{"title":"GABA 能中间神经元状态调节的转录组相关性:跨物种分析","authors":"Joram Keijser, Loreen Hertäg, Henning Sprekeler","doi":"10.1523/JNEUROSCI.2371-23.2024","DOIUrl":null,"url":null,"abstract":"<p><p>GABAergic inhibitory interneurons comprise many subtypes that differ in their molecular, anatomical, and functional properties. In mouse visual cortex, they also differ in their modulation with an animal's behavioral state, and this state modulation can be predicted from the first principal component (PC) of the gene expression matrix. Here, we ask whether this link between transcriptome and state-dependent processing generalizes across species. To this end, we analysed seven single-cell and single-nucleus RNA sequencing datasets from mouse, human, songbird, and turtle forebrains. Despite homology at the level of cell types, we found clear differences between transcriptomic PCs, with greater dissimilarities between evolutionarily distant species. These dissimilarities arise from two factors: divergence in gene expression within homologous cell types and divergence in cell-type abundance. We also compare the expression of cholinergic receptors, which are thought to causally link transcriptome and state modulation. Several cholinergic receptors predictive of state modulation in mouse interneurons are differentially expressed between species. Circuit modelling and mathematical analyses suggest conditions under which these expression differences could translate into functional differences.</p>","PeriodicalId":50114,"journal":{"name":"Journal of Neuroscience","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11529809/pdf/","citationCount":"0","resultStr":"{\"title\":\"Transcriptomic Correlates of State Modulation in GABAergic Interneurons: A Cross-Species Analysis.\",\"authors\":\"Joram Keijser, Loreen Hertäg, Henning Sprekeler\",\"doi\":\"10.1523/JNEUROSCI.2371-23.2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>GABAergic inhibitory interneurons comprise many subtypes that differ in their molecular, anatomical, and functional properties. In mouse visual cortex, they also differ in their modulation with an animal's behavioral state, and this state modulation can be predicted from the first principal component (PC) of the gene expression matrix. Here, we ask whether this link between transcriptome and state-dependent processing generalizes across species. To this end, we analysed seven single-cell and single-nucleus RNA sequencing datasets from mouse, human, songbird, and turtle forebrains. Despite homology at the level of cell types, we found clear differences between transcriptomic PCs, with greater dissimilarities between evolutionarily distant species. These dissimilarities arise from two factors: divergence in gene expression within homologous cell types and divergence in cell-type abundance. We also compare the expression of cholinergic receptors, which are thought to causally link transcriptome and state modulation. Several cholinergic receptors predictive of state modulation in mouse interneurons are differentially expressed between species. Circuit modelling and mathematical analyses suggest conditions under which these expression differences could translate into functional differences.</p>\",\"PeriodicalId\":50114,\"journal\":{\"name\":\"Journal of Neuroscience\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-10-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11529809/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1523/JNEUROSCI.2371-23.2024\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1523/JNEUROSCI.2371-23.2024","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
GABA 能抑制性中间神经元包括许多亚型,它们的分子、解剖和功能特性各不相同。在小鼠的视觉皮层中,它们也因动物的行为状态而异,这种状态调节可以通过基因表达矩阵的第一个主成分(PC)来预测。在此,我们想知道转录组与状态依赖性处理之间的这种联系是否会在不同物种之间普遍存在。为此,我们分析了来自小鼠、人类、鸣禽和海龟前脑的七个单细胞和单核 RNA 测序数据集。尽管在细胞类型水平上存在同源性,但我们发现转录组 PC 之间存在明显差异,进化距离较远的物种之间差异更大。这些差异来自两个因素:同源细胞类型内基因表达的差异和细胞类型丰度的差异。我们还对胆碱能受体的表达进行了比较,胆碱能受体被认为与转录组和状态调节有因果关系。在小鼠中间神经元中,几种可预测状态调节的胆碱能受体在不同物种间的表达存在差异。电路建模和数学分析表明了这些表达差异转化为功能差异的条件。抑制性中间神经元是一个特别多样化的细胞群,因其抑制作用而得名。这些中间神经元会根据动物的行为状态改变其活性--至少在小鼠中是如此。在这里,我们通过比较人类、海龟和斑马雀中间神经元的基因表达模式,研究这一发现是否适用于其他物种。尽管有着共同的进化历史,但我们发现只有人类和小鼠的中间神经元具有与状态调节相关的相似基因表达模式。一个数学模型表明,单个细胞的表达差异会转化为网络层面的功能差异。
Transcriptomic Correlates of State Modulation in GABAergic Interneurons: A Cross-Species Analysis.
GABAergic inhibitory interneurons comprise many subtypes that differ in their molecular, anatomical, and functional properties. In mouse visual cortex, they also differ in their modulation with an animal's behavioral state, and this state modulation can be predicted from the first principal component (PC) of the gene expression matrix. Here, we ask whether this link between transcriptome and state-dependent processing generalizes across species. To this end, we analysed seven single-cell and single-nucleus RNA sequencing datasets from mouse, human, songbird, and turtle forebrains. Despite homology at the level of cell types, we found clear differences between transcriptomic PCs, with greater dissimilarities between evolutionarily distant species. These dissimilarities arise from two factors: divergence in gene expression within homologous cell types and divergence in cell-type abundance. We also compare the expression of cholinergic receptors, which are thought to causally link transcriptome and state modulation. Several cholinergic receptors predictive of state modulation in mouse interneurons are differentially expressed between species. Circuit modelling and mathematical analyses suggest conditions under which these expression differences could translate into functional differences.
期刊介绍:
JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles