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一个低表达的血管加压素等位基因可预防焦虑相关行为。

A hypomorphic vasopressin allele prevents anxiety-related behavior.

作者信息

Bunck Mirjam, Czibere Ludwig, Horvath Charlotte, Graf Cornelia, Frank Elisabeth, Kessler Melanie S, Murgatroyd Chris, Müller-Myhsok Bertram, Gonik Mariya, Weber Peter, Pütz Benno, Muigg Patrik, Panhuysen Markus, Singewald Nicolas, Bettecken Thomas, Deussing Jan M, Holsboer Florian, Spengler Dietmar, Landgraf Rainer

机构信息

Max Planck Institute of Psychiatry, Munich, Germany.

出版信息

PLoS One. 2009;4(4):e5129. doi: 10.1371/journal.pone.0005129. Epub 2009 Apr 9.

Abstract

BACKGROUND

To investigate neurobiological correlates of trait anxiety, CD1 mice were selectively bred for extremes in anxiety-related behavior, with high (HAB) and low (LAB) anxiety-related behavior mice additionally differing in behavioral tests reflecting depression-like behavior.

METHODOLOGY/ PRINCIPAL FINDINGS: In this study, microarray analysis, in situ hybridization, quantitative real-time PCR and immunohistochemistry revealed decreased expression of the vasopressin gene (Avp) in the hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei of adult LAB mice compared to HAB, NAB (normal anxiety-related behavior) and HABxLAB F1 intercross controls, without detecting differences in receptor expression or density. By sequencing the regions 2.5 kbp up- and downstream of the Avp gene locus, we could identify several polymorphic loci, differing between the HAB and LAB lines. In the gene promoter, a deletion of twelve bp Delta(-2180-2191) is particularly likely to contribute to the reduced Avp expression detected in LAB animals under basal conditions. Indeed, allele-specific transcription analysis of F1 animals revealed a hypomorphic LAB-specific Avp allele with a reduced transcription rate by 75% compared to the HAB-specific allele, thus explaining line-specific Avp expression profiles and phenotypic features. Accordingly, intra-PVN Avp mRNA levels were found to correlate with anxiety-related and depression-like behaviors. In addition to this correlative evidence, a significant, though moderate, genotype/phenotype association was demonstrated in 258 male mice of a freely-segregating F2 panel, suggesting a causal contribution of the Avp promoter deletion to anxiety-related behavior.

DISCUSSION

Thus, the identification of polymorphisms in the Avp gene promoter explains gene expression differences in association with the observed phenotype, thus further strengthening the concept of the critical involvement of centrally released AVP in trait anxiety.

摘要

背景

为了研究特质焦虑的神经生物学相关性,对CD1小鼠进行选择性培育,使其在焦虑相关行为上表现出极端差异,高焦虑相关行为(HAB)小鼠和低焦虑相关行为(LAB)小鼠在反映抑郁样行为的行为测试中也存在差异。

方法/主要发现:在本研究中,微阵列分析、原位杂交、定量实时PCR和免疫组化显示,与HAB、NAB(正常焦虑相关行为)和HABxLAB F1杂交对照组相比,成年LAB小鼠下丘脑室旁核(PVN)和视上核(SON)中血管加压素基因(Avp)的表达降低,而未检测到受体表达或密度的差异。通过对Avp基因座上下游2.5kbp区域进行测序,我们鉴定出了几个多态性位点,HAB和LAB品系之间存在差异。在基因启动子中,一个12bp的缺失Delta(-2180 - 2191)特别可能导致在基础条件下LAB动物中检测到的Avp表达降低。事实上,对F1动物的等位基因特异性转录分析显示,与HAB特异性等位基因相比,LAB特异性Avp等位基因的转录率降低了75%,从而解释了品系特异性的Avp表达谱和表型特征。因此,发现PVN内Avp mRNA水平与焦虑相关和抑郁样行为相关。除了这种相关性证据外,在一个自由分离的F2群体的258只雄性小鼠中还证明了显著但适度的基因型/表型关联,表明Avp启动子缺失对焦虑相关行为有因果作用。

讨论

因此,Avp基因启动子多态性的鉴定解释了与观察到的表型相关的基因表达差异,从而进一步强化了中枢释放的AVP在特质焦虑中起关键作用的概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c2/2663030/8bbc172e3402/pone.0005129.g001.jpg

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