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J Physiol Volume 559, Number 2, 355-365, September 1, 2004 DOI: 10.1113/jphysiol.2004.066233
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Preferential accumulation of GABAA receptor {gamma}2L, not {gamma}2S, cytoplasmic loops at rat spinal cord inhibitory synapses

Jochen Meier and Rosemarie Grantyn

Developmental Physiology, Johannes Müller Institute, Humboldt University Medical School (Charité), D-10117 Berlin, Germany

Alternative splicing generates two variants of the GABAAR {gamma}2-subunit, {gamma}2S and {gamma}2L, which differ by insertion of the amino acid sequence LLRMFSFK into the large cytoplasmic loop between transmembrane domains 3 and 4. This additional sequence within the GABAAR {gamma}2L-subunit contains the potential protein kinase C (PKC) phosphorylation site serine 343 (Ser343). In the present study we intended to determine the capacity of these two splice variants to accumulate at inhibitory synaptic terminals and to colocalize with gephyrin, and to find out whether phosphorylation of Ser343 has any effect on GABAAR distribution. Green fluorescent protein (GFP)-tagged large cytoplasmic loops of GABAAR {gamma}2S and {gamma}2L (GFP::{gamma}2S/L) were used as surrogates for full-length receptors to study the function of the individual {gamma}2S and {gamma}2L peptides in transfected spinal cord neurones (SCNs) and COS-7 cells. It was found that GFP::{gamma}2L displayed a significantly higher capacity to accumulate at inhibitory synapses than GFP::{gamma}2S. GABAAR GFP::{gamma}2S accumulation at inhibitory postsynaptic sites was suppressed to the extent that GFP::{gamma}2S assumed a diffuse cytosolic distribution. PKC activation facilitated the postsynaptic clustering of GFP::{gamma}2L but not of GFP::{gamma}2S. This required the Ser343 residue, since substituting Ala343 for Ser343 produced a diffuse cytosolic localization pattern, like that of GFP::{gamma}2S. Furthermore, upon PKC activation Discosoma Red2-tagged GABAAR {gamma}2L (DsRed 2::{gamma}2L) colocalized with gephyrin in transfected COS-7 cells. These results support the idea that alternative splicing regulates the access of GABAARs to inhibitory postsynaptic sites in a Ser343 phosphorylation-regulated way.

(Received 8 April 2004; accepted after revision 25 June 2004; first published online 2 July 2004)
Corresponding author J. Meier: Developmental Physiology, Johannes Müller Institute, Humboldt University Medical School (Charité), Tucholskystrasse 2, D-10117 Berlin, Germany. Email: jochen.meier{at}charite.de




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