Tunicate tails, stolons, and the origin of the vertebrate trunk.

T C Lacalli
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Abstract

Tunicates are primitive chordates that develop a transient 'tail' in the larval stage that is generally interpreted as a rudimentary version of the vertebrate trunk. Not all tunicates have tails, however. The groups that lack them, salps and pyrosomes, instead have a trunk-like reproductive stolon located approximately where the tail would otherwise be. In salps, files of blastozooids are formed along the sides of the stolon. The tail and caudal trunk in more advanced chordates could have evolved from a stolon of this type, an idea referred to here as the 'stolon hypothesis'. This means the vertebrate body could be a composite structure, since there is the potential for each somite to incorporate elements originally derived from a complete functional zooid. If indeed this has occurred, it should be reflected in some fashion in gene expression patterns in the vertebrate trunk. Selected morphological and molecular data are reviewed to show that they provide some circumstantial support for the stolon hypothesis. The case would be stronger if it could be demonstrated that salps and/or pyrosomes are ancestral to other tunicates. The molecular phylogenies so far available generally support the idea of a pelagic ancestor, but offer only limited guidance as to which of the surviving pelagic groups most closely resembles it. The principal testable prediction of the stolon hypothesis is that head structures (or their homologues) should be duplicated in series in the trunk in advanced chordates, and vice versa, i.e. trunk structures should occur in the head. The distribution of both rhabdomeric photoreceptors and nephridia in amphioxus conform with this prediction. Equally striking is the involvement of the Pax2 gene in the development of both the inner ear and nephric ducts in vertebrates. The stolon hypothesis would explain this as a consequence of the common origin of otic capsules and excretory ducts from atrial rudiments: from the paired rudiments of the parent oozooid in the case of the otic capsule (these express Pax2 according to recent ascidian data), and from tubular rudiments in the stolon in the case of the excretory ducts.

被束状的尾巴、匍匐茎和脊椎动物躯干的起源。
被囊动物是原始脊索动物,在幼虫阶段发育出短暂的“尾巴”,通常被解释为脊椎动物躯干的初级版本。然而,并不是所有的被囊动物都有尾巴。没有它们的类群,如海鞘和火小体,取而代之的是位于尾巴位置的树干状生殖匍匐茎。在海鞘中,沿着匍匐茎的两侧形成了胚形体。更高级脊索动物的尾巴和尾端躯干可能是从这种类型的匍匐茎进化而来的,这个想法在这里被称为“匍匐茎假说”。这意味着脊椎动物的身体可能是一个复合结构,因为每个小体都有可能包含最初来自完整功能动物的元素。如果这确实发生了,它应该以某种方式反映在脊椎动物躯干的基因表达模式中。选择形态学和分子数据进行审查,以表明他们提供一些间接支持匍匐茎假说。如果能证明海鞘和/或火体是其他被囊动物的祖先,这种情况就会更有力。到目前为止,现有的分子系统发育学总体上支持上层生物祖先的观点,但对于现存的上层生物群体中哪一个与上层生物最相似,只能提供有限的指导。匍匐茎假说的主要可测试的预测是,头部结构(或其同源物)应该在高级脊索动物的躯干中连续复制,反之亦然,即躯干结构应该出现在头部。文昌鱼横纹肌光感受器和肾结石的分布符合这一预测。同样引人注目的是Pax2基因参与了脊椎动物内耳和肾管的发育。匍匐茎假说可以解释这一现象,因为耳囊和排泄管的共同起源来自心房萌芽:在耳囊的情况下,来自亲本卵母动物的成对萌芽(根据最近的海鞘资料,这些萌芽表达Pax2),在排泄管的情况下,来自匍匐茎的管状萌芽。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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