Alternate splicing and expression of the glutamate transporter EAAT5 in the rat retina

被引:11
|
作者
Lee, Aven [1 ]
Anderson, Ashley R. [1 ]
Barnett, Nigel L. [1 ,2 ]
Stevens, Melissa G. [1 ]
Pow, David V. [1 ,3 ,4 ]
机构
[1] Univ Queensland, UQ Ctr Clin Res, Brisbane, Qld 4029, Australia
[2] Queensland Eye Inst, Brisbane, Qld, Australia
[3] RMIT Sch Med Sci, Bundoora, Vic 3083, Australia
[4] Heath Innovat Res Inst, Bundoora, Vic 3083, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Slc1a7; Excitotoxicity; Cloning; Glutamate; Receptor; Alternative splicing; AMYOTROPHIC-LATERAL-SCLEROSIS; NERVOUS-SYSTEM; SKIPPING FORM; GLT-1; VARIANTS; BRAIN; CLONING; RNA; IMMUNOLOCALIZATION; LOCALIZATION;
D O I
10.1016/j.gene.2012.07.010
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Excitatory amino acid transporter 5 (EAAT5) is an unusual glutamate transporter that is expressed in the retina, where it is localised to two populations of glutamatergic neurons, namely the bipolar neurons and photoreceptors. EAAT5 exhibits two distinct properties, acting both as a slow glutamate transporter and as a glutamate-gated inhibitory receptor. The latter property is attributable to a co-associated chloride conductance. EAAT5 has previously been thought to exist only as a full-length form. We now demonstrate by PCR cloning and sequencing, the presence of five novel splice variant forms of EAAT5 which skip either partial or complete exons in the rat retina. Furthermore, we demonstrate that each of these variants is expressed at the protein level as assessed by Western blotting using splice-specific antibodies that we have generated. We conclude that EAAT5 exists in multiple spliced forms, and propose, based upon retention or absence of key structural features, that these variant forms may potentially exhibit distinct properties relative to the originally described form of EAAT5. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:283 / 288
页数:6
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