Jegla T, Salkoff L
Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, Missouri 63110.
Soc Gen Physiol Ser. 1994;49:213-22.
Cnidarians and ciliate protozoans represent evolutionary interesting phylogenetic groups for the study of K+ channel evolution. Cnidaria is a primitive metazoan phylum consisting of simple diploblast organisms which have few tissue types such as jellyfish, hydra, sea anemones, and corals. Their divergence from the rest of the metazoan line may predate the radiation of the major triploblast phyla by several hundred million years (Morris, 1993). Cnidarians are the most primitive metazoans to have an organized nervous system. Thus, comparing K+ channels cloned from cnidarians to those cloned from more advanced metazoans may reveal which types of K+ channel are most fundamental to electrical excitability in the nervous system. In contrast, channels in ciliate protozoans such as Paramecium may not have been designed to send electrical signals between cells, but simply to control the behavior, such as an avoidance reaction, of a single cell. Hence, comparing cloned Paramecium K+ channels to K+ channels cloned from cnidarians and other metazoans may reveal which types of K+ channel are most fundamental to electrical excitability in eukaryotes, and which K+ channels are specialized for neuronal signaling. Potassium channels are involved in a diversity of tasks and are universally present in eukaryotes. K+ channels set the resting membrane potentials of most metazoan and protozoan cells and are fundamental components of membrane electrical activity in virtually all eukaryotic systems. These channels control the shape, duration and frequency of metazoan action potentials and are known to participate in the action potentials of protozoans, fungi and plants as well (Hille, 1992). Voltage-clamp recordings have shown that a various assortment of voltage-gated K+ channels as well as Ca(2+)-activated K+ channels are widespread in eukaryotes (Hille, 1992). Thus, K+ channels appear to be crucial to behavioral responses in all classes of eukaryotes, including locomotion in metazoans and protozoans, and rapid growth responses and cell shape changes in plants. K+ channel diversity is by far the greatest in metazoans, which have made a strong commitment to electrically excitable cellular networks. There is an apparent need for a great diversity of K+ channel subtypes in these metazoans. Over 50 K+ channel sequences from many distinct gene families have been reported so far, and all but two (both from plants) have been found in triploblast metazoans. The complex needs of neuronal integration and neuromuscular transmission in triploblasts require exquisite control of cellular excitability. This is in large part achieved by an extensive and diverse set of K+ channels.(ABSTRACT TRUNCATED AT 250 WORDS)
刺胞动物和纤毛原生动物是研究钾离子通道进化的具有进化意义的有趣系统发育类群。刺胞动物门是一个原始的后生动物门,由简单的双胚层生物组成,这些生物只有很少的组织类型,如水母、水螅、海葵和珊瑚。它们与后生动物其他类群的分化可能比主要三胚层门的辐射早几亿年(莫里斯,1993年)。刺胞动物是具有有组织神经系统的最原始后生动物。因此,将从刺胞动物中克隆的钾离子通道与从更高级后生动物中克隆的通道进行比较,可能会揭示哪些类型的钾离子通道对神经系统的电兴奋性最为重要。相比之下,像草履虫这样的纤毛原生动物中的通道可能并非用于在细胞间传递电信号,而仅仅是为了控制单个细胞的行为,比如逃避反应。因此,将克隆的草履虫钾离子通道与从刺胞动物和其他后生动物中克隆的钾离子通道进行比较,可能会揭示哪些类型的钾离子通道对真核生物的电兴奋性最为重要,以及哪些钾离子通道专门用于神经元信号传递。钾离子通道参与多种任务,并且普遍存在于真核生物中。钾离子通道设定了大多数后生动物和原生动物细胞的静息膜电位,并且实际上是所有真核系统中膜电活动的基本组成部分。这些通道控制后生动物动作电位的形状、持续时间和频率,并且已知也参与原生动物、真菌和植物的动作电位(希尔,1992年)。电压钳记录表明,各种不同类型的电压门控钾离子通道以及钙激活钾离子通道在真核生物中广泛存在(希尔,1992年)。因此,钾离子通道似乎对所有真核生物类群的行为反应都至关重要,包括后生动物和原生动物的运动,以及植物的快速生长反应和细胞形状变化。钾离子通道多样性在后生动物中最为显著,后生动物对电兴奋性细胞网络有很强的适应性。这些后生动物显然需要多种多样的钾离子通道亚型。到目前为止,已经报道了来自许多不同基因家族的50多个钾离子通道序列,除了两个(都来自植物)之外,所有序列都在三胚层后生动物中被发现。三胚层动物中神经元整合和神经肌肉传递的复杂需求需要对细胞兴奋性进行精确控制。这在很大程度上是通过广泛多样的钾离子通道来实现的。(摘要截断于250字)