{"title":"Is there a loophole in Dollo's law? A DevoEvo perspective on irreversibility (of felid dentition)","authors":"Vincent J. Lynch","doi":"10.1002/jez.b.23163","DOIUrl":null,"url":null,"abstract":"<p>There is a longstanding interest in whether the loss of complex characters is reversible (so-called “Dollo's law”). Reevolution has been suggested for numerous traits but among the first was Kurtén, who proposed that the presence of the second lower molar (M<sub>2</sub>) of the <i>Eurasian lynx</i> (<i>Lynx lynx</i>) was a violation of Dollo's law because all other Felids lack M<sub>2</sub>. While an early and often cited example for the reevolution of a complex trait, Kurtén and Werdelin used an <i>ad hoc</i> parsimony argument to support their. Here I revisit the evidence that M<sub>2</sub> reevolved lynx using explicit parsimony and maximum likelihood models of character evolution and find strong evidence that Kurtén and Werdelin were correct—M<sub>2</sub> reevolved in <i>E. lynx</i>. Next, I explore the developmental mechanisms which may explain this violation of Dollo's law and suggest that the reevolution of lost complex traits may arise from the reevolution of cis-regulatory elements and protein−protein interactions, which have a longer half-life after silencing that protein coding genes. Finally, I present a developmental model to explain the reevolution M<sub>2</sub> in <i>E. lynx</i>, which suggest that the developmental programs required for the establishment of serially homologous characters may never really be lost so long as a single instance of the character remains—thus the gain and loss and regain of serially homologous characters, such mammalian molars, may be developmentally and evolutionarily “simple.”</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"340 8","pages":"509-517"},"PeriodicalIF":1.8000,"publicationDate":"2022-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23163","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of experimental zoology. Part B, Molecular and developmental evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jez.b.23163","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 1
Abstract
There is a longstanding interest in whether the loss of complex characters is reversible (so-called “Dollo's law”). Reevolution has been suggested for numerous traits but among the first was Kurtén, who proposed that the presence of the second lower molar (M2) of the Eurasian lynx (Lynx lynx) was a violation of Dollo's law because all other Felids lack M2. While an early and often cited example for the reevolution of a complex trait, Kurtén and Werdelin used an ad hoc parsimony argument to support their. Here I revisit the evidence that M2 reevolved lynx using explicit parsimony and maximum likelihood models of character evolution and find strong evidence that Kurtén and Werdelin were correct—M2 reevolved in E. lynx. Next, I explore the developmental mechanisms which may explain this violation of Dollo's law and suggest that the reevolution of lost complex traits may arise from the reevolution of cis-regulatory elements and protein−protein interactions, which have a longer half-life after silencing that protein coding genes. Finally, I present a developmental model to explain the reevolution M2 in E. lynx, which suggest that the developmental programs required for the establishment of serially homologous characters may never really be lost so long as a single instance of the character remains—thus the gain and loss and regain of serially homologous characters, such mammalian molars, may be developmentally and evolutionarily “simple.”
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.