Molecular evolution of K+ channels in primitive eukaryotes.

T Jegla, L Salkoff
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引用次数: 0

Abstract

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)

原始真核生物中K+通道的分子演化。
刺胞动物和纤毛虫原生动物是研究K+通道进化的重要进化类群。刺胞动物是一种原始的后生动物门,由简单的双胚层生物组成,其组织类型很少,如水母、水螅、海葵和珊瑚。它们与其他后生动物的分化可能比主要的三虫门的辐射早几亿年(Morris, 1993)。刺胞动物是具有有组织的神经系统的最原始的后生动物。因此,比较从刺胞动物克隆的K+通道和从更高级的后生动物克隆的K+通道可能揭示哪种类型的K+通道对神经系统的电兴奋性最基本。相比之下,草履虫等纤毛虫原生动物的通道可能不是为了在细胞之间传递电信号而设计的,而只是为了控制单个细胞的行为,比如回避反应。因此,将克隆的草履虫K+通道与从刺胞动物和其他后生动物克隆的K+通道进行比较,可能会揭示真核生物中哪种类型的K+通道对电兴奋性最基本,以及哪种K+通道专门用于神经元信号传导。钾通道参与多种任务,普遍存在于真核生物中。K+通道设置大多数后生动物和原生动物细胞的静息膜电位,是几乎所有真核生物系统中膜电活动的基本组成部分。这些通道控制着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(Hille, 1992)。电压钳记录显示,各种各样的电压门控K+通道以及Ca(2+)激活的K+通道在真核生物中广泛存在(Hille, 1992)。因此,K+通道似乎对所有真核生物的行为反应至关重要,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。到目前为止,K+通道的多样性在后生动物中是最大的,它们对电兴奋的细胞网络做出了强有力的承诺。这些后生动物显然需要多种多样的K+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K+通道序列,除了两个(都来自植物)之外,其余都是在三倍体后生动物中发现的。三倍体细胞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细的控制。这在很大程度上是通过广泛和多样化的K+渠道实现的。(摘要删节250字)
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