MOLECULAR-CLONING AND FUNCTIONAL EXPRESSION OF GLUTAMATE RECEPTOR SUBUNIT GENES

被引:836
|
作者
BOULTER, J
HOLLMANN, M
OSHEAGREENFIELD, A
HARTLEY, M
DENERIS, E
MARON, C
HEINEMANN, S
机构
[1] Molecular Neurobiology Laboratory, Salk Institute for Biological Studies, San Diego
[2] Center for Neurosciences, School of Medicine, Case Western Reserve University, Cleveland
关键词
D O I
10.1126/science.2168579
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Three closely related genes, GluR1, GluR2, and GluR3, encode receptor subunits for the excitatory neurotransmitter glutamate. The proteins encoded by the individual genes form homomeric ion channels in Xenopus oocytes that are sensitive to glutamatergic agonists such as kainate and quisqualate but not to N-methyl-D-aspartate, indicating that binding sites for kainate and quisqualate exist on single receptor polypeptides. In addition, kainate-evoked conductances are potentiated in oocytes expressing two or more of the cloned receptor subunits. Electrophysiological responses obtained with certain subunit combinations show agonist profiles and current-voltage relations that are similar to those obtained in vivo. Finally, in situ hybridization histochemistry reveals that these genes are transcribed in shared neuroanatomical loci. Thus, as with γ-aminobutyric acid, glycine, and nicotinic acetylcholine receptors, native kainate-quisqualate-sensitive glutamate receptors form a family of heteromeric proteins.
引用
收藏
页码:1033 / 1037
页数:5
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