posted on 2024-11-14, 16:14authored byMirjam Bunck, Ludwig Czibere, Charlotte Horvath, Cornelia Graf, Elisabeth Frank, Melanie S Kebler, Chris Murgatroyd, Bertram Muller-Myhsok, Mariya Gonik, Peter Weber, Benno Putz, Patrik Muigg, Markus Panhuysen, Nicolas Singewald, Thomas Bettecken, Jan M Deussing, Florian Holsboer, Dietmar Spengler, Rainer Landgraf
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 Δ(−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.
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Citation
Bunck, M., Czibere, L., Horvath, C., Graf, C., Frank, E. T., Kebler, M. S., Murgatroyd, C., Muller-Myhsok, B., Gonik, M., Weber, P., Putz, B., Muigg, P., Panhuysen, M., Singewald, N., Bettecken, T., Deussing, J. M.., Holsboer, F., Spengler, D. & Landgraf, R. (2009). A hypomorphic vasopressin allele prevents anxiety-related behavior. PLoS One, 4 (4), 1-21.