Department for Evolutionary Biology, Max-Planck Institute for Developmental Biology, Tübingen, Germany.
Adv Exp Med Biol. 2012;751:79-91. doi: 10.1007/978-1-4614-3567-9_4.
Changes in the developmental processes and developmental mechanisms can result in the modification of morphological structures and in the evolution of phenotypic novelty. But how do developmental processes evolve? One striking finding in modern biology is the confrontation of morphological diversity in multicellular organisms with the conserved blueprint of life-the small number of conserved signaling pathways and transcriptional regulators. Evolutionary developmental biology (evo-devo) tries to explain this discrepancy between macroscopic diversity and molecular uniformity. Selected case studies in evo-devo models allowed detailed insight into the mechanisms of evolutionary changes and might help solving this problem. Here, I compare the formation of vulva development between Caenorhabditis elegans and the evo-devo model Pristionchus pacificus. More than 3 decades of work in C. elegans and 15 years in P. pacificus provide an insight into the molecular mechanisms of developmental change during vulva evolution. C. elegans and P. pacificus differ first, in the type of the signaling system used for vulva induction; second, the cells required for the inductive interactions; third, the logic of the signal system, and finally, the sequence and structure of peptide domains in otherwise conserved proteins. Nonetheless, the vulva is formed from the same three cells in both nematodes. I discuss redundancy as an evolutionary mechanism to explain developmental systems drift, a theory predicting conserved morphological structures to be generated by diverse molecular regulatory networks.
发育过程和发育机制的变化会导致形态结构的改变和表型新颖性的进化。但是,发育过程是如何进化的呢?现代生物学的一个惊人发现是,多细胞生物的形态多样性与生命的保守蓝图——少数保守的信号通路和转录调节剂——相冲突。进化发育生物学(evo-devo)试图解释这种宏观多样性和分子均匀性之间的差异。在 evo-devo 模型中的一些选定案例研究使我们能够深入了解进化变化的机制,并可能有助于解决这个问题。在这里,我比较了秀丽隐杆线虫和 evo-devo 模型太平洋扁虫的外阴发育形成。在秀丽隐杆线虫中进行了 30 多年的工作,在太平洋扁虫中进行了 15 年的工作,使我们深入了解了在外阴进化过程中发育变化的分子机制。秀丽隐杆线虫和太平洋扁虫首先在外阴诱导中使用的信号系统类型上有所不同;其次,在诱导相互作用中所需的细胞;第三,信号系统的逻辑;最后,在保守蛋白中肽结构域的序列和结构也有所不同。尽管如此,在外阴形成过程中,两种线虫都使用相同的三个细胞。我讨论了冗余作为一种进化机制,以解释发育系统的漂移,该理论预测保守的形态结构是由不同的分子调节网络产生的。