Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3.3 channels
© Mock et al. 2010
Received: 20 March 2010
Accepted: 16 August 2010
Published: 16 August 2010
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© Mock et al. 2010
Received: 20 March 2010
Accepted: 16 August 2010
Published: 16 August 2010
The zebrafish has been suggested as a model system for studying human diseases that affect nervous system function and motor output. However, few of the ion channels that control neuronal activity in zebrafish have been characterized. Here, we have identified zebrafish orthologs of voltage-dependent Kv3 (KCNC) K+ channels. Kv3 channels have specialized gating properties that facilitate high-frequency, repetitive firing in fast-spiking neurons. Mutations in human Kv3.3 cause spinocerebellar ataxia type 13 (SCA13), an autosomal dominant genetic disease that exists in distinct neurodevelopmental and neurodegenerative forms. To assess the potential usefulness of the zebrafish as a model system for SCA13, we have characterized the functional properties of zebrafish Kv3.3 channels with and without mutations analogous to those that cause SCA13.
The zebrafish genome (release Zv8) contains six Kv3 family members including two Kv3.1 genes (kcnc1a and kcnc1b), one Kv3.2 gene (kcnc2), two Kv3.3 genes (kcnc3a and kcnc3b), and one Kv3.4 gene (kcnc4). Both Kv3.3 genes are expressed during early development. Zebrafish Kv3.3 channels exhibit strong functional and structural homology with mammalian Kv3.3 channels. Zebrafish Kv3.3 activates over a depolarized voltage range and deactivates rapidly. An amino-terminal extension mediates fast, N-type inactivation. The kcnc3a gene is alternatively spliced, generating variant carboxyl-terminal sequences. The R335H mutation in the S4 transmembrane segment, analogous to the SCA13 mutation R420H, eliminates functional expression. When co-expressed with wild type, R335H subunits suppress Kv3.3 activity by a dominant negative mechanism. The F363L mutation in the S5 transmembrane segment, analogous to the SCA13 mutation F448L, alters channel gating. F363L shifts the voltage range for activation in the hyperpolarized direction and dramatically slows deactivation.
The functional properties of zebrafish Kv3.3 channels are consistent with a role in facilitating fast, repetitive firing of action potentials in neurons. The functional effects of SCA13 mutations are well conserved between human and zebrafish Kv3.3 channels. The high degree of homology between human and zebrafish Kv3.3 channels suggests that the zebrafish will be a useful model system for studying pathogenic mechanisms in SCA13.
Voltage-dependent Kv3 K+ channels have specialized gating properties, including a depolarized activation range, fast activation, and very fast deactivation, that facilitate rapid, repetitive firing in neurons [1, 2]. In mammals, there are four Kv3 genes, KCNC1-KCNC4, which encode Kv3.1-Kv3.4 . Each gene is alternatively spliced, generating channel proteins with different carboxyl-terminal sequences . Kv3.3 and Kv3.4 contain amino-terminal extensions that mediate N-type ball-and-chain inactivation .
Recently, KCNC3, which encodes Kv3.3, was identified as the gene mutated in spinocerebellar ataxia type 13 (SCA13) [4, 5]. The spinocerebellar ataxias are a group of 28 human autosomal dominant genetic diseases characterized by motor deficits, eye movement abnormalities, and degeneration of cerebellar neurons [6, 7]. SCA13 is the first neurodegenerative disease known to be caused by mutations in a K+ channel gene .
The two originally-identified SCA13 mutations lead to distinct clinical manifestations that are likely caused by their differential effects on Kv3.3 function . The R420H mutation is associated with adult onset, progressive ataxia accompanied by progressive cerebellar degeneration. R420H is located in the S4 transmembrane segment, the main functional element of the voltage sensor. This mutation suppresses the amplitude of Kv3 currents by a dominant negative mechanism . In contrast, the F448L mutation is associated with persistent motor deficits that emerge in infancy. In affected children, the cerebellum is severely shrunken and malformed . F448L is located near the cytoplasmic end of the S5 transmembrane segment, a region of the protein that couples voltage sensor conformational changes to opening and closing of the pore . This mutation affects the unique gating properties of Kv3 channels, shifting the voltage dependence of pore opening in the hyperpolarized direction and dramatically slowing channel closure . Interestingly, F448L changes a phenylalanine residue found only in Kv3 channels to leucine, the residue found at the analogous position in all other Kv channel subfamilies . As a result, the mutation confers Shaker-like gating properties on Kv3.3 . The distinct clinical manifestations of the R420H and F448L mutations are not likely to result from differences in genetic background because there is a strong genotype/phenotype correlation for age of disease onset in unrelated SCA13 families .
Kv3.3 is prominently expressed in cerebellar neurons [10, 11]. Given the importance of Kv3 channels in controlling neuronal firing patterns, the locomotor deficits and loss of cerebellar neurons seen in SCA13 may result from changes in the excitability of Kv3.3-expressing cells. Development of an animal model is essential to investigate the mechanistic basis of SCA13 and to explore the connections between electrical excitability, control of locomotor behavior, and neuronal cell death.
In recent years, the zebrafish, Danio rerio, has been used extensively to investigate neuronal development. In addition, work from a growing number of laboratories demonstrates that zebrafish has great potential for analyzing nervous system function [12–16]. The zebrafish has been suggested as a model system for studying diseases that affect neuronal function and locomotion [17–19]. As the first step in assessing the suitability of zebrafish as a model system for SCA13, we have identified Kv3 family members in zebrafish and characterized the functional properties of wild type and mutant Kv3.3 channels.
We report that the zebrafish genome (Zv8) encodes six Kv3 family members including two Kv3.3 genes, kcnc3a and kcnc3b. Zebrafish and mammalian Kv3.3 channels exhibit strong functional homology and are similarly affected by SCA13 mutations. These results suggest that the zebrafish is a promising model system for investigating the pathogenic mechanisms underlying SCA13.
Genomic locations of Kv3 family orthologs in zebrafish genome (Zv8)
N-term. Exon 2
S1-S6 Exon 2
Prox. C-term. Exon 2
Distal C Exon 2
Alt. C Exon 2
To assemble putative sequences for Kv3 proteins in zebrafish, predicted coding exons were identified directly by sequence similarity to the mammalian Kv3 proteins. Exons encoding the amino terminus, transmembrane core domain, and proximal carboxyl terminus were found at each of the six genomic locations (Table 1). Many of these exons were also recognized by Ensembl transcript identification algorithms. In addition, each location contained one or more exons encoding the distal carboxyl terminus, a region that is alternatively spliced in mammalian Kv3 genes (Table 1).
According to the Zv8 genome release, plausible Kv3 genes were located at five of the six identified genomic locations. Putative coding exons were encoded on a single strand and were located in the correct order along the chromosome (Table 1). In contrast, the Kv3.3 gene on chromosome 24, kcnc3b, was rearranged (Table 1). Because the genome assembly is preliminary, this does not preclude the presence of an intact Kv3.3 gene on chromosome 24.
Alternative splicing of the carboxyl terminus had no significant effect on channel function (Fig. 6B, C). Similarly, alternative splicing of mammalian Kv3 genes does not alter the functional properties of the channel [1, 27]. Instead, different Kv3 carboxyl termini may be involved in targeting channel proteins to different subcellular compartments .
Zebrafish Kv3.3 currents showed prominent inactivation (Fig. 6A, C). Zebrafish channels inactivated more quickly than human Kv3.3 (data not shown), presumably because the amino terminal extension is shorter in the fish protein (Additional file 1, Fig. S1; Fig. 5) . Deleting the amino terminal extension removed fast inactivation, indicating that zebrafish Kv3.3, like mammalian Kv3.3 channels, is subject to N-type ball and chain inactivation (Fig. 6D) [1, 28]. Co-expression of the non-inactivating zebrafish Kv3.3 with wild type human Kv3.3 produced currents with intermediate inactivation kinetics, consistent with co-assembly of the human and zebrafish subunits into functional tetrameric channels, as expected (data not shown) .
Similarly to the human mutation, F363L dramatically slowed channel deactivation (Fig. 10C). Tail currents, evoked in an 89 mM Rb+ bath solution by repolarizing the membrane from +40 to -90 mV, were fitted with a single exponential function to characterize deactivation kinetics (Fig. 10D). Values of τdeact in wild type Kv3.3 and the F363L mutant were 1.8 ms and 23.3 ms, respectively. Thus, F363L slowed channel closing by ~13-fold at -90 mV. For comparision, the analogous mutation in human Kv3.3 (F448L) slowed channel closing by ~7-fold at -90 mV . Therefore, like its human counterpart, the F363L mutation specifically affects the voltage dependence of activation and the kinetics of channel closing, converting the unique Kv3 gating properties to more closely resemble those of a Shaker-type channel . Our results demonstrate that SCA13 mutations have similar effects on human and zebrafish Kv3.3 channels, confirming that there is strong functional homology between Kv3.3 in teleost and mammalian species .
Genes encoding the voltage-dependent Kv3.1, Kv3.2, Kv3.3, and Kv3.4 K+ channels have been identified in the zebrafish, Danio rerio. Two paralogous genes exist for both Kv3.1 and Kv3.3, reflecting an ancient genome duplication in the teleost line during evolution . The unique gating properties of Kv3 channels are conserved in zebrafish Kv3.3, suggesting that Kv3 channels play an essential role in facilitating fast spiking in zebrafish neurons. SCA13 mutations have very similar effects on the activity of human and zebrafish Kv3.3 channels, indicating that the mutations affect fundamental channel properties that have been conserved during evolution. Our results suggest that expressing SCA13 mutant subunits in zebrafish will provide an animal model useful for investigating the cellular basis of SCA13.
The current Ensembl genome release (Zv8) was probed with mammalian Kv3 sequences using Tblastn to identify coding exons, which were assembled and translated. Sequences were aligned with the sequences of Kv3 family members from mammalian, amphibian, and teleost species using the program Muscle v3.7 and the alignment was manually adjusted (Additional file 1, Fig. S1) [20, 21]. A phlyogenetic tree was constructed with the program PhyML using 100 bootstrapping replicates and the Jones, Taylor, Thornton amino acid substitution model [22, 23]. Synteny was evaluated for each Kv3 family member using the program Synteny Database with zebrafish (release Zv8) as the source genome, mouse (release m37) as the outgroup, and a sliding window size of 100 genes [24, 25]. This program is designed for analyzing genomes that have undergone complete duplication during evolution. It identifies pairwise clusters of orthologs and paralogs simultaneously.
Full length kcnc3a cDNA clones with the WIKP or PSIL alternatively spliced carboxyl termini were cloned by RT-PCR using gene specific primers designed from Zv8 genomic sequences (Fig. 4D). Amplified sequences were inserted into Bluescript. Mutations were generated in the WIKP splice variant using the QuikChange method (Stratagene, La Jolla, CA). Mutations were verified by sequencing. Linearized plasmid DNA was transcribed using the mMessage mMachine T7 or T7 Ultra kit (Ambion, Austin, TX). RNA for each splice variant was separately injected into Xenopus oocytes using standard methods [31, 32].
One to two days after RNA injection, ionic currents were recorded at room temperature (20-22°C) using a Warner OC-725C two electrode voltage clamp [31, 32]. Electrodes were filled with 3 M KCl and had resistances of 0.3-1.0 MΩ. Oocytes were bathed in 85 mM NaCl, 4 mM KCl, 1.8 mM CaCl2, 10 mM HEPES, pH 7.2. To record tail currents, 85 mM NaCl +4 mM KCl was replaced by 89 mM RbCl. Pulse protocols were generated and data were acquired using pClamp software (Axon Instruments, Foster City, CA). Data were sampled at 10 kHz and filtered at 2 kHz using an 8-pole Bessel filter (Frequency Devices, Haverhill, MA). Linear capacitive and leak currents were subtracted using a P/-4 protocol .
Currents were evoked by pulsing from a holding potential of -90 mV to voltages ranging from -80 mV to +60 mV in 10 mV increments. The probability of channel opening as a function of voltage was determined from isochronal tail current amplitudes. Tail current amplitudes were normalized by the maximum value obtained in the experiment and plotted versus voltage. Data were fitted with a single Boltzmann function to determine values for the midpoint potential (V1/2) and slope factor. Deactivation kinetics were measured from tail currents evoked by pulsing to +40 mV before repolarizing to -90 mV. Tail currents were fitted with a single exponential function to obtain values for the deactivation time constant (τdeact).
spinocerebellar ataxia type 13
reverse transcriptase-polymerase chain reaction
We are grateful to Drs. David Glanzman, Joanna Jen, Alvaro Sagasti, Nancy Wayne, Meng-chin Lin and members of the Papazian lab for comments on the work. We thank Drs. Patricia Johnson and Richard Hayes for advice and assistance concerning phylogenetic analysis, and Dr. Hui Sun for providing a zebrafish adult retinal cDNA library. Drs. Alvaro Sagasti, Joanna Jen, Nancy Wayne, Ji-Jun Wan and Scott Henderson generously provided helpful suggestions and assistance. We gratefully acknowledge the help of Yuan Dong of the UCLA Zebrafish Core Facility. This work was supported by NIH grant NS058500 to DMP.
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