Zigler K S, Lessios H A
Smithsonian Tropical Research Institute, Balboa, Panama.
Mol Biol Evol. 2003 Feb;20(2):220-31. doi: 10.1093/molbev/msg020.
Bindin, a sea urchin sperm protein, mediates sperm-egg attachment and membrane fusion and is thus important in species recognition and speciation. Patterns of bindin variation differed among three genera that had been studied previously. In two genera of the superorder Camarodonta, Echinometra and Strongylocentrotus, both of which contain sympatric species, bindin is highly variable within and between species; a region of the molecule evolves at high rates under strong positive selection. In Arbacia, which belongs to the superorder Stirodonta and whose extant species are all allopatric, bindin variation is low, and there is no evidence of positive selection. We cloned and sequenced bindin from Tripneustes, a sea urchin that belongs to the Camarodonta but whose three species are found in different oceans. Worldwide sampling of bindin alleles shows that the bindin of Tripneustes (1) contains the highly conserved core characteristic of all other bindins characterized to date, (2) has an intron in the same position, and (3) has approximately the same length. Its structure is more like that of bindin from other camarodont sea urchins than to bindin from the stirodont ARBACIA: The resemblances to other camarodonts include a glycine-rich repeat structure upstream of the core and lack of a hydrophobic domain 3' of the core, a characteristic of Arbacia bindin. Yet the mode of evolution of Tripneustes bindin is more like that of Arbacia. Differences between bindins of the Caribbean Tripneustes ventricosus and the eastern Pacific T. depressus, separated for 3 my by the Isthmus of Panama, are limited to four amino acid changes and a single indel. There are no fixed amino acid differences or indels between T. depressus from the eastern Pacific and T. gratilla from the Indo-Pacific. Bindin of Tripneustes, like that of Arbacia, also shows no evidence of diversifying selection that would manifest itself in a higher proportion of amino acid replacements than of silent nucleotide substitutions. When the rate of intrageneric bindin divergence is standardized by dividing it by cytochrome oxidase I (COI) divergence, Tripneustes and Arbacia show a lower ratio of bindin to COI substitutions between the species of each genus than exists between the species of either Echinometra or Strongylocentrotus. Thus, mode of bindin evolution is not correlated with phylogenetic affinities or molecular structure, but rather with whether the species in a genus are allopatric or sympatric. For a molecule involved in gametic recognition, this would suggest a pattern of evolution via reinforcement. However, in bindin the process that gave rise to this pattern is not likely to have been selection to avoid hybridization, because there is no excess of amino acid replacements between species versus within species in the bindins of Echinometra and Strongylocentrotus, as would have been expected if specific recognition were the driving force in their evolution. We suggest instead that the pattern of reinforcement is a secondary effect of the ability of species with rapidly evolving bindins to coexist in sympatry.
结合蛋白是一种海胆精子蛋白,介导精卵附着和膜融合,因此在物种识别和物种形成中很重要。先前研究的三个属中,结合蛋白的变异模式有所不同。在真海胆亚纲的两个属,即艾氏海胆属和强壮海胆属中,都包含同域分布的物种,结合蛋白在种内和种间高度可变;分子的一个区域在强烈的正选择下以高速度进化。在属于旋海胆亚纲的刺海胆属中,其现存物种都是异域分布的,结合蛋白变异低,且没有正选择的证据。我们克隆并测序了来自三列海胆属的结合蛋白,三列海胆属于真海胆亚纲,但其三个物种分布在不同海洋。对结合蛋白等位基因进行全球采样表明,三列海胆的结合蛋白:(1)包含迄今已鉴定的所有其他结合蛋白的高度保守核心特征;(2)在相同位置有一个内含子;(3)长度大致相同。其结构与其他真海胆亚纲海胆的结合蛋白更相似,而与旋海胆亚纲的刺海胆属的结合蛋白不同:与其他真海胆亚纲的相似之处包括核心上游富含甘氨酸的重复结构,以及核心3'端缺乏疏水结构域,这是刺海胆属结合蛋白的一个特征。然而,三列海胆结合蛋白的进化模式更类似于刺海胆属。加勒比海的腹侧三列海胆和东太平洋的凹陷三列海胆被巴拿马地峡分隔了300万年,它们的结合蛋白之间的差异仅限于四个氨基酸变化和一个单碱基插入或缺失。东太平洋的凹陷三列海胆和印度-太平洋的绿三列海胆之间没有固定的氨基酸差异或插入或缺失。三列海胆的结合蛋白与刺海胆属的一样,也没有显示出多样化选择的证据,多样化选择会表现为氨基酸替换的比例高于沉默核苷酸替换。当通过将属内结合蛋白分歧率除以细胞色素氧化酶I(COI)分歧率来标准化时,三列海胆属和刺海胆属在每个属的物种之间显示出的结合蛋白与COI替换的比率低于艾氏海胆属或强壮海胆属的物种之间的比率。因此,结合蛋白的进化模式与系统发育亲缘关系或分子结构无关,而是与一个属中的物种是异域分布还是同域分布有关。对于一个参与配子识别的分子来说,这表明是通过强化作用的进化模式。然而,在结合蛋白中,产生这种模式的过程不太可能是为了避免杂交而进行的选择,因为在艾氏海胆属和强壮海胆属的结合蛋白中,物种间与物种内的氨基酸替换并没有过量,而如果特异性识别是其进化的驱动力,那么应该会出现这种过量。相反,我们认为强化模式是结合蛋白快速进化的物种在同域中共存能力的次要效应。