The pheromone darcin drives a circuit for innate and reinforced behaviours.


Journal

Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462

Informations de publication

Date de publication:
02 2020
Historique:
received: 16 07 2018
accepted: 12 12 2019
pubmed: 31 1 2020
medline: 22 4 2020
entrez: 31 1 2020
Statut: ppublish

Résumé

Organisms have evolved diverse behavioural strategies that enhance the likelihood of encountering and assessing mates

Identifiants

pubmed: 31996852
doi: 10.1038/s41586-020-1967-8
pii: 10.1038/s41586-020-1967-8
doi:

Substances chimiques

Intercellular Signaling Peptides and Proteins 0
Mup20 protein, mouse 0
Pheromones 0
Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

137-141

Subventions

Organisme : Howard Hughes Medical Institute
Pays : United States

Références

Malte, A. Sexual Selection (Princeton Univ. Press, 1994).
Wyatt, D. T. Pheromones and Animal Behavior: Chemical Signals and Signatures (Cambridge Univ. Press, 2014).
Roberts, S. A. et al. Darcin: a male pheromone that stimulates female memory and sexual attraction to an individual male’s odour. BMC Biol. 8, 75 (2010).
doi: 10.1186/1741-7007-8-75
Roberts, S. A., Davidson, A. J., McLean, L., Beynon, R. J. & Hurst, J. L. Pheromonal induction of spatial learning in mice. Science 338, 1462–1465 (2012).
doi: 10.1126/science.1225638
Roberts, S. A., Davidson, A. J., Beynon, R. J. & Hurst, J. L. Female attraction to male scent and associative learning: The house mouse as a mammalian model. Anim. Behav. 97, 313–321 (2014).
doi: 10.1016/j.anbehav.2014.08.010
Kaur, A. W. et al. Murine pheromone proteins constitute a context-dependent combinatorial code governing multiple social behaviors. Cell 157, 676–688 (2014).
doi: 10.1016/j.cell.2014.02.025
Schultz, W. Neuronal reward and decision signals: from theories to data. Physiol. Rev. 95, 853–951 (2015).
doi: 10.1152/physrev.00023.2014
Halpern, M. & Martínez-Marcos, A. Structure and function of the vomeronasal system: an update. Prog. Neurobiol. 70, 245–318 (2003).
doi: 10.1016/S0301-0082(03)00103-5
Dulac, C. & Wagner, S. Genetic analysis of brain circuits underlying pheromone signaling. Annu. Rev. Genet. 40, 449–467 (2006).
doi: 10.1146/annurev.genet.39.073003.093937
Gradinaru, V., Thompson, K. R. & Deisseroth, K. eNpHR: a Natronomonas halorhodopsin enhanced for optogenetic applications. Brain Cell Biol. 36, 129–139 (2008).
doi: 10.1007/s11068-008-9027-6
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G. & Deisseroth, K. Millisecond-timescale, genetically targeted optical control of neural activity. Nat. Neurosci. 8, 1263–1268 (2005).
doi: 10.1038/nn1525
Root, C. M., Denny, C. A., Hen, R. & Axel, R. The participation of cortical amygdala in innate, odour-driven behaviour. Nature 515, 269–273 (2014).
doi: 10.1038/nature13897
Martín-Sánchez, A. et al. From sexual attraction to maternal aggression: when pheromones change their behavioural significance. Horm. Behav. 68, 65–76 (2015).
doi: 10.1016/j.yhbeh.2014.08.007
Kimoto, H., Haga, S., Sato, K. & Touhara, K. Sex-specific peptides from exocrine glands stimulate mouse vomeronasal sensory neurons. Nature 437, 898–901 (2005).
doi: 10.1038/nature04033
Papes, F., Logan, D. W. & Stowers, L. The vomeronasal organ mediates interspecies defensive behaviors through detection of protein pheromone homologs. Cell 141, 692–703 (2010).
doi: 10.1016/j.cell.2010.03.037
National Research Council (US) Committee. Guide for the Care and Use of Laboratory Animals (National Academies Press, 2011).
Champlin, A. K. Suppression of oestrus in grouped mice: the effects of various densities and the possible nature of the stimulus. J. Reprod. Fertil. 27, 233–241 (1971).
doi: 10.1530/jrf.0.0270233
Byers, S. L., Wiles, M. V., Dunn, S. L. & Taft, R. A. Mouse estrous cycle identification tool and images. PLoS ONE 7, e35538 (2012).
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Tchernichovski, O., Nottebohm, F., Ho, C. E., Pesaran, B. & Mitra, P. P. A procedure for an automated measurement of song similarity. Anim. Behav. 59, 1167–1176 (2000).
doi: 10.1006/anbe.1999.1416
Van Segbroeck, M., Knoll, A. T., Levitt, P. & Narayanan, S. MUPET—Mouse Ultrasonic Profile ExTraction: a signal processing tool for rapid and unsupervised analysis of ultrasonic vocalizations. Neuron 94, 465–485.e5 (2017).
doi: 10.1016/j.neuron.2017.04.005
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Auteurs

Ebru Demir (E)

Department of Neuroscience, Columbia University, Mortimer B. Zuckerman Mind Brain Behavior Institute, New York, NY, USA.
Department of Neuroscience, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.

Kenneth Li (K)

Department of Neuroscience, Columbia University, Mortimer B. Zuckerman Mind Brain Behavior Institute, New York, NY, USA.

Natasha Bobrowski-Khoury (N)

Department of Neuroscience, Columbia University, Mortimer B. Zuckerman Mind Brain Behavior Institute, New York, NY, USA.
Department of Neuroscience, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.

Joshua I Sanders (JI)

Department of Neuroscience, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.
Sanworks LLC, Stony Brook, NY, USA.

Robert J Beynon (RJ)

Centre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, UK.

Jane L Hurst (JL)

Mammalian Behaviour and Evolution Group, Institute of Integrative Biology, University of Liverpool, Leahurst Campus, Neston, UK.

Adam Kepecs (A)

Department of Neuroscience, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA. akepecs@wustl.edu.
Department of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA. akepecs@wustl.edu.
Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA. akepecs@wustl.edu.

Richard Axel (R)

Department of Neuroscience, Columbia University, Mortimer B. Zuckerman Mind Brain Behavior Institute, New York, NY, USA. ra27@columbia.edu.
Howard Hughes Medical Institute, Columbia University, New York, NY, USA. ra27@columbia.edu.

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