Associations between Dopamine D4 Receptor Gene Variation with Both Infidelity and Sexual Promiscuity

Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary theory (sexual selection), little is known about the genetic bases of individual variation in sexual behavior. The variable number tandem re...

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Published inPloS one Vol. 5; no. 11; p. e14162
Main Authors Garcia, Justin R., MacKillop, James, Aller, Edward L., Merriwether, Ann M., Wilson, David Sloan, Lum, J. Koji
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 30.11.2010
Public Library of Science (PLoS)
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Online AccessGet full text
ISSN1932-6203
1932-6203
DOI10.1371/journal.pone.0014162

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Abstract Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary theory (sexual selection), little is known about the genetic bases of individual variation in sexual behavior. The variable number tandem repeats (VNTR) polymorphism in exon III of the human dopamine D4 receptor gene (DRD4) has been correlated with an array of behavioral phenotypes and may be predicatively responsible for variation in motivating some sexual behaviors, particularly promiscuity and infidelity. We administered an anonymous survey on personal history of sexual behavior and intimate relationships to 181 young adults. We also collected buccal wash samples and genotyped the DRD4 VNTR. Here we show that individuals with at least one 7-repeat allele (7R+) report a greater categorical rate of promiscuous sexual behavior (i.e., having ever had a "one-night stand") and report a more than 50% increase in instances of sexual infidelity. DRD4 VNTR genotype varies considerably within and among populations and has been subject to relatively recent, local selective pressures. Individual differences in sexual behavior are likely partially mediated by individual genetic variation in genes coding for motivation and reward in the brain. Conceptualizing these findings in terms of r/K selection theory suggests a mechanism for selective pressure for and against the 7R+ genotype that may explain the considerable global allelic variation for this polymorphism.
AbstractList Background Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary theory (sexual selection), little is known about the genetic bases of individual variation in sexual behavior. The variable number tandem repeats (VNTR) polymorphism in exon III of the human dopamine D4 receptor gene (DRD4) has been correlated with an array of behavioral phenotypes and may be predicatively responsible for variation in motivating some sexual behaviors, particularly promiscuity and infidelity. Methodology/Principal Findings We administered an anonymous survey on personal history of sexual behavior and intimate relationships to 181 young adults. We also collected buccal wash samples and genotyped the DRD4 VNTR. Here we show that individuals with at least one 7-repeat allele (7R+) report a greater categorical rate of promiscuous sexual behavior (i.e., having ever had a "one-night stand") and report a more than 50% increase in instances of sexual infidelity. Conclusions/Significance DRD4 VNTR genotype varies considerably within and among populations and has been subject to relatively recent, local selective pressures. Individual differences in sexual behavior are likely partially mediated by individual genetic variation in genes coding for motivation and reward in the brain. Conceptualizing these findings in terms of r/K selection theory suggests a mechanism for selective pressure for and against the 7R+ genotype that may explain the considerable global allelic variation for this polymorphism.
Background Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary theory (sexual selection), little is known about the genetic bases of individual variation in sexual behavior. The variable number tandem repeats (VNTR) polymorphism in exon III of the human dopamine D4 receptor gene (DRD4) has been correlated with an array of behavioral phenotypes and may be predicatively responsible for variation in motivating some sexual behaviors, particularly promiscuity and infidelity. Methodology/Principal Findings We administered an anonymous survey on personal history of sexual behavior and intimate relationships to 181 young adults. We also collected buccal wash samples and genotyped the DRD4 VNTR. Here we show that individuals with at least one 7-repeat allele (7R+) report a greater categorical rate of promiscuous sexual behavior (i.e., having ever had a “one-night stand”) and report a more than 50% increase in instances of sexual infidelity. Conclusions/Significance DRD4 VNTR genotype varies considerably within and among populations and has been subject to relatively recent, local selective pressures. Individual differences in sexual behavior are likely partially mediated by individual genetic variation in genes coding for motivation and reward in the brain. Conceptualizing these findings in terms of r/K selection theory suggests a mechanism for selective pressure for and against the 7R+ genotype that may explain the considerable global allelic variation for this polymorphism.
Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary theory (sexual selection), little is known about the genetic bases of individual variation in sexual behavior. The variable number tandem repeats (VNTR) polymorphism in exon III of the human dopamine D4 receptor gene (DRD4) has been correlated with an array of behavioral phenotypes and may be predicatively responsible for variation in motivating some sexual behaviors, particularly promiscuity and infidelity. We administered an anonymous survey on personal history of sexual behavior and intimate relationships to 181 young adults. We also collected buccal wash samples and genotyped the DRD4 VNTR. Here we show that individuals with at least one 7-repeat allele (7R+) report a greater categorical rate of promiscuous sexual behavior (i.e., having ever had a "one-night stand") and report a more than 50% increase in instances of sexual infidelity. DRD4 VNTR genotype varies considerably within and among populations and has been subject to relatively recent, local selective pressures. Individual differences in sexual behavior are likely partially mediated by individual genetic variation in genes coding for motivation and reward in the brain. Conceptualizing these findings in terms of r/K selection theory suggests a mechanism for selective pressure for and against the 7R+ genotype that may explain the considerable global allelic variation for this polymorphism.
Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary theory (sexual selection), little is known about the genetic bases of individual variation in sexual behavior. The variable number tandem repeats (VNTR) polymorphism in exon III of the human dopamine D4 receptor gene (DRD4) has been correlated with an array of behavioral phenotypes and may be predicatively responsible for variation in motivating some sexual behaviors, particularly promiscuity and infidelity. We administered an anonymous survey on personal history of sexual behavior and intimate relationships to 181 young adults. We also collected buccal wash samples and genotyped the DRD4 VNTR. Here we show that individuals with at least one 7-repeat allele (7R+) report a greater categorical rate of promiscuous sexual behavior (i.e., having ever had a "one-night stand") and report a more than 50% increase in instances of sexual infidelity. DRD4 VNTR genotype varies considerably within and among populations and has been subject to relatively recent, local selective pressures. Individual differences in sexual behavior are likely partially mediated by individual genetic variation in genes coding for motivation and reward in the brain. Conceptualizing these findings in terms of r/K selection theory suggests a mechanism for selective pressure for and against the 7R+ genotype that may explain the considerable global allelic variation for this polymorphism.
Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary theory (sexual selection), little is known about the genetic bases of individual variation in sexual behavior. The variable number tandem repeats (VNTR) polymorphism in exon III of the human dopamine D4 receptor gene (DRD4) has been correlated with an array of behavioral phenotypes and may be predicatively responsible for variation in motivating some sexual behaviors, particularly promiscuity and infidelity.BACKGROUNDHuman sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary theory (sexual selection), little is known about the genetic bases of individual variation in sexual behavior. The variable number tandem repeats (VNTR) polymorphism in exon III of the human dopamine D4 receptor gene (DRD4) has been correlated with an array of behavioral phenotypes and may be predicatively responsible for variation in motivating some sexual behaviors, particularly promiscuity and infidelity.We administered an anonymous survey on personal history of sexual behavior and intimate relationships to 181 young adults. We also collected buccal wash samples and genotyped the DRD4 VNTR. Here we show that individuals with at least one 7-repeat allele (7R+) report a greater categorical rate of promiscuous sexual behavior (i.e., having ever had a "one-night stand") and report a more than 50% increase in instances of sexual infidelity.METHODOLOGY/PRINCIPAL FINDINGSWe administered an anonymous survey on personal history of sexual behavior and intimate relationships to 181 young adults. We also collected buccal wash samples and genotyped the DRD4 VNTR. Here we show that individuals with at least one 7-repeat allele (7R+) report a greater categorical rate of promiscuous sexual behavior (i.e., having ever had a "one-night stand") and report a more than 50% increase in instances of sexual infidelity.DRD4 VNTR genotype varies considerably within and among populations and has been subject to relatively recent, local selective pressures. Individual differences in sexual behavior are likely partially mediated by individual genetic variation in genes coding for motivation and reward in the brain. Conceptualizing these findings in terms of r/K selection theory suggests a mechanism for selective pressure for and against the 7R+ genotype that may explain the considerable global allelic variation for this polymorphism.CONCLUSIONS/SIGNIFICANCEDRD4 VNTR genotype varies considerably within and among populations and has been subject to relatively recent, local selective pressures. Individual differences in sexual behavior are likely partially mediated by individual genetic variation in genes coding for motivation and reward in the brain. Conceptualizing these findings in terms of r/K selection theory suggests a mechanism for selective pressure for and against the 7R+ genotype that may explain the considerable global allelic variation for this polymorphism.
Audience Academic
Author Aller, Edward L.
Garcia, Justin R.
Wilson, David Sloan
Lum, J. Koji
Merriwether, Ann M.
MacKillop, James
AuthorAffiliation 5 Department of Psychology, University of Georgia, Athens, Georgia, United States of America
Kyushu University, Japan
7 Department of Psychology, Binghamton University, Binghamton, New York, United States of America
8 Department of Human Development, Binghamton University, Binghamton, New York, United States of America
6 Center for Alcohol and Addiction Studies, Brown University, Providence, Rhode Island, United States of America
1 Laboratory of Evolutionary Anthropology and Health, Binghamton University, Binghamton, New York, United States of America
3 Department of Anthropology, Binghamton University, Binghamton, New York, United States of America
2 Department of Biological Sciences, Binghamton University, Binghamton, New York, United States of America
4 Institute for Evolutionary Studies, Binghamton University, Binghamton, New York, United States of America
AuthorAffiliation_xml – name: 4 Institute for Evolutionary Studies, Binghamton University, Binghamton, New York, United States of America
– name: 5 Department of Psychology, University of Georgia, Athens, Georgia, United States of America
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– name: 8 Department of Human Development, Binghamton University, Binghamton, New York, United States of America
– name: 1 Laboratory of Evolutionary Anthropology and Health, Binghamton University, Binghamton, New York, United States of America
– name: 6 Center for Alcohol and Addiction Studies, Brown University, Providence, Rhode Island, United States of America
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– name: 7 Department of Psychology, Binghamton University, Binghamton, New York, United States of America
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  givenname: Justin R.
  surname: Garcia
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  givenname: David Sloan
  surname: Wilson
  fullname: Wilson, David Sloan
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  givenname: J. Koji
  surname: Lum
  fullname: Lum, J. Koji
BackLink https://www.ncbi.nlm.nih.gov/pubmed/21152404$$D View this record in MEDLINE/PubMed
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2010 Garcia et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Garcia et al. 2010
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– notice: 2010 Garcia et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: Garcia et al. 2010
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Issue 11
Language English
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Conceived and designed the experiments: JRG AMM DSW JKKL. Performed the experiments: JRG ELA. Analyzed the data: JRG JM. Contributed reagents/materials/analysis tools: JKKL. Wrote the paper: JRG JM.
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References_xml – reference: 17186131 - Arch Sex Behav. 2007 Aug;36(4):543-54
– reference: 7770195 - Neurosci Biobehav Rev. 1995 Spring;19(1):19-38
– reference: 14581929 - Pharmacogenomics J. 2003;3(6):343-8
– reference: 18765804 - Proc Natl Acad Sci U S A. 2008 Sep 16;105(37):14153-6
– reference: 12406233 - Mol Ecol. 2002 Nov;11(11):2195-212
– reference: 18715282 - Addict Biol. 2009 Apr;14(2):238-44
– reference: 16209725 - Behav Brain Sci. 2005 Jun;28(3):313-50; discussion 350-95
– reference: 11535555 - Cancer Epidemiol Biomarkers Prev. 2001 Sep;10(9):1005-8
– reference: 16774975 - Hum Mol Genet. 2006 Jul 15;15(14):2276-84
– reference: 15662148 - J Child Adolesc Psychopharmacol. 2004 Winter;14(4):564-74
– reference: 17309802 - Behav Brain Funct. 2007 Feb 19;3:11
– reference: 8483982 - Psychol Rev. 1993 Apr;100(2):204-32
– reference: 1932883 - Br J Addict. 1991 Sep;86(9):1119-27
– reference: 10673763 - Mol Psychiatry. 2000 Jan;5(1):11-3
– reference: 9924738 - Psychoneuroendocrinology. 1998 Nov;23(8):779-818
– reference: 12238608 - Arch Sex Behav. 2002 Oct;31(5):413-9
– reference: 15053706 - J Pers Soc Psychol. 2004 Apr;86(4):560-84
– reference: 19813084 - Behav Genet. 2010 Jan;40(1):12-21
– reference: 11756666 - Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):309-14
– reference: 11252992 - Nat Rev Neurosci. 2001 Feb;2(2):129-36
– reference: 15607016 - Twin Res. 2004 Dec;7(6):649-58
– reference: 16216685 - Brain Res Bull. 2005 Nov 15;67(5):391-7
– reference: 16619053 - Mol Psychiatry. 2006 Aug;11(8):782-6
– reference: 11782544 - Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):10-2
– reference: 17525955 - Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):27-32
– reference: 10100392 - J Exp Psychol Gen. 1999 Mar;128(1):78-87
– reference: 16327783 - Nat Neurosci. 2006 Jan;9(1):133-9
– reference: 17245411 - Eur J Hum Genet. 2007 Mar;15(3):279-87
– reference: 15077199 - Am J Hum Genet. 2004 May;74(5):931-44
– reference: 19713452 - Soc Cogn Affect Neurosci. 2010 Jun;5(2-3):194-202
– reference: 19336242 - Pharmacol Biochem Behav. 2009 Sep;93(3):222-9
– reference: 8186185 - Violence Vict. 1993 Fall;8(3):271-94
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Snippet Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to evolutionary...
Background Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to...
Background Human sexual behavior is highly variable both within and between populations. While sex-related characteristics and sexual behavior are central to...
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SubjectTerms Adults
Animal behavior
Attention deficit hyperactivity disorder
Biological evolution
Brain
Coding
Discount rates
Dopamine
Dopamine D4 receptors
Dopamine receptors
Evolution (Biology)
Evolutionary Biology/Human Evolution
Evolutionary Biology/Sexual Behavior
Female
Gene polymorphism
Genes
Genetic aspects
Genetic diversity
Genetic polymorphisms
Genotype
Human behavior
Humans
Linear Models
Male
Minisatellite Repeats - genetics
Motivation
Neural coding
Neuroscience/Behavioral Neuroscience
Phenols (Class of compounds)
Polymorphism
Polymorphism, Genetic
Populations
Promiscuity
Receptors, Dopamine D4 - genetics
Reinforcement
Reward
Sex Factors
Sexual Behavior
Sexual selection
Smoking
Statistics, Nonparametric
Surveys and Questionnaires
Young Adult
Young adults
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Title Associations between Dopamine D4 Receptor Gene Variation with Both Infidelity and Sexual Promiscuity
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