Graduate School of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8572 Japan.
Laboratory for Evolutionary Morphology, RIKEN, Kobe, 650-0047 Japan ; Department of Cytology and Histology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Okayama, 700-8558 Japan ; Sumitomo Besshi Hospital, 3-1 Oji-cho, Niihama, Ehime 792-8543 Japan.
Zoological Lett. 2016 Apr 14;2:10. doi: 10.1186/s40851-016-0046-3. eCollection 2016.
The ancestral configuration of the vertebrate head has long been an intriguing topic in comparative morphology and evolutionary biology. One peculiar component of the vertebrate head is the presence of extra-ocular muscles (EOMs), the developmental mechanism and evolution of which remain to be determined. The head mesoderm of elasmobranchs undergoes local epithelialization into three head cavities, precursors of the EOMs. In contrast, in avians, these muscles appear to develop mainly from the mesenchymal head mesoderm. Importantly, in the basal vertebrate lamprey, the head mesoderm does not show overt head cavities or signs of segmental boundaries, and the development of the EOMs is not well described. Furthermore, the disposition of the lamprey EOMs differs from those the rest of vertebrates, in which the morphological pattern of EOMs is strongly conserved. To better understand the evolution and developmental origins of the vertebrate EOMs, we explored the development of the head mesoderm and EOMs of the lamprey in detail. We found that the disposition of lamprey EOM primordia differed from that in gnathostomes, even during the earliest period of development. We also found that three components of the paraxial head mesoderm could be distinguished genetically (premandibular mesoderm: Gsc+/TbxA-; mandibular mesoderm: Gsc-/TbxA-; hyoid mesoderm: Gsc-/TbxA+), indicating that the genetic mechanisms of EOMs are conserved in all vertebrates. We conclude that the tripartite developmental origin of the EOMs is likely to have been possessed by the latest common ancestor of the vertebrates. This ancestor's EOM developmental pattern was also suggested to have resembled more that of the lamprey, and the gnathostome EOMs' disposition is likely to have been established by a secondary modification that took place in the common ancestor of crown gnathostomes.
脊椎动物头部的祖征一直是比较形态学和进化生物学中一个有趣的话题。脊椎动物头部的一个特殊组成部分是眼外肌 (EOM),其发育机制和进化仍有待确定。软骨鱼类的头部中胚层经历局部上皮化,形成三个头部腔,是 EOM 的前体。相比之下,在鸟类中,这些肌肉似乎主要由间质头部中胚层发育而来。重要的是,在基础脊椎动物七鳃鳗中,头部中胚层没有明显的头部腔或节段边界的迹象,EOM 的发育也没有很好地描述。此外,七鳃鳗 EOM 的排列方式与其他脊椎动物不同,后者的 EOM 形态模式具有很强的保守性。为了更好地理解脊椎动物 EOM 的进化和发育起源,我们详细研究了七鳃鳗头部中胚层和 EOM 的发育。我们发现,七鳃鳗 EOM 原基的排列方式与颌脊椎动物不同,甚至在发育的最早阶段也是如此。我们还发现,三个轴旁头部中胚层的成分可以在遗传上区分开来(前颌中胚层:Gsc+/TbxA-;下颌中胚层:Gsc-/TbxA-;舌骨中胚层:Gsc-/TbxA+),这表明 EOM 的遗传机制在所有脊椎动物中都是保守的。我们得出结论,EOM 的三分体发育起源很可能是在脊椎动物的最近共同祖先中拥有的。这个祖先的 EOM 发育模式也被认为更类似于七鳃鳗,而颌脊椎动物的 EOM 排列很可能是在冠颌脊椎动物的共同祖先中发生的二次修饰而建立的。