Jessica Fratani, Gabriela Fontanarrosa, Ana Sofía Duport-Bru, Anthony Russell
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引用次数: 0
摘要
壁虎的数字特化与其攀爬能力密切相关。壁虎科(Gekkonidae)和壁虎科(Phyllodactylidae)的姊妹科中独立出现的一个经常性特征是存在新变态的副趾骨(PPEs),通常是成对的副趾骨骨骼结构,位于趾间关节和趾骨-趾骨关节附近。将 PPE 纳入革囊动物的自足茎可能会影响骨骼肢体各部分之间的信息流,从而改变祖先肢体模式的模块性和整合性。在这里,我们利用解剖网络探讨了PPE对肢体组织的影响。我们对祖先没有 PPE 的物种(鬣蜥和壁虎)和有副肢的物种(Hemidactylus mabouia 和 Uroplatus fimbriatus)的前肢和后肢进行了建模。为了进一步阐明 PPE 的影响,我们还从副瓣网络模型中删除了 PPE。我们发现,PPE 显著增加了模块化程度,在指骨上产生了紧密集成的子模块,这表明了功能特化。我们还发现了一些物种特有的奇异现象,例如在 U. fimbriatus 的肢体中,PPE 的存在有利于模块化(沿近侧轴),而趾间蹼则有利于整合(横跨侧内侧轴)。与其他骨骼元素相比,PPE的连接性较低;然而,这种连接性因其具体位置而异,似乎反映了发育限制。我们的研究结果还突显了第五跖骨在造成鳞龙类后肢极性转变方面的重要性,这与四足类更为对称的bauplan形成了鲜明对比。我们的研究结果表明,自足系统的广泛改造与新变态和引人入胜的 PPE 的增加有关。
Exploring the Influence of Neomorphic Gekkotan Paraphalanges on Limb Modularity and Integration.
Digital specializations of geckos are widely associated with their climbing abilities. A recurring feature that has independently emerged within the sister families Gekkonidae and Phyllodactylidae is the presence of neomorphic paraphalanges (PPEs), usually paired, paraxial skeletal structures lying adjacent to interphalangeal and metapodial-phalangeal joints. The incorporation of PPEs into gekkotan autopodia has the potential to modify the modularity and integration of the ancestral limb pattern by affecting information flow among skeletal limb parts. Here we explore the influence of PPEs on limb organization using anatomical networks. We modeled the fore- and hindlimbs in species ancestrally devoid of PPEs (Iguana iguana and Gekko gecko) and paraphalanx-bearing species (Hemidactylus mabouia and Uroplatus fimbriatus). To further clarify the impact of PPEs we also expunged PPEs from paraphalanx-bearing network models. We found that PPEs significantly increase modularity, giving rise to tightly integrated sub-modules along the digits, suggesting functional specialization. Species-specific singularities also emerged, such as the trade-off between the presence of PPEs favoring modularity (along the proximodistal axis) and the interdigital webbing favoring integration (across the lateromedial axis) in the limbs of U. fimbriatus. The PPEs are characterized by low connectivity compared with other skeletal elements; nevertheless, this varies based on their specific location and seemingly reflects developmental constraints. Our results also highlight the importance of the fifth metatarsal in generating a shift in lepidosaurian hindlimb polarity that contrasts with the more symmetrical bauplan of tetrapods. Our findings support extensive modification of the autopodial system in association with the addition of the neomorphic and intriguing PPEs.
期刊介绍:
Developmental Evolution is a branch of evolutionary biology that integrates evidence and concepts from developmental biology, phylogenetics, comparative morphology, evolutionary genetics and increasingly also genomics, systems biology as well as synthetic biology to gain an understanding of the structure and evolution of organisms.
The Journal of Experimental Zoology -B: Molecular and Developmental Evolution provides a forum where these fields are invited to bring together their insights to further a synthetic understanding of evolution from the molecular through the organismic level. Contributions from all these branches of science are welcome to JEZB.
We particularly encourage submissions that apply the tools of genomics, as well as systems and synthetic biology to developmental evolution. At this time the impact of these emerging fields on developmental evolution has not been explored to its fullest extent and for this reason we are eager to foster the relationship of systems and synthetic biology with devo evo.