鸟鸣进化中的组织保护与灵活性与鸟类运动控制

IF 2.1 4区 心理学 Q3 BEHAVIORAL SCIENCES Brain Behavior and Evolution Pub Date : 2022-05-27 DOI:10.1159/000525019
Bradley M. Colquitt
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引用次数: 3

摘要

鸟类和哺乳动物独立进化出复杂的行为和认知能力,但大脑结构明显不同。一个悬而未决的问题是,尽管在解剖学上存在这些差异,但鸟类和哺乳动物在多大程度上进化出了类似的神经解决方案来控制复杂的运动,以及这些相似之处可能在多大的组织水平上。鸣禽的求爱歌是一种习得的运动技能,与包括人类语言在内的许多哺乳动物的精细运动技能相似,它提供了一个强大的系统来研究连接细胞、电路和行为的发育和进化的联系。直到最近,由于缺乏用于鸣禽的分子工具,还不可能获得辅助鸟鸣的专门神经回路的细胞分辨率视图。然而,正在进行的细胞图谱和基因组学革命为缺乏传统遗传基础设施但具有易于处理、明确行为的生物体的分子分析提供了前所未有的机会。在这里,我描述了最近的努力,以了解鸟鸣控制电路和哺乳动物新皮质电路之间的进化关系,使用新的方法来测量单细胞中的基因表达。这些结果,再加上在一系列生物学水平上与鸟类和哺乳动物大脑相关的基础工作,提出了一种新的观点,即羊膜腔的进化是一个在保守拓扑框架内使用保守神经元元件的不同神经回路结构的故事。这一观点表明,大脑皮层神经回路进化的一个位点位于调节区域模式的基因调控程序和指定功能同一性的基因调控计划之间的交叉点。这种交叉点的改变可能是鸟类大脑皮层运动控制进化的基础,也是这些回路与鸟类大脑皮层杏仁核进化和发育关系的基础。
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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.
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来源期刊
Brain Behavior and Evolution
Brain Behavior and Evolution 医学-行为科学
CiteScore
3.10
自引率
23.50%
发文量
31
审稿时长
>12 weeks
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.
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