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The Journal of Neuroscience, June 16, 2004, 24(24):5570-5578; doi:10.1523/JNEUROSCI.1301-04.2004
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Neurobiology of Disease
The Juvenile Myoclonic Epilepsy GABAA Receptor  1 Subunit Mutation A322D Produces Asymmetrical, Subunit Position-Dependent Reduction of Heterozygous Receptor Currents and 1 Subunit Protein Expression
Martin J. Gallagher,1
Luyan Song,1
Fazal Arain,1 and
Robert L. Macdonald1,2,3
Departments of 1Neurology, 2Molecular Physiology and Biophysics, and 3Pharmacology, Vanderbilt University, Nashville, Tennessee 37212
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Abstract
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Individuals with autosomal dominant juvenile myoclonic epilepsy are heterozygous for a GABAA receptor  1 subunit mutation (1A322D). GABAA receptor   subunits are arranged around the pore in a ---- sequence (counterclockwise from the synaptic cleft). Therefore, each 1 subunit has different adjacent subunits, and heterozygous expression of 1(A322D), , and subunits could produce receptors with four different subunit arrangements: -1--1- (wild type); -1(A322D)--1- (Het); -1--1(A322D)- (Het);-1(A322D)--1(A322D)- (homozygous). Expression of a 1:1 mixture of wild-type and1(A322D) subunits with 2S and 2S subunits (heterozygous transfection) produced smaller currents than wild type and much larger currents than homozygous mutant transfections. Western blot and biotinylation assays demonstrated that the amount of total and surface 1 subunit from heterozygous transfections was also intermediate between those of wild-type and homozygous mutant transfections. 1(A322D) mutations were then made in covalently tethered triplet (2S-2S-1) and tandem (2S-1) concatamers to target selectively 1(A322D) to each of the asymmetric 1 subunits. Coexpression of mutant and wild-type concatamers resulted in expression of either Het or Het receptors. Het currents were smaller than wild type and much larger than Het and homozygous currents. Furthermore, Het transfections contained less - concatamer than wild type but more than both Het and homozygous mutant transfections. Thus, whole-cell currents and protein expression of heterozygous 1(A322D)2S2S receptors depended on the position of the mutant 1 subunit, and GABAA receptor currents in heterozygous individuals likely result primarily from wild-type and Het receptors with little contribution from Het and homozygous receptors.
Key words: juvenile myoclonic epilepsy; chloride ion channel; GABAA receptors; mutant; myoclonus; patch clamp; protein; concatamer
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Introduction
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Juvenile myoclonic epilepsy (JME) is a generalized epilepsy syndrome that accounts for 5-10% epilepsy patients and is characterized by myoclonic, tonic-clonic, and absence seizures as well as typical electroencephalographic findings (Genton and Gelisse, 2001 ). Recently, a missense mutation (A322D) in the GABAA receptor 1 subunit gene (GABRA1) was found in all family members who were affected with an autosomal dominant form of JME (ADJME) (Cossette et al., 2002).
GABAA receptors, the major inhibitory neurotransmitter receptors in the mammalian CNS, are pentameric ligand-gated chloride ion channels. The five subunits arise from seven subunit families that contain multiple subtypes (1-6, 1-3, 1-3,  1,  1,  1,  1). GABAA receptors assemble in a limited number of subunit combinations, with the most prevalent combination consisting of two 1 subunits, two 2 subunits, and one 2 subunit (McKernan and Whiting, 1996). The arrangement of each subunit around the pore (2-1-2-1-2; counterclockwise when viewed extracellularly) has been determined (Tretter et al., 1997; Baumann et al., 2001, 2002). We designated the subunit between the subunits, the subunit, and the subunit between the and subunits, the subunit.
All patients with ADJME were heterozygous for the 1(A322D) mutation and, therefore, had one wild-type and one mutant 1 subunit allele. These patients could express four different 1 GABAA receptor phenotypes: wild-type 1, heterozygous 1(A322D) (Het), heterozygous 1(A322D) (Het), and homozygous 1(A322D). Previous studies demonstrated that homozygous 1(A322D) receptors had  10% of the peak current and an 200-fold higher GABA EC50 value compared with wild-type 1 receptors; however, no unique heterozygous response was identified (Cossette et al., 2002). Because patients with ADJME were heterozygous, not homozygous, for the 1(A322D) mutation, it raises the questions what is the abnormal heterozygous 1(A322D) receptor phenotype and do the mutations have a positional effect on receptor assembly, transport to the cell surface, and receptor function? To characterize the properties of heterozygous 1(A322D) GABAA receptors, we transfected HEK293T cells with wild-type 2S and 2S subunits and wild-type 1 subunit, 1(A322D) subunit, or a 1:1 mixture (heterozygous expression) of wild-type 1 and 1(A322D) subunits and measured their peak currents and current kinetics after rapid, saturating GABA application. We then measured their levels of 1 subunit protein by using Western blot and biotinylation assays.
Next, we characterized the same properties of Het and Het receptors by individually mutating the 1 subunit in tethered triplet [2S-2-1(A322D)] and tandem [2-1(A322D)] constructs. Because functional ion channels only form from association of one triplet (2S-2-1) and one tandem (2-1) construct (Baumann et al., 2002), expression of mutated triplet [2S-2-1(A322D)] with wild-type tandem (2-1) constructs forced assembly of Het receptors, whereas expression of wild-type triplet (2S-2-1) with mutated tandem [2-1(A322D)] constructs forced assembly of Het receptors.
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Materials and Methods
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Expression of recombinant GABAA receptors. The cDNAs encoding human 1, 2S, and 2S subunits in pcDNA3.1 plasmid were a gift from Dr. Matthew Jones (University of Wisconsin, Madison, WI). The construction of the cDNAs encoding tethered rat subunits (2S-2-1) and (2-1) in pCMV vector has been described (Baumann et al., 2002) and were kindly provided to us by Dr. Erwin Sigel (University of Bern, Bern, Switzerland). Here, the 2S-2-1 and 2-1 constructs will be abbreviated as -- and -, respectively. 1(A322D) point mutations were made using the QuikChange site-directed mutagenesis kit (Stratagene, La Jolla, CA) and were confirmed by DNA sequencing. The details of cell culture and GABAA receptor expression have been described previously (Angelotti et al., 1993). Human embryonic kidney cells (HEK293T; a gift from P. Connely, COR Therapeutics, San Francisco, CA) were grown in DMEM (Invitrogen, Bethesda, MD) with 10% FBS (Invitrogen) and 100 IU/ml each of penicillin and streptomycin (Invitrogen) at 37°C in 5% CO2/95% air. Cells were transfected in 6 cm culture dishes (Corning Glass Works, Corning, NY) using a modified calcium phosphate method. For the untethered experiments, cells were cotransfected with 4 µg:4 µg:4 µg:2 µg (1:2S:2S:pHook) (Invitrogen, Carlsbad, CA), which is used for immunomagnetic separation (Greenfield et al., 1997). For the tethered experiments, to express -- and : in 1:1 molar ratios, cells were transfected with 4.8 µg:4 µg:2 µg (--:-:pHook). Four hours after DNA addition, the cells were shocked with 15% glycerol in N, N-bis(2-hydroxyethyl)-2-aminoethanesulfonic acid-buffered saline for 30 sec. Approximately 20 hr after transfection, cells were trypsinized, centrifuged (400 x g), and incubated with hapten-coated magnetic beads at 37°C for 30 min to allow the pHook antibody of the positively transfected cells to bind to the beads. The bound cells were then isolated using a magnetic stand and plated on 35 mm culture dishes.
Electrophysiology experiments. Electrophysiological experiments were performed 20-36 hr after plating on 35 mm dishes. The external recording solution consisted of the following (in mM): 142 NaCl, 8 KCl, 6 MgCl2, 1 CaCl2, 10 glucose, and 10 HEPES, pH 7.4 (osmolarity, 323-330 mOsm). The intrapipette solution contained (in mM): 153 KCl, 1 MgCl2, 5 EGTA, 10 HEPES, and 2 MgATP, pH 7.3 (osmolarity, 300-316 mOsm). This combination of external and intrapipette solutions produced a chloride equilibrium potential (ECl) of approximately zero. Recording pipettes were pulled from borosilicate capillary glass (Fisher, Pittsburgh, PA) on a Sutter P-2000 micropipette electrode puller (Sutter Instrument, San Rafael, CA). GABAA receptor currents were recorded using a lifted whole-cell patch-clamp technique with cells clamped at -20 mV during the recordings. Recordings were obtained from lifted whole cells rather than macropatches, because it allowed measurement of larger currents and avoided the cytoskeletal disruption of detached membrane patches. Lifting the cell from the surface of the dish improved solution exchange time and allowed better resolution of fast (<20 msec) components of desensitization compared with whole-cell recordings when the cell is attached to the dish (Bianchi and Macdonald, 2002; Hinkle et al., 2003). Signals were processed using a List EPC-7 amplifier (List Electronics, Darmstadt, Germany) in voltage-clamp mode, sampled at 10 kHz, and recorded on a computer. GABA was applied to the cells (via gravity) using a rapid perfusion system consisting of pulled multibarrel square glass (final size, 200-300 µm) connected to a Perfusion Fast-Step (Warner Instrument, Hamden, CT) (Hinkle et al., 2003). The solution exchange time was determined by stepping a 10% dilute external solution across the open electrode tip to measure a liquid junction current. The 10-90% rise times for solution exchange were consistently  1.0 msec; it is assumed that the exchange time for a whole cell is significantly greater. Because the cells adjust their position within the solution flow after being detached from the dish surface, 1 mM GABA was applied for 400 msec every 30 sec until reproducible current traces were obtained; the first of the reproducible traces was used for analysis of current kinetics.
Current amplitudes and rapid kinetic properties were measured on a computer using Clampfit 9.0 (Axon Instruments, Foster City, CA). Only cells with  0.5 G seals were included in the analyses. For the untethered experiments, 15% of the cells lacked a fast component of desensitization; these were not included in the analyses. All the tethered GABAA receptors had a fast component of desensitization. Activation was measured as the 10-90% rise time from baseline to peak current. The desensitization and deactivation time courses were fit using the Levenberg-Marquardt least squares method to the equation  anexp(-t/ n), where n is the number of exponential components, a is the amplitude of that component, t is time (milliseconds), and is the desensitization time constant. Time constants were constrained to be positive.
It has been shown that subunit-containing GABAA receptors have at least four components of desensitization (Bianchi and Macdonald, 2002) and that their desensitization time course after 400 msec applications of 1 mM GABA can typically be best fit by two exponential functions, whereas the desensitization time course after 6 sec GABA applications can be best fit by three exponential functions. Therefore, we fit the desensitization and deactivation time courses of 400 msec GABA applications to two exponential components and the desensitization time course of 6000 msec GABA applications to three exponential components. The weighted deactivation time, weight, was calculated [a1/(a1 + a2) x 1 + a2/(a1 + a2) x 2].
Concentration-response curves were obtained from the peak GABAA receptor currents evoked by increasing GABA concentrations. The EC50 value was calculated by fitting the peak currents to the equation: I = Imax/[1 + (EC50/(GABA))Hill Slope], where I is the peak current at a given GABA concentration and Imax is the peak current at the maximal GABA concentration.
Immunoblots. Western blots were performed essentially as described previously (Baumann et al., 2001; Hahn et al., 2003). Transfected cells were solubilized for 30 min in 20 mM Tris, 20 mM EGTA, 1 mM DTT, 1 mM benzamidine, 100 µM PMSF, 5 µg/ml leupeptin, 5 µg/ml pepstatin, 1% Triton X-100, and either with or without 0.5% SDS. Protein concentrations were measured using the Micro BCA Protein assay (Pierce, Rockford, IL). The lysate was centrifuged at 14,000 x g for 30 min, and the supernatant was fractionated by 7.5% SDS-PAGE and electrotransferred to polyvinylidene fluoride membranes (Millipore, Billerica, MA). The membranes were incubated with a monoclonal antibody against either the GABAA receptor 1 subunit (20 µg/ml, clone BD24; Chemicon, Temecula, CA) or 2/3 subunit (1 µg/ml, clone 62-3G1; Upstate, Charlottesville, VA) and then were incubated with a HRP-coupled anti-mouse secondary antibody (1:6000 dilution; Jackson ImmunoResearch, West Grove, PA). GABAA receptor 1 subunits and - concatamers were then visualized with a chemiluminescent detection system (Bio-Rad, Hercules, CA) using x-ray film (Pierce). The x-ray film was scanned into a computer, and the immunopositive bands were quantified using the software Quantity One 4.5.0 (Bio-Rad). The rectangular volume (pixel intensity times square millimeter) of each band was normalized to the volume of the wild-type band.
Cell surface biotinylation. Live, transfected cells were washed with PBS (pH 7.4; Invitrogen) containing 0.1 mM CaCl2 and1mM MgCl2 and then incubated with sulfosuccinimidyl-2-(biotinamido)ethyl-1,3-dithiopropionate (sulfo-NHS-SS-biotin, 1.5 mg/ml; Pierce) for 1 hr at 4°C. The sulfo-NHS-SS-biotin was quenched with PBS containing 0.1 mM glycine. The cells were washed and then lysed as described above and incubated with immobilized strepavidin (Pierce) for 1 hr at room temperature. The biotinylated proteins were eluted from the strepavidin by incubation with Laemmli sample buffer at 70°C and fractionated on Western blots as described above.
Data analysis. Values are reported as means ± SEM. Statistical significance was evaluated using the Student's unpaired t test (GraphPad Prism; Graph Pad, San Diego, CA), with Welch's correction used if the variances were unequal (Bartlett's test; GraphPad Prism). Determinations of whether data deviated from Gaussian distributions were made using the Kolmogorov-Smirnov test (GraphPad Prism).
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Results
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Transient kinetic properties of heterozygous 1(A322D)S22 currents were similar to wild-type 1S22S but differed from those of homozygous 1(A322D)S22S currents
Whole-cell currents were recorded from lifted HEK293T cells transfected with wild-type 2S and 2S subunits and wild-type 1 subunit (Fig. 1A, wild-type transfection), a 1:1 mixture of wild-type and mutant 1 subunits (Fig. 1B, heterozygous transfection), or mutant 1(A322D) subunit (Fig. 1C, homozygous transfection). The heterozygous transfection would be predicted to contain a binomial mixture of receptors with wild-type, homozygous mutant Het and Het receptors, and thus peak currents and current kinetics would be predicted to be the sum of currents obtained separately from each of these receptors. Cells were exposed to 1 mM GABA, approximating the peak GABA concentration at a synapse, for 400 msec. Previous studies have shown that neurons with endogenous GABAA receptors (Mellor and Randall, 1997; Zhu and Vicini, 1997) as well as cells expressing recombinant GABAA receptors (Gingrich and Burkat, 1998; Haas and Macdonald, 1999; Bianchi and Macdonald, 2002; Scheller and Forman, 2002) with , , and subunits have fast (<20 msec), intermediate (200 msec), slow ( 1000 msec), and ultraslow (10,000 msec) components of desensitization when GABA is applied for several seconds. With the briefer (400 msec) GABA applications used in this study, only the fast and intermediate phases of desensitization could be resolved.
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Figure 1. Whole-cell currents of untethered GABAA receptors. Representative current traces obtained from wild-type (A), heterozygous (B), or homozygous (C) mutant transfections after a 400 msec step into 1 mM GABA. The black trace in C is depicted on the same voltage scale (top scale bar) as the traces in A and B, but the gray trace is plotted in an expanded scale (bottom scale bar) to display the time course of the current kinetics. D, The mean peak currents are depicted ±SEM. Peak currents from heterozygous transfections (n = 16) were significantly larger than homozygous mutant peak currents (n = 5; p < 0.001) and significantly smaller than wild-type peak currents (n = 17; p < 0.05). E, The GABA EC50 values for wild-type ( ), heterozygous ( ), and homozygous ( ) mutant transfections were determined by 6 sec, rapid-perfusion, whole-cell response in increasing GABA concentrations. Cells were voltage clamped at -20 mV. Currents were normalized to the maximal peak current for each cell, and the EC50 values were calculated and fit as described in Materials and Methods.
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The transient kinetic properties of wild-type (Fig. 1A) and heterozygous 1(A322D)S22S (Fig. 1B) currents were similar to each other but differed substantially from those of homozygous 1(A322D)S22S currents (Fig. 1C; Table 1). The 10-90% activation times of heterozygous (4.5 ± 0.5 msec) receptor currents were significantly faster than those of homozygous (53.9 ± 4.7 msec) 1(A322D)S22S currents (p < 0.001) but were not significantly different from wild-type (4.0 ± 0.8 msec) currents. Heterozygous receptor currents differed from homozygous 1(A322D)S22S currents, but not wild-type currents, by having both fast and intermediate phases of desensitization. Heterozygous currents had faster deactivation times (147 ± 10 msec) than wild-type currents (267 ± 50 msec) but had slower deactivation times than homozygous currents (31 ± 5 msec). The slower activation, lack of fast and intermediate desensitization, and faster deactivation of homozygous receptor currents were also present when tested with 10 mM GABA (data not shown).
Six-second applications of 1 or 10 mM GABA demonstrated that heterozygous currents had a slow component of desensitization with a time constant (2462 ± 45 msec) that was similar to those of wild-type (3856 ± 1092 msec; p > 0.05) and homozygous mutant (3463 ± 632 msec; p > 0.05) currents (supplementary Table 1; available at www.jneurosci.org). Because homozygous mutant currents lacked fast and intermediate components of desensitization, their component of slow desensitization (70 ± 3%) was greater than wild-type (38 ± 2%) or heterozygous (35 ± 6%) currents (p < 0.001), but their component of total desensitization (70 ± 3%) was less than heterozygous (87 ± 2%) or wild-type (82 ± 3%) currents (p < 0.01).
Peak amplitudes of heterozygous 1(A322D)S22S currents were intermediate between wild-type and homozygous 1(A322D)S22S currents
It was previously reported that maximal whole-cell peak currents from HEK293 cells transfected with homozygous 1(A322D)2S2L receptors were 10% of those of wild-type 12S2L receptors and that heterozygous 1(A322D) receptor peak currents resembled either wild-type or homozygous 1(A322D)S22S currents without an intermediate response (Cossette et al., 2002). We determined the mean maximal whole-cell peak currents from cells after heterozygous transfections and compared them with currents obtained from cells after wild-type and homozygous 1(A322D)S22S mutant transfections (Fig. 1D). We found that heterozygous 1(A322D) peak currents (1404 ± 271 pA) were significantly smaller than wild-type peak currents (2820 ± 551 pA; p < 0.05) but substantially larger than homozygous 1(A322D) peak currents (161 ± 62 pA; p < 0.001). The peak homozygous 1(A322D) currents were 6% that of wild-type currents, similar to a previous report (Cossette et al., 2002).
The GABA EC50 values of homozygous and heterozygous 1(A322D) currents were higher than wild-type 12S2S currents
We determined the GABA EC50 values for the whole-cell currents from cells obtained from wild-type, heterozygous, and homozygous transfections (Fig. 1E). Although the GABA EC50 values for cells from heterozygous transfections (22 ± 3 µM) was almost twice that of wild-type receptors (13 ± 3 µM), the difference did not reach significance (p = 0.06; n = 5). As reported previously (Cossette et al., 2002), homozygous mutant receptors had a significantly higher GABA EC50 values (197 ± 66 µM) than wild-type receptors (13 ± 3 µM; p < 0.001). Cells from the wild-type and heterozygous transfection conditions had maximal currents at GABA concentrations 1 mM, the presumed synaptic GABA concentration and the concentration of GABA that was used in this study to measure both peak currents and rapid current kinetics. The mean Hill coefficient of the homozygous mutant receptor currents (0.8 ± 0.1) was smaller than wild-type receptor currents (p < 0.05), and the mean Hill coefficient of the cells from the heterozygous transfections (1.1 ± 0.2) was between wild-type and homozygous mutant receptor currents, but these differences were not statistically significant (p > 0.05).
1(A322D) reduced the amount of total and surface 1 subunit
To determine the effect of the 1(A322D) mutation on the expression of the 1 subunit, HEK293T cells were transfected with wild-type 2 and 2 subunits and either wild-type 1 subunit (WT), a 1:1 mixture of wild-type and 1(A322D) subunits (Het), 1(A322D) subunit (Hom), or only the 2 and 2 subunits but with no 1 () subunits, and Western blot analyses were performed using a monoclonal antibody targeted against the N terminus of the 1 subunit (Fig. 2A). In these blots of whole-cell lysates (20 µg of protein), the only specific immunoreactive band was present at 50 kDa, the size of the 1 subunit. The bands were quantified, and the band volumes (intensity times square millimeter) were normalized to the wild-type band for each experiment. The heterozygous 1(A322D) transfection had reduced 1 subunit relative to wild-type receptor transfection (56 ± 13% wild-type expression; n = 4) but contained more 1 subunit than the homozygous mutant transfection (6 ± 4% wild-type expression; n = 5).
To determine the effect of the 1(A322D) mutation on surface expression of receptors, transfected HEK293T cells were incubated with sulfo-NHS-SS-biotin, and the biotinylated protein was analyzed by Western blots (Fig. 2B). Heterozygous 1(A322D) transfections had reduced surface 1 subunit relative to wild-type transfections (22 ± 10% wild type; n = 3) and more surface 1 subunit than homozygous mutant transfections (3 ± 2% wild-type expression; n = 3).
These results differ from those previously reported, which showed similar 1 subunit protein expression in wild-type and homozygous mutant receptors (Cossette et al., 2002). Although it was unlikely that a single missense mutation in the M3 domain reduced antibody recognition at the N terminus on Western blots, we repeated the experiments using the same polyclonal antibody used in the previous studies and found that none of the immunoreactive bands were specific (data not shown). The previous studies (Cossette et al., 2002) also used high concentrations of denaturing detergents that could increase detection of mutant 1 subunits if they were sequestered in subcellular compartments that were not solubilized with nondenaturing detergents. Therefore, we repeated the Western blots using 0.5% SDS and found results identical to those depicted in Figure 2A.
Tethered heterozygous 1(A322D)2S2S receptor expression
The electrophysiological properties of both wild-type and homozygous mutant receptors could be definitively characterized in the previous sections because transfection with only wild-type 1, 2, and 2 subunits produced only wild-type receptors and transfection of only 1(A322D), 2, and 2 subunits produced only homozygous mutant receptors. In contrast, the properties of Het and Het receptors could not be determined definitively because heterozygous transfection with a 1:1 mixture of wild-type 1 and mutant 1(A322D) subunits (heterozygous expression) could produce receptors with all four possible wild-type and mutant 1 subunit combinations (w/w, wt/, wt/, Het/). To determine the properties of Het and Het receptors, we forced their assembly using -- and - constructs. Transfection of mutant --(A322D) triplet concatamers with wild-type - tandem concatamers produced Het receptors, and transfection of the wild-type -- triplet concatamer with the mutant -(A322D) tandem concatamer produced Het receptors.
To confirm that only pentameric Het and Het receptors were formed and that there were no substantial currents arising from - tetramers, -- hexamers or pentamers formed from concatamer breakdown, HEK293T cells were transfected with twice the usual amount of (8.0 µg) wild-type - construct without the -- construct, and no current was detected (n = 3). Similarly, when cells were transfected with twice the usual amount (9.6 µg) of wild-type -- cDNA without the - construct, three cells had no current and two cells had very small peak currents of 32 and 33 pA. In contrast, all cells transfected with a 1:1 molar ratio of -- and - cDNAs produced much larger currents (mean, 967 ± 279 pA). This demonstrated that in HEK293T cells as in Xenopus oocytes (Baumann et al., 2001, 2002), expression of exactly one triplet and one tandem construct is required to produce functional GABAA receptors.
The transient kinetic properties of tethered Het currents differ from those of Het and wild-type currents
Representative current traces for tethered wild-type, Het, and Het currents after 400 msec applications of 1 mM GABA for are presented in Figure 3. Currents were obtained from all cells expressing wild-type (Fig. 3A) or Het (Fig. 3B) receptors but from only three of the eight cells expressing Het receptors (Fig. 3C). Both the wild-type and Het currents had fast and intermediate components of desensitization. The low current amplitudes of the Het receptors prohibited analyses of their current kinetics, and thus it is not known whether these currents differed from currents recorded from cells transfected with only wild-type -- subunits.
Peak amplitudes of tethered Het, Het, and wild-type currents differed
We determined the mean peak currents of tethered wild-type, Het, and Het receptors after 400 msec applications of 1 mM GABA (Fig. 3D). The mean peak current of Het receptors (335 ± 87 pA) was smaller than that of wild-type receptors (967 ± 279 pA; p < 0.05). Het receptors had significantly smaller peak currents (9 ± 5 pA) than either wild-type (967 ± 279 pA) or Het (335 ± 87 pA) receptors (p < 0.01). The variability of the peak currents from the wild-type tethered receptors (coefficient of variation, 115%) was larger than that of wild-type untethered receptors (coefficient of variation, 80%), a finding similar to that obtained in Xenopus oocytes (Baumann et al., 2002), which may reflect inefficient assemblies and thus more cell-to-cell variability of expression of the tethered constructs. Homozygous tethered receptors were expressed by cotransfecting the mutant triplet --(A322D) construct with the mutant tandem -(A322D) construct, but no currents were obtained, a result that was not surprising considering the very small Het peak currents.
Het currents had larger components of fast desensitization than wild-type currents
Activation, desensitization, and deactivation current kinetics were measured in lifted cells by applying 1 mM GABA for 400 msec to the tethered GABAA receptors. All of the tethered wild-type and Het currents had both a fast and an intermediate component of desensitization. The Het currents had a larger component of fast desensitization (40 ± 1%) than wild-type currents (30 ± 1%; p < 0.001) (Fig. 3A,B). The Het currents also had a greater total component of desensitization (65 ± 2%) than wild type (51 ± 3%; p < 0.05). The time constants of the fast (1) and intermediate (2) components of desensitization, the component of intermediate desensitization (%A2), and the activation and deactivation times did not significantly differ between wild-type and Het currents (Table 2). There was no significant difference in the slow component of desensitization as measured with 6 sec GABA applications (supplementary Table 2).
Tethered wild-type and Het receptor GABA concentration-response curves were similar
We determined the GABA concentration-response curves for wild-type and Het tethered receptors (Fig. 3E). There was no significant difference between the EC50 values or Hill coefficients of wild-type (42 ± 0.4 µM; 1.3 ± 0.07) and Het (32 ± 0.4 µM; 1.2 ± 0.10) receptors (p > 0.05). Similar to the untethered GABAA receptor, both wild-type and Het receptors had maximal currents at GABA concentrations <1 mM, the GABA concentration that was used in this study to measure both peak currents and rapid current kinetics. The GABA EC50 value of wild-type tethered receptors was somewhat lower than that measured previously (177 µM) in Xenopus oocytes (Baumann et al., 2002).
1(A322D) reduced protein expression of the - construct
We performed Western blots to determine how the 1(A322D) mutation affected protein expression of the tethered constructs. No specific immunoreactive peptides were detected using the monoclonal antibody targeted against the N terminus of the 1 subunit that had been used in the Western blots of the untethered subunits. This result was not surprising because it had been asserted that the anti-1 antibody requires a free N terminus (Baumann et al., 2001). Therefore, the Western blots of the tethered GABAA receptor were probed with a monoclonal antibody directed against the 2 and 3 GABAA receptor subunits. Lysates (30 µg protein) from untransfected HEK293T cells (UT) or HEK293T cells transfected with tethered wild-type (WT), Het (), Het (), or homozygous (Hom) GABAA receptors were analyzed by Western blots and probed with the monoclonal antibody targeted against the 2 subunit. The only specific immunoreactive protein was present at 100 kDa, the theoretical molecular weight of the tethered - tandem construct. In each of the five Western blot experiments (Fig. 4), both visual and quantitative analyses demonstrated that Het transfections had lower expression of the - construct than wild-type transfections (71 ± 9% relative to wild type) but higher expression of the - construct than Het transfections (51 ± 16% relative to wild type). However, because there was substantial variance in the quantification of the - band from the five experiments, the difference between the mean quantified - band from the Het and Het transfections was not statistically significant (p = 0.32). The tethered homozygous mutant receptors had even more reduced expression (36 ± 14% relative to wild type; n = 4) of the - concatamer.
The concatamer immunoblots also demonstrated that there was no immunoreactive protein at 50 kDa, and thus the linker between the and subunits in the tandem construct remained intact. Furthermore, there was also no specifically labeled band at 150 kDa, the theoretical molecular weight of the -- triplet concatamers, suggesting that the monoclonal antibody targeted against the N terminus of the 2 subunit required a free N terminus similar to the antibody against the 1 subunit N terminus. Unfortunately, there are no commercially available monoclonal antibodies targeted against the 2 subunit that would immunoreact with the triplet (--) construct. Incubation of Western blots of tethered or untethered subunits with polyclonal antibodies directed against the N terminus did not reveal any specifically labeled protein.
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Discussion
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Genetic mutation is an important etiological factor in many idiopathic epilepsy syndromes (Annegers et al., 1996). To date, 13 genes have been identified in which mutations are directly associated with human epilepsy (Scheffer and Berkovic, 2003). Because each of these genes is inherited in an autosomal dominant pattern, characterizing GABAA receptor properties with these mutations in a heterozygous expression system is necessary to determine how mutations of these genes cause disease. We characterized the ADJME 1(A322D) mutation in a standard heterozygous expression system, in which all four possible GABAA receptor 1 subunit combinations are likely expressed, as well in a tethered system, in which each position of the 1 subunit in the GABAA receptor could be specifically targeted. Finally, we demonstrated the technical validity of expressing tethered GABAA receptor subunits in a mammalian expression system without degradation of the tether as evidenced by the lack of significant currents when either concatamers was expressed alone as well as by using Western blots, which demonstrated the integrity of the tethered - subunits.
The most prominent consequence of 1(A322D) is the reduction of peak current resulting from decreased 1 subunit expression
The Western blot assays demonstrated that the most important means by which the A322D mutation decreased the mean peak currents in heterozygously and homozygously transfected HEK293T cells was by reducing total and surface 1 subunit. However, it should be emphasized that it is not known whether this inhibition is also present in neurons expressing endogenous mutant 1 subunit-containing receptors. The mechanism by which 1(A322D) reduced 1 protein expression is unknown. It is unlikely that the GCC to GAC mutation reduced the efficiency of translation. In the wild-type 1 subunit, GAC codes 11 of the 23 aspartates, and thus a codon bias against GAC is improbable.
It is possible that 1(A322D) reduced 1 by inhibiting correct GABAA receptor folding and assembly. Our finding that the Het transfections contained less - concatamer than wild-type tethered transfections is consistent with this conclusion. Although the 1(A322D) mutation in the Het transfections is in the -- concatamer, we detected a reduction of the - concatamer. Because GABAA receptors are assembled in the endoplasmic reticulum and incorrectly assembled receptors are degraded (for review, see Barnes, 2000), if --(A322D) reduced the amount of correctly assembled pentamers, both --(A322D) and - would be reduced.
Although many assembly studies identified amino acids at the N termini of the , , and subunits that are important for receptor assembly (Taylor et al., 1999, 2000; Klausberger et al., 2000, 2001a,b; Sarto et al., 2002a,b), recent studies suggest that other domains may also be important. A post-M3 truncation mutant of the 2 subunit caused 2 retention in the endoplasmic reticulum (Harkin et al., 2002). A motif in the M1 transmembrane domain of the nicotinic ACh receptor (AChR), a ligand-gated ion channel that is homologous to the GABAA receptor, is critical for targeting unfolded or misfolded receptors for endoplasmic reticulum degradation (Wang et al., 2002). Furthermore, tryptophan scanning mutagenesis of the AChR M3 transmembrane domain demonstrated that mutation of the interior-facing M3 amino acids, including I283, the homologous residue to GABRA1 1(A322D), substantially reduced surface expression (Guzman et al., 2003).
A second consequence of 1(A322D) is altered channel gating
Although reduction of 1 is likely the most important factor in the diminution of whole-cell peak currents, 1(A322D) also increased the GABA EC50 value and altered whole-cell current kinetics. In addition, single-channel currents from homozygous expression of 1A294D (the homologous mutation in rat GABAA receptors) had substantially altered channel gating; mean open times were reduced from 2.23 to 0.54 msec, and the contribution of the longest open state was reduced from 14.8 to 0.8% (Fisher, 2004). These data demonstrate that 1(A322D) directly alters channel function. This conclusion is consistent with prior structure-function studies of ligand-gated ion channels. Electron microscopic images of the AChR identified a water-filled pocket between the M3 and M2 domains that is likely important for receptor function (Miyazawa et al., 2003). In the GABAA receptor, water-soluble probes of this pocket react with 1 subunit M3 residues near 1A322 only in the presence GABA, suggesting that the M3 domain undergoes an agonist-induced conformational change that is important in signal transduction (Williams and Akabas, 1999). In addition, M3 residues have been found to be important for GABAA receptor interaction by benzodiazepines, ethanol, propofol, and volatile anesthetics, thus demonstrating that this domain is important for GABAA receptor modulation (Krasowski and Harrison, 2000; Williams and Akabas, 2000, 2002; Jenkins et al., 2001). Therefore, it would be expected that a nonconservative amino acid substitution of an alanine with an aspartate might alter the function of the M3 domain.
The 1(A322D) mutation has asymmetrical effects at the two1 subunits
It was of particular interest that the Het receptors differed substantially from the Het receptors. Because the mutant 1 subunit in Het receptors is adjacent to the 2S subunit, the large difference in peak currents between Het and Het receptors may indicate an interaction is needed between 1 M3 and 2S subunits to produce large currents and could explain the relatively small currents produced by GABAA receptors formed from receptors that consist |
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Abstract
Introduction
