在动物气质模型中,海马体中与生物能量相关的基因表达预测内化与外化行为。

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Frontiers in Molecular Neuroscience Pub Date : 2025-03-04 eCollection Date: 2025-01-01 DOI:10.3389/fnmol.2025.1469467
Elaine K Hebda-Bauer, Megan H Hagenauer, Daniel B Munro, Peter Blandino, Fan Meng, Keiko Arakawa, John D H Stead, Apurva S Chitre, A Bilge Ozel, Pejman Mohammadi, Stanley J Watson, Shelly B Flagel, Jun Li, Abraham A Palmer, Huda Akil
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引用次数: 0

摘要

外化和内化行为倾向是许多精神疾病和物质使用障碍的基础。这些倾向与气质上的差异有关,这种差异在发育早期通过遗传和环境因素的相互作用而出现。为了更好地理解气质的神经生物学,我们选择性地培育了两代行为高度不同的大鼠:繁殖的低反应(bLRs)在新环境中高度抑制和焦虑,而繁殖的高反应(bHRs)则高度探索,寻求感觉,并倾向于寻求药物行为。最近,我们通过交叉bhr和blr (F0-F1-F2)来描述这些遗传差异,以产生具有良好特征的谱系和行为(探索性运动,焦虑样行为,巴甫洛夫条件反射)的异质F2样本。已确定的遗传位点包含可以通过多种机制影响行为的变异,包括对基因表达的近端影响。在这里,我们使用海马RNA-Seq测量了雄性和雌性F0s (n = 12个bHRs, 12个bLRs)和异质F2s (n = 250)的大样本中的基因表达。这使得行为与遗传和功能基因组数据的三角测量能够暗示特定的基因和生物学途径。我们的研究结果表明,bHR/bLR差异基因的表达是稳健的,在表达上超越了性别差异,并预测了与F2行为相关的表达。在F0和F2样本中,与生长/增殖相关的基因集随着bhr样行为而上调,而与线粒体功能、氧化应激和小胶质细胞激活相关的基因集则随着blr样行为而上调。将我们的F2 RNA-Seq数据与之前收集的全基因组测序数据整合,确定了海马表达与近端遗传变异相关的基因(顺式表达数量性状位点或顺式- eqtl)。这些顺式eqtl成功预测了基于F0基因型的bHR/bLR差异基因表达。这些基因中有16个与cis- eqtl相关,这些基因位于我们之前与行为相关的位点内,是介导遗传变异对行为气质影响的有力候选者。其中8个基因与生物能量学有关。我们的研究与其他针对类似行为特征的研究的趋同表明,还有五个基因与气质始终相关。总的来说,我们的研究结果暗示了海马生物能量调节氧化应激、小胶质细胞激活和生长相关过程在塑造行为气质中,从而调节对精神和成瘾障碍的脆弱性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioenergetic-related gene expression in the hippocampus predicts internalizing vs. externalizing behavior in an animal model of temperament.

Externalizing and internalizing behavioral tendencies underlie many psychiatric and substance use disorders. These tendencies are associated with differences in temperament that emerge early in development via the interplay of genetic and environmental factors. To better understand the neurobiology of temperament, we have selectively bred rats for generations to produce two lines with highly divergent behavior: bred Low Responders (bLRs) are highly inhibited and anxious in novel environments, whereas bred High Responders (bHRs) are highly exploratory, sensation-seeking, and prone to drug-seeking behavior. Recently, we delineated these heritable differences by intercrossing bHRs and bLRs (F0-F1-F2) to produce a heterogeneous F2 sample with well-characterized lineage and behavior (exploratory locomotion, anxiety-like behavior, Pavlovian conditioning). The identified genetic loci encompassed variants that could influence behavior via many mechanisms, including proximal effects on gene expression. Here we measured gene expression in male and female F0s (n = 12 bHRs, 12 bLRs) and in a large sample of heterogeneous F2s (n = 250) using hippocampal RNA-Seq. This enabled triangulation of behavior with both genetic and functional genomic data to implicate specific genes and biological pathways. Our results show that bHR/bLR differential gene expression is robust, surpassing sex differences in expression, and predicts expression associated with F2 behavior. In F0 and F2 samples, gene sets related to growth/proliferation are upregulated with bHR-like behavior, whereas gene sets related to mitochondrial function, oxidative stress, and microglial activation are upregulated with bLR-like behavior. Integrating our F2 RNA-Seq data with previously-collected whole genome sequencing data identified genes with hippocampal expression correlated with proximal genetic variation (cis-expression quantitative trait loci or cis-eQTLs). These cis-eQTLs successfully predict bHR/bLR differential gene expression based on F0 genotype. Sixteen of these genes are associated with cis-eQTLs colocalized within loci we previously linked to behavior and are strong candidates for mediating the influence of genetic variation on behavioral temperament. Eight of these genes are related to bioenergetics. Convergence between our study and others targeting similar behavioral traits revealed five more genes consistently related to temperament. Overall, our results implicate hippocampal bioenergetic regulation of oxidative stress, microglial activation, and growth-related processes in shaping behavioral temperament, thereby modulating vulnerability to psychiatric and addictive disorders.

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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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