National Academies Press: OpenBook

In the Light of Evolution: Volume VI: Brain and Behavior (2013)

Chapter: 2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon

« Previous: 1 Functionalization of a Protosynaptic Gene Expression Network--Cecilia Conaco, Danielle S. Bassett, Hongjun Zhou, Mary Luz Arcila, Sandie M. Degnan, Bernard M. Degnan, and Kenneth S. Kosik
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

This page is blank

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

2

Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years

cth

HAROLD H. ZAKON

Voltage-gated Na+-permeable (Nav) channels form the basis for electrical excitability in animals. Nav channels evolved from Ca2+ channels and were present in the common ancestor of choanoflagellates and animals, although this channel was likely permeable to both Na+ and Ca2+. Thus, like many other neuronal channels and receptors, Nav channels predated neurons. Invertebrates possess two Nav channels (Nav1 and Nav2), whereas vertebrate Nav channels are of the Nav1 family. Approximately 500 Mya in early chordates Nav channels evolved a motif that allowed them to cluster at axon initial segments; 50 million years later with the evolution of myelin, Nav channels “capitalized” on this property and clustered at nodes of Ranvier. The enhancement of conduction velocity along with the evolution of jaws likely made early gnathostomes fierce predators and the dominant vertebrates in the ocean. Later in vertebrate evolution, the Nav channel gene family expanded in parallel in tetrapods and teleosts (~9 to 10 genes in amniotes, 8 in teleosts). This expansion occurred during or after the late Devonian extinction, when teleosts and tetrapods each diversified in their respective habitats, and coincided with an increase in the number of telencephalic nuclei in both groups. The expansion of Nav channels may have allowed for more sophisticated neural computation and tailoring of Nav channel kinetics with potassium channel kinetics to enhance energy savings. Nav channels show adaptive sequence evolution for increasing diversity in communication signals

_______________

Section of Neurobiology, University of Texas, Austin, TX 78712; and Marine Biological Laboratory, The Josephine Bay Paul Center for Comparative Molecular Biology and Evolution, Woods Hole, MA 02543. E-mail: h.zakon@mail.utexas.edu.

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

(electric fish), in protection against lethal Nav channel toxins (snakes, newts, pufferfish, insects), and in specialized habitats (naked mole rats).

Multicellular animals evolved >650 million years ago (Love et al., 2009). The nervous system and muscles evolved shortly thereafter. The phylogeny of basal metazoans is poorly resolved, likely because of the rapid radiation of these then-new life-forms (Rokas et al., 2005), so depending on the phylogeny one embraces, the nervous system evolved once with a loss in sponges, or twice independently in ctenophora and bilateria + cnidaria or bilateria and cnidaria + ctenophora (Moroz, 2009; Schierwater et al., 2009). However, in all animals with nervous systems, neurons generate action potentials (APs), release excitatory and inhibitory neurotransmitters, form circuits, receive sensory input, innervate muscle, and direct behavior.

The history of brain evolution and its key neural genes would fill volumes. I will use voltage-dependent Na+ (Nav, Na-permeable voltage-dependent = protein; scn, sodium channel = gene) channels as an exemplar to tell this story because all neuronal excitability depends on Nav channels, there is a good understanding of their function and regulation from biophysical, biochemical, and modeling studies, and there are fascinating examples of ecologically relevant adaptations. An additional rationale is that although many proteins, such as immunoglobins, sperm and egg receptors, olfactory receptors, opsins, and surface proteins of pathogens, are routinely studied in the field of molecular evolution, only recently have ion channels begun to receive greater attention (Lopreato et al., 2001; Geffeney et al., 2005; Zakon et al., 2006, 2011; Arnegard et al., 2010; Liu et al., 2011); of these studies, the majority are on Nav channels.

SODIUM CHANNEL GENES ARE LATECOMERS TO THE 6TM FAMILY OF VOLTAGE-DEPENDENT ION CHANNELS

Voltage-gated ion channels are the basis of electrical excitability of all animals and many single-celled eukaryotes. Potassium leak and voltage-dependent K+ (Kv) channels appeared 3 billion years ago in bacteria and occur in all organisms (Anderson and Greenberg, 2001) (Fig. 2.1). They establish resting potentials and repolarize membranes after excitatory events. Kv channels are the “founding members” of the family of ion-permeating channels whose basic structure is a protein of six transmembrane helices (6TM) that associate as tetramers to form a channel. At some point early in eukaryote evolution, the gene for a 6TM channel likely duplicated, giving rise to a protein with two domains. These proteins then dimerized to form a complete channel (Strong et al., 1993). Such a channel still exists in the two-pore channel family of Ca2+-permeable channels

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

cth

FIGURE 2.1 Schematic diagram of the evolutionary relationships among some key families in the ion channel superfamily. On the top of the figure is the structure of the channels moving from left to right showing a linear leak K+ channel that is composed of two membrane-spanning helices and a pore (blue), a 6TM channel with a single voltage sensor (red), and four domain 4×6TM channels with four voltage sensors. There is uncertainty about the origin of the 4×6TM family, which more likely evolved in eukaryotes than prokaryotes, as indicated in this figure. A more precise and detailed relationship among Cav and Nav channels in basal metazoans and their sister group, the choanoflagellates, is given in Fig. 2.3. Reprinted from Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 129/1, Peter A. V. Anderson, Robert M. Greenberg, Phylogeny of ion channels: Cues to structure and function, 12-17, Copyright (2001), with permission from Elsevier. [Note: Figure can be viewed in color in the PDF version of this volume on the National Academies Press website, www.nap.edu.]

localized in endosomes and lysozomes (Galione et al., 2009). The gene for a two-domain channel likely duplicated to make a protein with four domains capable of forming a channel on its own (4×6TM). Eventually such a four-domain channel evolved (or retained) permeability to Ca2+, and these handily became involved in intracellular signaling. Other Ca2+-binding proteins and enzymes first appeared in single-celled eukaryotes (Cai, 2008). Additionally, there are single 6TM Na+-permeable channels localized in endosomes and lysozomes (Galione et al., 2009). The gene for a two-domain channel likely duplicated to make a protein with four domains capable of forming a channel on its own (4×6TM). Eventually such a four-domain channel evolved (or retained) permeability to Ca2+, and these handily became involved in intracellular signaling. Other Ca2+-binding proteins and enzymes first appeared in single-celled eukaryotes (Cai, 2008). Additionally, there are single 6TM Na+-permeable channels in

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

bacteria (Koishi et al., 2004). Their relationship to eukaryotic Nav channels is unclear, and they will not be discussed in this review.

The three main types of Cav channels are L, N/P/Q/R, and T. Generally speaking, L-type channels are found in muscle and neuronal dendrites, and N/P/Q/R are found in synaptic terminals and regulate transmitter release, whereas T types, which are sensitive to voltages close to resting potential, underlie spontaneous firing and pacemaking. These three subfamilies appear early in animals in a common ancestor of bilateria and cnidaria (Liebeskind et al., 2011) (Fig. 2.2). Choanoflagellates, single-celled protists that are the sister group to metazoans, and sponges have a single Cav channel gene that is ancestral to the L and N/P/Q/R families. The origin of the T-type channels is not clear.

cth

FIGURE 2.2 Hypothetical secondary structure of a Nav channel. Top: The Nav channel is composed of four repeating domains (I–IV), each of which has six membrane-spanning segments (S1–S6), and their connecting loops (in white). Middle: The four domains cluster around a pore. Bottom: The four P loops dip down into the membrane and line the outer mouth of the channel that is evident in an en face view of a single domain. The black dot represents the single amino acid at the deepest position of each of the four P loops that determines Na+ ion selectivity. From Liebeskind et al. (2011).

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

Nav channels share the 4×6TM structure (Figs. 2.1 and 2.2) with Cav channels, and it has been suggested that Nav channels evolved from Cav channels (Hille, 2001). Analysis of putative Cav and Nav channel genes from fungi, choanoflagellates, and metazoans confirm this speculation and show that choanoflagellates have a channel that groups with recognized Nav channels with strong support (Fig. 2.3). The selectivity filter of 4×6TM channels depends on a single amino acid in each of the four domains that come together and face each other, presumably forming the deepest point in the pore. The selectivity filter of the choanoflagellate and other basal metazoans (DEEA) is midway between bona fide Cav (EEEE) and Nav1 (DEKA) channel pores and lives on in metazoans in a Nav channel found only in invertebrates (Nav2) (Zhou et al., 2004) (Fig. 2.3). This pore sequence and studies of the invertebrate Nav2 suggest that the choanoflagellate Nav channel is likely permeable to both Ca2+ and Na+ and may not be a pure Na+-selective channel. This will be determined when the choanoflagellate Nav channel is expressed and studied in detail.

The presence of a K in domain III of the pore, as in the bilaterian Nav1, increases Na+ selectivity substantially (Fig. 2.3). There is a K in domain II in the Nav channel pore of motile jellyfish (medusozoa) but not in sedentary anemones (anthozoa). The selectivity filter DKEA enhances Na+ selectivity less than DEKA but more than DEEA (Schlief et al., 1996; Lipkind and Fozzard, 2008). The nervous system of jellyfish has clusters of neurons approaching a real central nervous system, whereas that of anemones is more of a nerve net. Thus, enhanced Na+ selectivity occurred in parallel in medusozoan and bilaterian Nav channels along with increasing structural complexity of the nervous system (Liebeskind, 2011).

There is little question as to the adaptive advantage conferred by Na+-selective channels in early animals. It was not only that, with the advent of multicellularity, they fulfilled the need in a newly evolved nervous system for rapid communication across distant parts of organisms, but that they did so by marshalling an ion that was abundant in the ocean and would minimally perturb intracellular Ca2+ levels and, therefore, intracellular signaling (Hille, 2001).

Besides the obvious change from Ca2+ to Na+ permeability, other changes occurred as well. The short intracellular loop between domains III and IV evolved function as the inactivation “ball” (West et al., 1992). In voltage-dependent K+ channels all four voltage sensors must be “engaged” for the channel to open. In the Na+ channel, activation is accomplished by the three voltage sensors in domains I–III; the voltage sensor in domain IV initiates inactivation (Chanda and Bezanilla, 2002; Chanda et al., 2004). No Cav channel has been examined in such a way that we do not know whether they also have equivalently acting voltage sensors or whether the voltage sensor in domain IV had already evolved a novel function.

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

cth

FIGURE 2.3 Maximum likelihood phylogeny of the voltage-gated sodium channel family. The common ancestor of choanoflagellates (represented by Monosiga in green) and animals had a Nav channel that was likely permeable to Ca2+ and Na+ (pore motif = DEEA). This motif is present in the Nav channels of anthozoan cnidaria (anemones, coral) and the Nav2 channel of invertebrates. The presence of a lysine (K) in the pore improves Na+ selectivity (indicated by red star). A lysine is found in the Nav1 channels of bilaterians (DEKA) and Nav channel of medusozoan cnidaria (jellyfish) (DKEA), both of which have more centralized nervous systems than anthozoans and are motile. Additionally, there is strong conservation of a hydrophobic (blue) triplet of amino acids in the “inactivation gate” region. From Liebeskind et al. (2011). [Note: Figure can be viewed in color in the PDF version of this volume on the National Academies Press website, www.nap.edu.]

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

EVOLUTION OF NA+ CHANNEL CLUSTERING AT THE AXON INITIAL SEGMENT AND THE NODES OF RANVIER

Myelination and saltatory conduction are key innovations of the vertebrate nervous system that markedly increase axonal conduction velocity [myelination evolved multiple times in some invertebrate lineages as well despite a widespread and persistent belief to the contrary (Hartline and Colman, 2007; Wilson and Hartline, 2011)]. Myelination is not present in agnathans but occurs in all gnathostomes, likely appearing first in a placoderm ancestor (Zalc et al., 2008). Saltatory conduction depends on high densities of Nav channels at the nodes of Ranvier that inject sufficient current into the axon to depolarize the adjacent node to threshold. KCNQ-type K+ channels, which help to repolarize the AP, cluster at nodes as well, both channels tethered to ankyrin and thence to the cytoskeleton.

Remarkably, both Nav and KCNQ K+ channels evolved the same specific nine-amino acid motif for ankyrin binding (Hill et al., 2008). This motif first appears in the Nav channels of ascidians and agnathans and, indeed, Nav channels cluster at axon initial segments (AIS) in the lamprey. In lampreys, and presumably nonvertebrate chordates, the high-density clustering of Nav channels adjacent to the soma ensures sufficient current injection into the high-resistance axon in the face of current shunting by the low-resistance soma (Kole et al., 2008). Shiverer mice, which have a mutation that prevents the formation of compact myelin, retain a high density of Nav channels (Nav1.6) at the AIS but not along the axon (Boiko et al., 2003). This emphasizes the distinction between older non–myelin-dependent mechanisms for clustering Nav channels at the AIS and more recent myelin-dependent clustering of Nav channels at nodes. A surprising observation is that the AIS is mobile, moving toward the soma when a neuron’s firing rate is low and away from the soma when it is high (Grubb and Burrone, 2010). This is likely different from the nodes of Ranvier, which are smaller and constrained by the myelin sheath. However, this remains to be investigated.

KCNQ channels only occur in gnathostomes. Once KCNQ channels appeared, all of the molecular components for construction of the nodes of Ranvier were in place. By this time the key genes for myelin components had also evolved (Schweigreiter et al., 2006; Li and Richardson, 2008).

MAKING UP FOR LOST TIME: VERTEBRATE NAV CHANNEL GENES DUPLICATED EXTENSIVELY IN TELEOSTS AND TETRAPODS

Invertebrates have two Nav channel genes, Nav1 and Nav2, each in single copy. We have little information on the normal physiological role of

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

Nav2 channels in invertebrates [knockouts in Drosophila are not lethal and produce only a mild phenotype (Stern et al., 1990; Kulkarni et al., 2002)]. It is interesting that both genes have been lost in nematodes (Bargmann, 1998), most of which are small and depend on passive transmission of electrical activity. The predominant Nav channel gene in invertebrates (para in Drosophila), and the only Nav channel gene in vertebrates, is Nav1. However, Nav1 has duplicated in vertebrates.

In a prescient insight in 1970, Susumu Ohno suggested that vertebrates underwent two rounds of whole-genome duplication (WGD) at their origin (2R hypothesis) and that a subsequent third WGD occurred in teleost fishes (3R) (Ohno, 1970). Ohno believed that these ploidy events provided the raw genetic material from which emerged many of the defining features of vertebrates. Although originally controversial, his view has been empirically confirmed (Meyer and Schartl, 1999; Jaillon et al., 2004). Nav1 channel genes show a perfect read-out of this history. A single Nav1 channel gene is present in tunicates, two in lampreys, four in elasmobranchs and in the common ancestor of teleosts and tetrapods (Lopreato et al., 2001; Novak et al., 2006; Widmark et al., 2011; Zakon et al., 2011). As expected from a teleost-specific WGD, eight Nav channel genes are found in teleosts (Fig. 2.4).

However, further gene duplication/retention occurred in tetrapods above and beyond that predicted by 2R. Two of the four Nav channel genes of our tetrapod ancestors underwent a series of tandem duplications in early amniotes, so that the stem reptilian ancestor of modern-day reptiles, birds, and mammals had nine Nav1 channel genes (Widmark et al., 2011; Zakon et al., 2011). A final duplication occurred early in the mammalian lineage, giving us 10 Nav channel genes.

Was the retention of these duplicate genes in tetrapods adaptive? We can approach this by comparing the fates of Nav channel genes with other genes in tetrapods throughout 2R and beyond. In tetrapods, the genes surrounding the Nav channel genes that would have duplicated along with them in 2R show little or no evidence of further duplication and retention; indeed, some show a loss of one or more 2R duplicates (Fig. 2.4). This pattern of duplication and retention of Nav channel genes is statistically significantly different compared with that of the immediately surrounding genes (Zakon et al., 2011). A similar analysis in teleosts shows that nearby genes, such as members of the TGF-β receptor superfamily, were also more likely to be lost than retained (Widmark et al., 2011). Furthermore, an analysis of Cav, transient receptor potential, and various K+ channel subfamilies shows that there was no widespread duplication and retention of other ion channel genes in the tetrapod 6TM family since the teleost–tetrapod divergence (Zakon et al., 2011). Thus, we infer that selection acted on the Nav channel duplicates independently in teleosts

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

cth

FIGURE 2.4 The Nav channel gene family underwent an expansion in parallel in teleosts and tetrapods. (A) A schematic chromosome with Nav channel genes (SCN, sodium channel) surrounded by other genes. (B) This chromosome, along with all of the other ancestral chordate chromosomes, duplicated twice at the origin of vertebrates (2R). (C) There was an additional round of genome duplication in teleosts (3R) and (D) tandem duplications of Nav channel genes in ancestral tetrapods and amniotes. There is no indication of any loss of Nav channel genes despite losses of surrounding genes in both teleosts and tetrapods. Furthermore, although not shown here, no other ion channel gene family duplicated after the teleost and tetrapod divergence. Thus, there was likely to be strong selection for the preservation of Nav channel gene duplicates. Reprinted from Jenny Widmark, Görel Sundström, Daniel Ocampo Daza, Dan Larhammar, Differential evolution of voltage-gated sodium channels in tetrapods and teleost fishes, Molecular Biology and Evolution, 2011, by permission of Oxford University Press. [Note: Figure can be viewed in color in the PDF version of this volume on the National Academies Press website, www.nap.edu.]

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

cth

FIGURE 2.5 Nav1.4a is a fast-evolving Nav channel expressed in the electric organs of two independently derived lineages of weakly electric fish. Two paralogous genes, (A) scn4aa, which encodes Nav1.4a, and (B) scn4ab, which encodes Nav1.4ab, are expressed in the muscles of teleost fish. In the two lineages of weakly electric fishes, the mormyroidea and gymnotiformes, the gene for Nav1.4a (scn4aa) lost its expression in muscle and is only expressed in the electric organ. Nav1.4a underwent a burst of accelerated evolution at the origin of each lineage of electric fish. Nav1.4b, which is expressed in muscle and may also be expressed in the electric organ, evolved at a lower rate. The rate of nonsynonymous substitutions/nonsynonymous sites/rate of synonymous substitutions/synonymous site (dN/dS) in each gene is shown by a color scale in which cool colors represent

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

and tetrapods to preserve them. Future work detailing where Nav channels are expressed and how they behave in ray-finned fish, lungfish, and nonmammalian tetrapods will shed light on this question.

The addition of new Nav channels to the existing repertoire likely realized two benefits: enhanced computational ability and increased energetic efficiency. For example, Nav1.1 is expressed in fast-firing inhibitory cortical interneurons, and its properties allow these neurons to fire at sustained high rates (Ogiwara et al., 2007). In pyramidal neurons, Nav1.6 is found in the distal part of the AIS, whereas Nav1.2, which activates at voltages around 20 mV more positive than Nav1.6, is found more proximally. This will ensure that APs that are first generated in the most distal AIS propagate down the axon and these are followed by APs generated in the proximal AIS that backpropagate into the soma (Hu et al., 2009).

The extent to which Na+ channels inactivate before K+ currents commence influences energy consumption; optimally Nav channels should completely inactivate before the K+ channels open to minimize use of the ATP-dependent Na+/K+ pump (Hasenstaub et al., 2010; Schmidt-Hieber and Bischofberger, 2010; Sengupta et al., 2010). It is possible that variation in the properties of Nav channels allows more precision in matching their inactivation with Kv channels to save energy.

ADAPTIVE EVOLUTION OF NAV CHANNELS: WEAKLY ELECTRIC FISH

In most organisms ion channels cause behavior indirectly by triggering muscle movements. Weakly electric fish, however, emit electric signals directly into the water, and these are shaped by the biophysical properties of Nav and Kv channels in their electric organs. In nonteleost vertebrates the Nav channel Nav1.4 is expressed in muscle; because of the teleost-specific WGD, teleosts have two paralogs, Nav1.4a and Nav1.4b, in their muscles (Zakon et al., 2006; Arnegard et al., 2010) (Fig. 2.5). There must

low rates of sequence evolution and hot colors represent high rates. The arrows indicate where Nav1.4a gene expression was lost from muscle in both lineages. The production of either a highly regular wave type or an irregular pulse type of electric organ discharge is indicated in both groups. In both lineages of electric fishes, the electric organ develops from muscle (myogenic), except for one group (Apteronotidae) in which it is derived from the axons of motorneurons. From Arnegard et al. (2010). [Note: Figure can be viewed in color in the PDF version of this volume on the National Academies Press website, www.nap.edu.]

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

be strong selection for the retention of the expression of both paralogs in muscle because they are both expressed in muscles of most teleosts examined. In other words, the expression of both genes in fish muscle remains after 250 million years of teleost history. The only exceptions are two lineages of weakly electric fishes. These two groups—the South American gymnotiforms and African mormyriforms—evolved electric organs independently. In both lineages the gene for Nav1.4a (scn4aa) lost its expression in muscle and became compartmentalized in the electric organ. Nav1.4 in mammals is under strong purifying selection because mutations in the gene for this channel often cause muscle paralysis or myotonia. Freed from its constraints, Nav1.4a underwent a burst of evolutionary change at the origin of both groups of electric fishes, with numerous substitutions in key regions of the channel, many involved in inactivation (Zakon et al., 2006; Arnegard et al., 2010). The pace of evolutionary change quickened in similar regions of the channel in both groups; in some cases the same or neighboring amino acids changed in both groups. Although these substitutions have not yet been introduced into a channel and their effects tested, the implication is that these substitutions have facilitated the diversity of species-specific signals in these fish. An unanswered question is this: if nonelectric teleosts need two Nav channel paralogs, how do electric fish cope with only a single channel?

Muscles have diversified in other lineages of fishes. For example, rapidly contracting sound-producing muscles evolved independently in at least three lineages of fishes (Bass and Ladich, 2008), and heater muscles that no longer contract but that engage in futile Ca2+ cycling to generate heat, in two lineages (Block et al., 1993). It would be intriguing to know whether Nav channels show a similar pattern of compartmentalized expression and rapid evolutionary change in specialized muscles and muscle-derived organs of these lineages. Has the duplication of a muscle-expressing Nav channel gene facilitated the evolution of multiple novel muscle-derived structures in teleosts?

ADAPTIVE EVOLUTION OF NAV CHANNELS: TETRODOTOXIN RESISTANCE

The best-studied cases of adaptive evolution of Nav channel genes involve the evolution of resistance to the various neurotoxins that act on Nav channels. A number of animals use the neurotoxin tetrodotoxin (TTX), mainly for protection against predators (Gladstone, 1987) but in a few cases as a weapon to subdue prey (Ritson-Williams et al., 2006). Animals associated with TTX span the animal kingdom. This is because TTX is likely produced by bacteria symbiotically associated with their hosts, or else taken up from the food chain by animals that prey on TTX-accumulating

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

organisms (Lee et al., 2000). In any event, unlike peptide toxins that are sequestered within a gland, TTX passes through cell membranes so that although it may be concentrated in certain tissues, all tissues are more or less exposed to it (Williams and Caldwell, 2009). Thus, those animals that sequester high concentrations of TTX have evolved mechanisms to protect themselves from its effects (Kidokoro et al., 1974; Flachsenberger and Kerr, 1985). Because invertebrates possess only a single Nav channel gene, TTX resistance could occur easily enough with a single amino acid substitution. However, TTX resistance in vertebrates is more complex because vertebrates have multiple Nav channel genes. Evolution of TTX resistance in vertebrates offers an interesting case of parallel molecular evolution.

Pufferfishes, the most famous being the culinary delicacy Fugu of Japan, sequester TTX. This is a general trait of tetraodontiform fishes of which there are more than 120 species. Sequencing of Nav channel genes from Fugu and other pufferfishes shows that many of the same TTX-resistant amino acid substitutions have occurred multiple times in various Nav channels and lineages of pufferfishes (Yotsu-Yamashita et al., 2000; Venkatesh et al., 2005; Jost et al., 2008). We still do not know how pufferfish were able to survive with only one or a few TTX-resistant Nav channels. The most likely scenario is that TTX-resistant mutations accumulated gradually in the Nav channel genes as fish were initially exposed to a light load of TTX. Gradually, as more channels gained resistance, they were able to carry a greater toxic load. This is suggested by the fact that certain substitutions were present in ancestral tetraodontids, with other substitutions appearing in different lineages of pufferfish and in different Nav channels (Jost et al., 2008).

Some of the most remarkable work in this field concerns the rich and extensively studied garter snake–newt system. Newts such as the California newt (Taricha torosa) sequester high levels of TTX for protection against predators. However, in some regions in the Pacific Northwest and northern California, the common garter snake (Thamnopis sirtalis) overlaps with some populations of the newt. Garter snakes that do not overlap with the newts are severely affected by ingesting newts and will vomit up the newt if they are lucky and die if they are not. However, populations of garter snakes sympatric with the newts are resistant to TTX and handily take newts. Variation in the extent of TTX resistance in different garter snake populations suggests that each population has evolved resistance independently. Even more striking, TTX resistance has evolved multiple times in populations of other species of garter snakes that are also sympatric with Taricha in the Pacific Northwest and California, as well as other snake species sympatric with other newts or frogs that use TTX in South America and Asia (Feldman et al., 2009, 2012). Finally, sequencing and testing of expressed Nav channels (Nav1.4, a muscle-expressing Nav

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

channel encoded by the scn4a gene) have highlighted that these channels show amino acid substitutions in the pore where TTX binds (Geffeney et al., 2005; Feldman et al., 2012). Not surprisingly, the Nav channels of the newts also have evolved TTX resistance to keep the newts from poisoning themselves (Kaneko et al., 1997).

However, this story is richer still. Newts lay their eggs in streams and ponds, and these eggs hatch into gill-bearing larvae. The larvae do not produce much TTX. Adults, however, do. The adults are carnivorous and may be cannibalistic. Larval newts that are “downwind” of adults will flee if they smell TTX wafting toward them in the water (Zimmer and Ferrer, 2007). Thus, TTX is used as a chemical signal [it is similarly used as an attractive pheromone in pufferfish, in which males can detect nanomolar levels of TTX that diffuse into the water from the TTX that females place in their eggs (Matsumura, 1995)]. It is not known yet what receptor detects the TTX in either newts or pufferfish. One possibility is that it is a Nav channel that has evolved to open, rather than close, upon TTX binding.

Newt eggs are protected from most vertebrate predators because of their high titer of TTX. Nevertheless, caddis fly (Limnephilus flavastellus) larvae have evolved TTX resistance and will eat newt eggs (Gall and Brodie, 2011). It is not yet known whether this is due to a substitution in the pore of the Nav channel. Given that invertebrates have only a single Nav channel gene, this seems likely, and it will be interesting to see whether other invertebrate egg-predators are resistant to TTX.

ADAPTIVE EVOLUTION OF NAV CHANNELS: PROTON INSENSITIVITY

Naked mole rats (Heterocephalus glaber) live at high density in subterranean tunnels and seldom emerge into the light. They have evolved a number of adaptations for this life history, among them insensitivity to acid (Park et al., 2008). The levels of CO2 that build up in their tunnels make carbonic acid; humans exposed to these levels of CO2 report stinging pain. However, naked mole rats show no pain-related behaviors and their C-fiber nociceptors are not activated by acid. Molecular and physiological examination of the naked mole rat’s acid-sensing (ASIC) and transient receptor V1 (TRPV1) channels, the channels in vertebrates that subserve acid sensitivity, showed no unusual behavior in these animals. Insofar as protons are also small monovalently positively charged molecules, these interact with and block Na+ channels. The Nav channel Nav1.7 sets the threshold for firing of C-fiber nociceptors. Naked mole rat Nav1.7, indeed, is extremely sensitive to proton block, ensuring that, at low pH, Nav1.7 will be blocked and the C-fiber nociceptors are not activated (Smith et al., 2011).

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×

ADAPTIVE EVOLUTION OF NAV CHANNELS IN REAL TIME: INSECTICIDE RESISTANCE

One unintended consequence of the liberal and worldwide use of dichlorodiphenyltrichloroethane, pyrethrin, and pyrethroid insecticides has been the rapid, massively parallel evolution of resistance to these pesticides in insects (Taylor et al., 1993; Liu et al., 2000; Davies et al., 2007; Jones et al., 2012). Starting with their use in the 1940s, the first indications of resistance, so-called knockdown resistance because insects were no longer knocked down by normal concentrations of the insecticide, were evident in the early 1950s. These insecticides target the Nav1 channels of insects. They cross the cell membrane and lodge in a hydrophobic pocket in the inner mouth of the channel, where they are believed to prevent the inactivation gate (domain III–IV linker) from occluding the inner mouth of the channel. This allows Na+ ions to continue flowing into the cell, causing hyperexcitabiity. Amino acid substitutions have been discovered in a variety of insects at a number of sites in the inner mouth of the insect Nav channel (para in Drosophila) that either reduce pesticide binding or alter the channel properties to counteract the effects of insecticides. An example of the latter is a substitution that causes the channel to open at more positive potentials and to enhance the rate at which Nav channels enter closed-state inactivation. This minimizes the number of open channels counteracting the prolonged channel opening caused by insecticides.

The rapid evolution of Nav channels in insects exposed to insecticides is one of many warnings we have about the robust abilities of insect pests to overcome our best attempts to wipe them out.

CONCLUSIONS AND FUTURE DIRECTIONS

Like many key components of the nervous system, Nav channels existed before neurons. It is likely that the Nav channels of choanoflagellates and early metazoans were permeable to both Na+ and Ca2+ and evolved enhanced selectivity to Na+ in parallel in early bilaterians and jellyfish. Although it is convenient to think that invertebrates possess only a single Nav1 channel gene, it is worth scouring the wealth of new genomes to determine whether there are any lineage-specific duplications, and if so, what this might mean. Further, we have little information on the Nav2 channels of invertebrates.

The parallel expansion of Nav channel genes in tetrapods and teleosts occurred along with an increase in the number of telencephalic nuclei in both groups. This was coincident with or just after the great Devonian extinction, during which teleosts began their domination of the aquatic and tetrapods of the terrestrial habitats. More types of Nav channels may allow for more sophisticated computational possibilities and energy savings.

Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 21
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 22
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 23
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 24
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 25
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 26
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 27
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 28
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 29
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 30
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 31
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 32
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 33
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 34
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 35
Suggested Citation:"2 Adaptive Evolution of Voltage-Gated Sodium Channels: The First 800 Million Years--Harold H. Zakon." National Academy of Sciences. 2013. In the Light of Evolution: Volume VI: Brain and Behavior. Washington, DC: The National Academies Press. doi: 10.17226/13462.
×
Page 36
Next: 3 Evolution of Centralized Nervous Systems: Two Schools of Evolutionary Thought--R. Glenn Northcutt »
In the Light of Evolution: Volume VI: Brain and Behavior Get This Book
×
Buy Hardback | $69.00 Buy Ebook | $54.99
MyNAP members save 10% online.
Login or Register to save!
Download Free PDF

The central goal of the In the Light of Evolution (ILE) series is to promote the evolutionary sciences through state-of-the-art colloquia--in the series of Arthur M. Sackler colloquia sponsored by the National Academy of Sciences--and their published proceedings. Each installment explores evolutionary perspectives on a particular biological topic that is scientifically intriguing but also has special relevance to contemporary societal issues or challenges.

This book is the outgrowth of the Arthur M. Sackler Colloquium "Brain and Behavior," which was sponsored by the National Academy of Sciences on January 20-21, 2012, at the Academy's Arnold and Mabel Beckman Center in Irvine, CA. It is the sixth in a series of Colloquia under the general title "In the Light of Evolution." Specifically, In Light of Evolution: Brain and Behavior focuses on the field of evolutionary neuroscience that now includes a vast array of different approaches, data types, and species.

This volume is also available for purchase with the In the Light of Evolution six-volume set.

  1. ×

    Welcome to OpenBook!

    You're looking at OpenBook, NAP.edu's online reading room since 1999. Based on feedback from you, our users, we've made some improvements that make it easier than ever to read thousands of publications on our website.

    Do you want to take a quick tour of the OpenBook's features?

    No Thanks Take a Tour »
  2. ×

    Show this book's table of contents, where you can jump to any chapter by name.

    « Back Next »
  3. ×

    ...or use these buttons to go back to the previous chapter or skip to the next one.

    « Back Next »
  4. ×

    Jump up to the previous page or down to the next one. Also, you can type in a page number and press Enter to go directly to that page in the book.

    « Back Next »
  5. ×

    Switch between the Original Pages, where you can read the report as it appeared in print, and Text Pages for the web version, where you can highlight and search the text.

    « Back Next »
  6. ×

    To search the entire text of this book, type in your search term here and press Enter.

    « Back Next »
  7. ×

    Share a link to this book page on your preferred social network or via email.

    « Back Next »
  8. ×

    View our suggested citation for this chapter.

    « Back Next »
  9. ×

    Ready to take your reading offline? Click here to buy this book in print or download it as a free PDF, if available.

    « Back Next »
Stay Connected!