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PLoS Genet


Title:Selection on Coding and Regulatory Variation Maintains Individuality in Major Urinary Protein Scent Marks in Wild Mice
Author(s):Sheehan MJ; Lee V; Corbett-Detig R; Bi K; Beynon RJ; Hurst JL; Nachman MW;
Address:"Neurobiology and Behavior, Cornell University, Ithaca, New York, United States of America. Museum of Vertebrate Zoology, University of California, Berkeley, Berkeley, California, United States of America. Ecology and Evolutionary Biology, University of Arizona, Tucson, Arizona, United States of America. Centre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom. Integrative Biology, University of California, Berkeley, Berkeley, California, United States of America. Computational Genomics Resource Laboratory (CGRL), California Institute for Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, United States of America. Mammalian Behaviour and Evolution Group, Institute of Integrative Biology, University of Liverpool, Leahurst Campus, Neston, United Kingdom"
Journal Title:PLoS Genet
Year:2016
Volume:20160303
Issue:3
Page Number:e1005891 -
DOI: 10.1371/journal.pgen.1005891
ISSN/ISBN:1553-7404 (Electronic) 1553-7390 (Print) 1553-7390 (Linking)
Abstract:"Recognition of individuals by scent is widespread across animal taxa. Though animals can often discriminate chemical blends based on many compounds, recent work shows that specific protein pheromones are necessary and sufficient for individual recognition via scent marks in mice. The genetic nature of individuality in scent marks (e.g. coding versus regulatory variation) and the evolutionary processes that maintain diversity are poorly understood. The individual signatures in scent marks of house mice are the protein products of a group of highly similar paralogs in the major urinary protein (Mup) gene family. Using the offspring of wild-caught mice, we examine individuality in the major urinary protein (MUP) scent marks at the DNA, RNA and protein levels. We show that individuality arises through a combination of variation at amino acid coding sites and differential transcription of central Mup genes across individuals, and we identify eSNPs in promoters. There is no evidence of post-transcriptional processes influencing phenotypic diversity as transcripts accurately predict the relative abundance of proteins in urine samples. The match between transcripts and urine samples taken six months earlier also emphasizes that the proportional relationships across central MUP isoforms in urine is stable. Balancing selection maintains coding variants at moderate frequencies, though pheromone diversity appears limited by interactions with vomeronasal receptors. We find that differential transcription of the central Mup paralogs within and between individuals significantly increases the individuality of pheromone blends. Balancing selection on gene regulation allows for increased individuality via combinatorial diversity in a limited number of pheromones"
Keywords:"Animals Genetic Variation Individuality Mice Open Reading Frames/*genetics Pheromones/*genetics Polymorphism, Single Nucleotide/genetics Proteins/*genetics Regulatory Sequences, Nucleic Acid/*genetics Urine;"
Notes:"MedlineSheehan, Michael J Lee, Victoria Corbett-Detig, Russell Bi, Ke Beynon, Robert J Hurst, Jane L Nachman, Michael W eng F32 GM101863/GM/NIGMS NIH HHS/ R01 GM074245/GM/NIGMS NIH HHS/ BB/J002631/1/BB_/Biotechnology and Biological Sciences Research Council/United Kingdom Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't 2016/03/05 PLoS Genet. 2016 Mar 3; 12(3):e1005891. doi: 10.1371/journal.pgen.1005891. eCollection 2016 Mar"

 
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