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Enhanced partner preference in a promiscuous species by manipulating the expression of a single gene.
Abstract
The molecular mechanisms underlying the evolution of complex behaviour are poorly understood. The mammalian genus Microtus provides an excellent model for investigating the evolution of social behaviour. Prairie voles (Microtus ochrogaster) exhibit a monogamous social structure in nature, whereas closely related meadow voles (Microtus pennsylvanicus) are solitary and polygamous. In male prairie voles, both vasopressin and dopamine act in the ventral forebrain to regulate selective affiliation between adult mates, known as pair bond formation, as assessed by partner preference in the laboratory. The vasopressin V1a receptor (V1aR) is expressed at higher levels in the ventral forebrain of monogamous than in promiscuous vole species, whereas dopamine receptor distribution is relatively conserved between species. Here we substantially increase partner preference formation in the socially promiscuous meadow vole by using viral vector V1aR gene transfer into the ventral forebrain. We show that a change in the expression of a single gene in the larger context of pre-existing genetic and neural circuits can profoundly alter social behaviour, providing a potential molecular mechanism for the rapid evolution of complex social behaviour.
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“While achieving relationship satisfaction is a primary goal for most individuals, only 37% of couples claim to be very happy in their marriage [24].”
From Could intranasal oxytocin be used to enhance relationships? Research imperatives, clinical policy, and ethical considerations (2013) · cites this paper as [24]
In the citing paper
“Pair-bonded prairie voles spend more time with their partner than with the stranger, whereas non-monogamous meadow voles (Microtus pennsylvanicus) spend little time interacting with their partner or stranger [138].”
From The Neurobiology of Love and Pair Bonding from Human and Animal Perspectives (2023) · cites this paper as [138]
In the citing paper
“Conversely, viral-mediated increases in VP AVPR1a expression induce partner preferences and increase affiliative behaviors in male prairie voles that are sexually naïve and, interestingly, also lead to partner preference formation in non-monogamous meadow voles [138,146].”
From The Neurobiology of Love and Pair Bonding from Human and Animal Perspectives (2023) · cites this paper as [138]
In the citing paper
“Over-expressing the gene encoding the prairie vole AVPR1A, Avpr1a, in the ventral pallidum of male meadow voles using viral vector-mediated gene transfer results in the ability of this promiscuous species to display partner preferences [23].”
From The prairie vole: An emerging model organism for understanding the social brain (2010) · cites this paper as [23]
In the citing paper
“Viral-mediated Avpr1a receptor overexpression studies show that species differences in Avpr1a expression mediate species differences in social behavior, and variation in Avpr1a expression in the brain is related to microsatellite diversity in the gene's 5′ flanking region (151-154).”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [152]
Citations
Cites
Kleiman, D. G. (1977) · The Quarterly Review of Biology · doi:10.1086/409721 · Cited by 1,436
A role for central vasopressin in pair bonding in monogamous prairie voles
Winslow, J. T., Hastings, N., Carter, C. S., Harbaugh, C. R., & Insel, T. R. (1993) · Nature · doi:10.1038/365545a0 · Cited by 948 · cited 1×
“Central administration of vasopressin facilitates each of these monogamous-typical behaviours in male prairie voles through V1aRs in the brai”
BackgroundBielsky, I. F., Hu, S.-B., Szegda, K. L., Westphal, H., & Young, L. J. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300360 · Cited by 531
Self-citationYoung, L. J., Nilsen, R., Waymire, K. G., MacGregor, G. R., & Insel, T. R. (1999) · Nature · doi:10.1038/23475 · Cited by 488
Self-citationInsel, T., Wang, Z., & Ferris, C. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-09-05381.1994 · Cited by 454
Self-citationVasopressin and oxytocin receptors in the central nervous system
Tribollet, E., & Barberis, C. (1996) · Critical Reviews™ in Neurobiology · doi:10.1615/critrevneurobiol.v10.i1.60 · Cited by 399
Role of septal vasopressin innervation in paternal behavior in prairie voles (Microtus ochrogaster).
Wang, Z., Ferris, C. F., & De Vries, G. J. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.1.400 · Cited by 381
Self-citationA critical role for nucleus accumbens dopamine in partner-preference formation in male prairie voles
Aragona, B. J., Liu, Y., Curtis, J. T., Stephan, F. K., & Wang, Z. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03483.2003 · Cited by 351
Self-citationGingrich, B., Liu, Y., Cascio, C., Wang, Z., & Insel, T. R. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.1.173 · Cited by 339
Self-citationVasopressin-dependent neural circuits underlying pair bond formation in the monogamous prairie vole
Lim, M. M., & Young, L. J. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.12.008 · Cited by 322
Self-citation
Research works printed but not linked: 1
- Aragona, B. J. et al. Opposite modulation of social attachment by D1- and D2-type dopamine receptor activation in nucleus accumbens shell. Horm. Behav. 44, 37 (2003)
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Young, L. J., & Wang, Z. (2004) · Nature Neuroscience · doi:10.1038/nn1327 · Cited by 1,523
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“pecially in males (Caldwell, Lee, Macbeth, & Young, 2008; Lim et al., 2004).”
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Metadata
- Authors
- Lim, M. M., Wang, Z., Olazábal, D. E., Ren, X., Terwilliger, E. F., & Young, L. J.
- Affiliations
- Emory University (US)
- Florida State University (US)
- Beth Israel Deaconess Medical Center (US)
- Corresponding author
- Young, Larry J.
- Venue
- Nature
- Published
- 2004-06
- Volume
- 429
- Issue
- 6993
- Pages
- 754-757
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2022927508
- Cited by
- 628
- References
- 29
- Citations by year
- 2026: 19 · 2025: 20 · 2024: 17 · 2023: 17 · 2022: 42 · 2021: 18 · 2020: 18 · 2019: 15 · 2018: 24 · 2017: 27 · 2016: 28 · 2015: 24 · 2014: 32 · 2013: 29 · 2012: 33
- FWCI
- 58.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Science Foundation
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Behavior and Reproduction
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- mate preferences, pair bonding, vasopressin V1a receptor, Microtus pennsylvanicus, Microtus ochrogaster, Microtus, evolution of social behavior, ventral forebrain, dopamine, viral gene delivery, monogamy, polygamy, promiscuity
- MeSH terms
- Animals, Choice Behavior, Arvicolinae, Female, Male, Pair Bond, Receptors, Dopamine, Sexual Behavior, Animal, Prosencephalon, Receptors, Vasopressin
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