Your browser doesn't support javascript.
loading
Early rearing history influences oxytocin receptor epigenetic regulation in rhesus macaques.
Baker, Maggie; Lindell, Stephen G; Driscoll, Carlos A; Zhou, Zhifeng; Yuan, Qiaoping; Schwandt, Melanie L; Miller-Crews, Isaac; Simpson, Elizabeth A; Paukner, Annika; Ferrari, Pier Francesco; Sindhu, Ravi Kumar; Razaqyar, Muslima; Sommer, Wolfgang H; Lopez, Juan F; Thompson, Robert C; Goldman, David; Heilig, Markus; Higley, J Dee; Suomi, Stephen J; Barr, Christina S.
Afiliação
  • Baker M; Section of Comparative Behavioral Genomics, National Institute on Alcohol Abuse and Alcoholism, NIH, Rockville, MD 20852.
  • Lindell SG; Section of Comparative Behavioral Genomics, National Institute on Alcohol Abuse and Alcoholism, NIH, Rockville, MD 20852.
  • Driscoll CA; Laboratory of Clinical Studies, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD 20892.
  • Zhou Z; Section of Comparative Behavioral Genomics, National Institute on Alcohol Abuse and Alcoholism, NIH, Rockville, MD 20852.
  • Yuan Q; Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD 20892.
  • Schwandt ML; Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD 20892.
  • Miller-Crews I; Laboratory of Clinical Studies, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD 20892.
  • Simpson EA; Section of Comparative Behavioral Genomics, National Institute on Alcohol Abuse and Alcoholism, NIH, Rockville, MD 20852.
  • Paukner A; Section of Comparative Ethology, Eunice Shriver Kennedy National Institute of Child Health and Human Development, NIH, Poolesville, MD 20837.
  • Ferrari PF; Section of Comparative Ethology, Eunice Shriver Kennedy National Institute of Child Health and Human Development, NIH, Poolesville, MD 20837.
  • Sindhu RK; Institute des Sciences Cognitives Mar Jeannerod, CNRS, Université Claude Bernard Lyon, 69675 Bron Cedex, France.
  • Razaqyar M; Section of Comparative Behavioral Genomics, National Institute on Alcohol Abuse and Alcoholism, NIH, Rockville, MD 20852.
  • Sommer WH; Section of Comparative Behavioral Genomics, National Institute on Alcohol Abuse and Alcoholism, NIH, Rockville, MD 20852.
  • Lopez JF; Department of Psychopharmacology, Central Institute of Mental Health, Heidelberg University, 68159 Mannheim, Germany.
  • Thompson RC; Department of Addiction Medicine, Central Institute of Mental Health, Heidelberg University, 68159 Mannheim, Germany.
  • Goldman D; Department of Psychiatry, University of Michigan Medical School, Ann Arbor, MI 48109.
  • Heilig M; Department of Psychiatry, University of Michigan Medical School, Ann Arbor, MI 48109.
  • Higley JD; Laboratory of Clinical Studies, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD 20892.
  • Suomi SJ; Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, NIH, Bethesda, MD 20892.
  • Barr CS; Center for Social and Affective Neuroscience, Department of Clinical and Experimental Medicine, Linköping University, S-58183 Linköping, Sweden.
Proc Natl Acad Sci U S A ; 114(44): 11769-11774, 2017 10 31.
Article em En | MEDLINE | ID: mdl-29078292
ABSTRACT
Adaptations to stress can occur through epigenetic processes and may be a conduit for informing offspring of environmental challenge. We employed ChIP-sequencing for H3K4me3 to examine effects of early maternal deprivation (peer-rearing, PR) in archived rhesus macaque hippocampal samples (male, n = 13). Focusing on genes with roles in stress response and behavior, we assessed the effects of rearing on H3K4me3 binding by ANOVA. We found decreased H3K4me3 binding at genes critical to behavioral stress response, the most robust being the oxytocin receptor gene OXTR, for which we observed a corresponding decrease in RNA expression. Based on this finding, we performed behavioral analyses to determine whether a gain-of-function nonsynonymous OXTR SNP interacted with early stress to influence relevant behavioral stress reactivity phenotypes (n = 194), revealing that this SNP partially rescued the PR phenotype. PR infants exhibited higher levels of separation anxiety and arousal in response to social separation, but infants carrying the alternative OXTR allele did not exhibit as great a separation response. These data indicate that the oxytocin system is involved in social-separation response and suggest that epigenetic down-modulation of OXTR could contribute to behavioral differences observed in PR animals. Epigenetic changes at OXTR may represent predictive adaptive responses that could impart readiness to respond to environmental challenge or maintain proximity to a caregiver but also contribute to behavioral pathology. Our data also demonstrate that OXTR polymorphism can permit animals to partially overcome the detrimental effects of early maternal deprivation, which could have translational implications for human psychiatric disorders.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Ocitocina / Epigênese Genética / Macaca mulatta Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Ocitocina / Epigênese Genética / Macaca mulatta Idioma: En Ano de publicação: 2017 Tipo de documento: Article