka18, Rainer Spanagel8, Paul F O'Reilly2, Jaana Laitinen19, Juha M Veijola20, Jianfeng Feng21, Sylvane Desrivières2, Marjo-Riitta Jarvelin22, Gunter Schumann23, Adrian Rothenfluh24.   

Abstract

Alcohol abuse is highly prevalent, but little is understood about the molecular causes. Here, we report that Ras suppressor 1 (Rsu1) affects ethanol consumption in flies and humans. Drosophila lacking Rsu1 show reduced sensitivity to ethanol-induced sedation. We show that Rsu1 is required in the adult nervous system for normal sensitivity and that it acts downstream of the integrin cell adhesion molecule and upstream of the Ras-related C3 botulinum toxin substrate 1 (Rac1) GTPase to regulate the actin cytoskeleton. In an ethanol preference assay, global loss of Rsu1 causes high naïve preference. In contrast, flies lacking Rsu1 only in the mushroom bodies of the brain show normal naïve preference but then fail to acquire ethanol preference like normal flies. Rsu1 is, thus, required in distinct neurons to modulate naïve and acquired ethanol preference. In humans, we find that polymorphisms in RSU1 are associated with brain activation in the ventral striatum during reward anticipation in adolescents and alcohol consumption in both adolescents and adults. Together, these data suggest a conserved role for integrin/Rsu1/Rac1/actin signaling in modulating reward-related phenotypes, including ethanol consumption, across phyla.

Entities:  

Keywords:  actin; addiction; alcohol; genetics

Mesh:

Substances:

Year:  2015        PMID: 26170296      PMCID: PMC4522778          DOI: 10.1073/pnas.1417222112

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


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