C-elegans G protein regulator RGS-3 controls sensitivity to sensory stimuli

被引:52
作者
Ferkey, Denise M.
Hyde, Rhonda
Haspel, Gal
Dionne, Heather M.
Hess, Heather A.
Suzuki, Hiroshi
Schafer, William R.
Koelle, Michael R.
Hart, Anne C. [1 ]
机构
[1] Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Cambridge, MA 02138 USA
[3] Yale Univ, Dept Genet, New Haven, CT 06520 USA
[4] Univ Calif San Diego, Div Biol, La Jolla, CA 92093 USA
[5] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.neuron.2006.11.015
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Signal transduction through heterotrimeric G proteins is critical for sensory response across species. Regulator of G protein signaling (RGS) proteins are negative regulators of signal transduction. Herein we describe a role for C. elegans RGS-3 in the regulation of sensory behaviors. rgs-3 mutant animals fail to respond to intense sensory stimuli but respond normally to low concentrations of specific odorants. We find that loss of RGS-3 leads to aberrantly increased G protein-coupled calcium signaling but decreased synaptic output, ultimately leading to behavioral defects. Thus, rgs-3 responses are restored by decreasing G protein-coupled signal transduction, either genetically or by exogenous dopamine, by expressing a calcium-binding protein to buffer calcium levels in sensory neurons or by enhancing glutamatergic synaptic transmission from sensory neurons. Therefore, while RGS proteins generally act to downregulate signaling, loss of a specific RGS protein in sensory neurons can lead to defective responses to external stimuli.
引用
收藏
页码:39 / 52
页数:14
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