{"title":"鸟鸣进化中的组织保护与灵活性与鸟类运动控制","authors":"Bradley M. Colquitt","doi":"10.1159/000525019","DOIUrl":null,"url":null,"abstract":"Birds and mammals have independently evolved complex behavioral and cognitive capabilities yet have markedly different brain structures. An open question is to what extent, despite these differences in anatomy, birds and mammals have evolved similar neural solutions to complex motor control and at what level of organization these similarities might lie. Courtship song in songbirds, a learned motor skill that is similar to the fine motor skills of many mammals including human speech, provides a powerful system in which to study the links connecting the development and evolution of cells, circuits, and behavior. Until recently, obtaining cellular-resolution views of the specialized neural circuitry that subserves birdsong was impossible due to a lack of molecular tools for songbirds. However, the ongoing revolution in cellular profiling and genomics offers unprecedented opportunities for molecular analysis in organisms that lack a traditional genetic infrastructure but have tractable, well-defined behaviors. Here, I describe recent efforts to understand the evolutionary relationships between birdsong control circuitry and mammalian neocortical circuitry using new approaches to measure gene expression in single cells. These results, combined with foundational work relating avian and mammalian brains at a range of biological levels, present an emerging view that amniote pallium evolution is a story of diverse neural circuit architectures employing conserved neuronal elements within a conserved topological framework. This view suggests that one locus of pallial neural circuit evolution lies at the intersection between the gene regulatory programs that regulate regional patterning and those that specify functional identity. Modifications to this intersection may underlie the evolution of pallial motor control in birds in general and to the evolutionary and developmental relationships of these circuits to the avian pallial amygdala.","PeriodicalId":56328,"journal":{"name":"Brain Behavior and Evolution","volume":"97 1","pages":"255 - 264"},"PeriodicalIF":2.1000,"publicationDate":"2022-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Organizational Conservation and Flexibility in the Evolution of Birdsong and Avian Motor Control\",\"authors\":\"Bradley M. Colquitt\",\"doi\":\"10.1159/000525019\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Birds and mammals have independently evolved complex behavioral and cognitive capabilities yet have markedly different brain structures. An open question is to what extent, despite these differences in anatomy, birds and mammals have evolved similar neural solutions to complex motor control and at what level of organization these similarities might lie. Courtship song in songbirds, a learned motor skill that is similar to the fine motor skills of many mammals including human speech, provides a powerful system in which to study the links connecting the development and evolution of cells, circuits, and behavior. Until recently, obtaining cellular-resolution views of the specialized neural circuitry that subserves birdsong was impossible due to a lack of molecular tools for songbirds. However, the ongoing revolution in cellular profiling and genomics offers unprecedented opportunities for molecular analysis in organisms that lack a traditional genetic infrastructure but have tractable, well-defined behaviors. Here, I describe recent efforts to understand the evolutionary relationships between birdsong control circuitry and mammalian neocortical circuitry using new approaches to measure gene expression in single cells. These results, combined with foundational work relating avian and mammalian brains at a range of biological levels, present an emerging view that amniote pallium evolution is a story of diverse neural circuit architectures employing conserved neuronal elements within a conserved topological framework. This view suggests that one locus of pallial neural circuit evolution lies at the intersection between the gene regulatory programs that regulate regional patterning and those that specify functional identity. Modifications to this intersection may underlie the evolution of pallial motor control in birds in general and to the evolutionary and developmental relationships of these circuits to the avian pallial amygdala.\",\"PeriodicalId\":56328,\"journal\":{\"name\":\"Brain Behavior and Evolution\",\"volume\":\"97 1\",\"pages\":\"255 - 264\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2022-05-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain Behavior and Evolution\",\"FirstCategoryId\":\"102\",\"ListUrlMain\":\"https://doi.org/10.1159/000525019\",\"RegionNum\":4,\"RegionCategory\":\"心理学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BEHAVIORAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Behavior and Evolution","FirstCategoryId":"102","ListUrlMain":"https://doi.org/10.1159/000525019","RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
Organizational Conservation and Flexibility in the Evolution of Birdsong and Avian Motor Control
Birds and mammals have independently evolved complex behavioral and cognitive capabilities yet have markedly different brain structures. An open question is to what extent, despite these differences in anatomy, birds and mammals have evolved similar neural solutions to complex motor control and at what level of organization these similarities might lie. Courtship song in songbirds, a learned motor skill that is similar to the fine motor skills of many mammals including human speech, provides a powerful system in which to study the links connecting the development and evolution of cells, circuits, and behavior. Until recently, obtaining cellular-resolution views of the specialized neural circuitry that subserves birdsong was impossible due to a lack of molecular tools for songbirds. However, the ongoing revolution in cellular profiling and genomics offers unprecedented opportunities for molecular analysis in organisms that lack a traditional genetic infrastructure but have tractable, well-defined behaviors. Here, I describe recent efforts to understand the evolutionary relationships between birdsong control circuitry and mammalian neocortical circuitry using new approaches to measure gene expression in single cells. These results, combined with foundational work relating avian and mammalian brains at a range of biological levels, present an emerging view that amniote pallium evolution is a story of diverse neural circuit architectures employing conserved neuronal elements within a conserved topological framework. This view suggests that one locus of pallial neural circuit evolution lies at the intersection between the gene regulatory programs that regulate regional patterning and those that specify functional identity. Modifications to this intersection may underlie the evolution of pallial motor control in birds in general and to the evolutionary and developmental relationships of these circuits to the avian pallial amygdala.
期刊介绍:
''Brain, Behavior and Evolution'' is a journal with a loyal following, high standards, and a unique profile as the main outlet for the continuing scientific discourse on nervous system evolution. The journal publishes comparative neurobiological studies that focus on nervous system structure, function, or development in vertebrates as well as invertebrates. Approaches range from the molecular over the anatomical and physiological to the behavioral. Despite this diversity, most papers published in ''Brain, Behavior and Evolution'' include an evolutionary angle, at least in the discussion, and focus on neural mechanisms or phenomena. Some purely behavioral research may be within the journal’s scope, but the suitability of such manuscripts will be assessed on a case-by-case basis. The journal also publishes review articles that provide critical overviews of current topics in evolutionary neurobiology.