Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-19T02:12:22.925Z Has data issue: false hasContentIssue false

The serotonin transporter gene is a substrate for age and stress dependent epigenetic regulation in rhesus macaque brain: Potential roles in genetic selection and Gene × Environment interactions

Published online by Cambridge University Press:  15 October 2012

Stephen G. Lindell
Affiliation:
NIH/NIAAA
Qiaoping Yuan
Affiliation:
NIH/NIAAA
Zhifeng Zhou
Affiliation:
NIH/NIAAA
David Goldman
Affiliation:
NIH/NIAAA
Robert C. Thompson
Affiliation:
University of Michigan
Juan F. Lopez
Affiliation:
University of Michigan
Stephen J. Suomi
Affiliation:
NIH/NICHD
J. Dee Higley
Affiliation:
Brigham Young University
Christina S. Barr*
Affiliation:
NIH/NIAAA
*
Address correspondence and reprint requests to: Christina S. Barr, Section of Comparative Behavioral Genomics, Laboratory of Neurogenetics, DICBR, NIAAA, NIH, 5625 Fishers Lane, Room 3S-32, Rockville, MD 20852; E-mail: [email protected].

Abstract

In humans, it has been demonstrated that the serotonin transporter linked polymorphic region (5-HTTLPR) genotype moderates risk in the face of adversity. One mechanism by which stress could interact with genotype is via epigenetic modifications. We wanted to examine whether stress interacted with genotype to predict binding of a histone 3 protein trimethylated at lysine 3 (H3K4me3) that marks active promoters. The brains (N = 61) of male rhesus macaques that had been reared in the presence or absence of stress were archived and the hippocampusi dissected. Chromatin immunoprecipitation was performed with an antibody against H3K4me3 followed by sequencing on a SolexaG2A. The effects of age, genotype (5-HTTLPR long/long vs. short), and stress exposure (peer-reared vs. mother-reared) on levels of H3K4me3 binding were determined. We found effects of age and stress exposure. There was a decline in H3K4me3 from preadolescence to postadolescence and lower levels in peer-reared monkeys and no effects of genotype. When we controlled for age, however, we found that there were effects of 5-HTTLPR genotype and rearing condition on H3K4me3 binding. In a larger sample, we observed that cerebrospinal fluid 5-hydroxyindoleacetic acid levels were subject to interactive effects among age, rearing history, and genotype. Genes containing both genetic selection and epigenetic regulation may be particularly important in stress adaptation and development. We find evidence for selection at the solute carrier family C6 member 4 gene and observe epigenetic reorganization according to genotype, stress, and age. These data suggest that developmental stage may moderate effects of stress and serotonin transporter genotype in the emergence of alternative adaptation strategies and in the vulnerability to developmental or psychiatric disorders.

Type
Articles
Copyright
Copyright © Cambridge University Press 2012

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adamsen, D., Meili, D., Blau, N., Thony, B., & Ramaekers, V. (2010). Autism associated with low 5-HIAA in CSF and the heterozygous SLC6A4 gene Gly56Ala plus 5-HTTLPR L/L promoter variants. Molecular Genetics, 102, 368373.Google ScholarPubMed
Barr, C. S. (2011). Primate models of alcohol use disorders: Genetic and environmental variables. Unpublished manuscript.Google Scholar
Barr, C. S., Chen, S. A., Schwandt, M. L., Lindell, S. G., Sun, H., Suomi, S. J., et al. (2010). Suppression of alcohol preference by naltrexone in the rhesus macaque: a critical role of genetic variation at the micro-opioid receptor gene locus. Biological Psychiatry, 67, 7880.Google Scholar
Barr, C. S., Dvoskin, R. L., Gupte, M., Sommer, W., Sun, H., Schwandt, M. L., et al. (2009). Functional CRH promoter variation drives stress-induced alcohol consumption in primates. Proceedings of the National Academy of Sciences, 106, 1459314598.Google Scholar
Barr, C. S., & Goldman, D. (2006). Nonhuman primate models of inheritance of vulnerability to alcohol abuse and addiction. Addiction Biology, 11, 374385.CrossRefGoogle Scholar
Barr, C. S., Newman, T. K., Becker, M. L., Parker, C. C., Champoux, M., Lesch, K. P., et al. (2003). The utility of the non-human primate: Model for studying gene by environment interactions in behavioral research. Genes, Brain, and Behavior, 2, 336340.Google Scholar
Barr, C. S., Newman, T. K., Lindell, S., Shannon, C., Champoux, M., Lesch, K. P., et al. (2004). Interaction between serotonin transporter gene variation and rearing condition in alcohol preference and consumption in female primates. Archives of General Psychiatry, 61, 11461152.Google Scholar
Barr, C. S., Newman, T. K., Schwandt, M., Shannon, C., Dvoskin, R. L., Lindell, S. G., et al. (2004). Sexual dichotomy of an interaction between early adversity and the serotonin transporter gene promoter variant in rhesus macaques. Proceedings of the National Academy of Sciences, 101, 1235812363.CrossRefGoogle ScholarPubMed
Barr, C. S., Newman, T. K., Shannon, C., Parker, C. C., Dvoskin, R. L., Becker, M. L., et al. (2004). Rearing condition and rh5-HTTLPR interact to influence limbic–hypothalamic–pituitary–adrenal axis response to stress in infant macaques. Biological Psychiatry, 55, 733738.Google Scholar
Barr, C. S., Schwandt, M. L., Lindell, S. G., Chen, S. A., Suomi, S. J., Goldman, D., et al. (2007). Mu opioid receptor gene variation is associated with alcohol response and consumption in rhesus monkeys. Archives of General Psychiatry, 64, 369376.CrossRefGoogle Scholar
Barr, C. S., Schwandt, M. L., Lindell, S. G., Higley, J. D., Maestripieri, D., Goldman, D., et al. (2008). A functional OPRM1 variant is associated with attachment behavior in infant rhesus macaques. Proceedings of the National Academy of Sciences, 105, 52775281.Google Scholar
Barr, C. S., Schwandt, M., Newman, T. K., & Higley, J. D. (2004). The use of adolescent nonhuman primates to model human alcohol intake: Neurobiological, genetic and environmental variables. Annals of the New York Academy of Sciences, 1021, 221233.Google Scholar
Bennett, A. J., Lesch, K.-P., Heils, A., Long, J. C., Lorenz, J. G., Shoaf, S. E., et al. (2002). Early experience and serotonin transporter gene variation interact to influence primate CNS function. Molecular Psychiatry, 7, 118122.CrossRefGoogle ScholarPubMed
Bethea, C. L., Streicher, J. M., Coleman, K., Pau, F. K. Y., Moessner, R., & Cameron, J. L. (2004). Anxious behavior and fenfluramine-induced prolactin secretion in young rhesus macaques with different alleles of the serotonin reuptake transporter polymorphism (5HTTLPR). Behavior Genetics, 34, 295307.Google Scholar
Caspi, A., Hariri, A. R., Holmes, A., Uher, R., & Moffitt, T. E. (2010). Genetic sensitivity to the environment; the case of the serotonin transporter gene and its implications for studying complex diseases and traits. American Journal of Psychiatry, 167, 509527.Google Scholar
Caspi, A., Sugden, K., Moffitt, T. E., Taylor, A., Craig, I. W., Harrington, H., et al. (2003). Influence of life stress on depression: Moderation by a polymorphism in the 5-HTT gene. Science, 301, 386389.Google Scholar
Chamove, A. S., Rosenblum, L. A., & Harlow, H. F. (1973). Monkeys (Macaca mulatta) raised only with peers. Animal Behavior, 21, 316325.Google Scholar
Champoux, M., Bennett, A., Shannon, C., Higley, J. D., Lesch, K. P., & Suomi, S. J. (2002). Serotonin transporter gene polymorphism, differential early rearing, and behavior in rhesus monkey neonates. Molecular Psychiatry, 7, 10581063.Google Scholar
Copeland, W. E., Sun, H., Costello, E. J., Angold, A., Heilig, M. A., & Barr, C. S. (2011). Child–opioid receptor gene variant influences parent–child relations. Neuropsychopharmacology, 36, 11651170.CrossRefGoogle ScholarPubMed
Crockett, M. J., Clark, L., Hauser, M. D., & Robbins, T. W. (2010). Serotonin selectively influences moral judgment and behavior through effects on harm aversion. Proceedings of the National Academy of Sciences, 107, 1743317438.Google Scholar
Harlow, H. F., & Suomi, S. J. (1974). Induced depression in monkeys. Behavioral Biology, 12, 273296.Google Scholar
Heinz, A. J., Beck, A., Meyer-Lindenberg, A., Sterzer, P., & Heinz, A. (2011). Cognitive and neurobiological mechanisms of alcohol-related aggression. Nature Reviews in Neuroscience, 12, 400413.CrossRefGoogle ScholarPubMed
Herman, A. I., Conner, T. S., Anton, R. F., Gelernter, J., Kranzler, H. R., & Covault, J. (2011). Variation in the gene encoding the serotonin transporter is associated with a measure of sociopathy in alcoholics. Addiction Biology, 16, 124132.Google Scholar
Higley, J. D., Hasert, M. F., Suomi, S. J., & Linnoila, M. (1991). Nonhuman primate model of alcohol abuse: Effects of early experience, personality, and stress on alcohol consumption. Proceedings of the National Academy of Sciences, 88, 72617265.CrossRefGoogle ScholarPubMed
Higley, J. D., Suomi, S. J., & Linnoila, M. (1996). A nonhuman primate model of type II excessive alcohol consumption? Part 1. Low cerebrospinal fluid 5-hydroxyindoleacetic acid concentrations and diminished social competence correlate with excessive alcohol consumption. Alcoholism: Clinical and Experimental Research, 20, 629642.Google Scholar
Homberg, J. R., & Lesch, K. P. (2011). Looking on the bright side of serotonin transporter gene variation. Biological Psychiatry, 69, 513519.Google Scholar
Hu, X. Z., Lipsky, R. H., Zhu, G., Akhtar, L. A., Taubman, J., Greenberg, B. D., et al. (2006). Serotonin transporter promoter gain-of-function genotypes are linked to obsessive–compulsive disorder. American Journal of Human Genetics, 78, 815826.Google Scholar
Karg, K., Burmeister, M., Shedden, K., & Sen, S. (2011). The serotonin transporter promoter polymorphism (5-HTTLPR), stress and depression meta-analysis revisited. Archives of General Psychiatry, 68, 444454.Google Scholar
Kinnally, E. L., Capitanio, J. P., Leibel, R., Deng, L., Leduc, C., Haghighi, F., et al. (2010). Epigenetic regulation of serotonin transporter expression and behavior in infant rhesus macaques. Genes, Brain, and Behavior, 9, 575582.CrossRefGoogle ScholarPubMed
Korte, S. M., Koolhaas, J. M., Wingfield, J. C., & McEwen, B. S. (2005). The Darwinian concept of stress: benefits of allostasis and costs of allostatic load and the tradeoffs in health and disease. Neuroscience & Biobehavioral Reviews, 29, 338.Google Scholar
Kraemer, G. W., Moore, C. F., Newman, T. K., Barr, C. S., & Schneider, M. L. (2008). Moderate levels of fetal alcohol exposure and serotonin transporter gene promoter polymorphism affect neonatal temperament and LHPA axis regulation in monkeys. Biological Psychiatry, 63, 317324.Google Scholar
Krawczak, M., Trefilov, A., Berard, J., Bercovitch, F., Kessler, M., Sauermann, U., et al. (2005). Male reproductive timing in rhesus macaques is influenced by the HTTLPR promoter polymorphism of the serotonin transporter gene. Biology of Reproduction, 72, 11091113.CrossRefGoogle Scholar
Lesch, K. P., Meyer, J., Glatz, K., Flügge, G., Hinney, A., Hebebrand, J., et al. (1997). The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: Alternative biallelic variation in rhesus monkeys. Journal of Neural Transmission, 104, 12591266.CrossRefGoogle ScholarPubMed
Lin, E., Chen, P. S., Chang, H. H., Gean, P.-W., Tsai, H. C., Yang, Y. K., et al. (2009). Interaction of serotonin-related genes affects short-term antidepressant response in major depressive disorder. Progress in Neuropsychopharmacology and Biological Psychiatry, 33, 11671172.Google Scholar
Lindell, S. G., Schwandt, M. L., Sun, H., Sparenborg, J. D., Bjoerk, K., Kasckow, J. W., et al. (2010). Functional NPY variation as a factor in stress resilience in rhesus macaques. Archives of General Psychiatry, 67, 423431.Google Scholar
Lopez, J. F., & Higley, J. D. (2002). The effect of early experience on brain corticosteroid and serotonin receptors in rhesus monkeys. Biological Psychiatry, 51, 294.Google Scholar
Mazzanti, C. M., Lappalainen, J., Long, J. C., Bengel, D., Naukkarinen, H., Eggert, M., et al. (1998). Role of the serotonin transporter promoter polymorphism in anxiety-related traits. Archives of General Psychiatry, 55, 936940.Google Scholar
McEwen, B. S. (2006). Protective and damaging effects of stress mediators: Central role of the brain. Dialogues in Clinical Neuroscience, 8, 367381.Google Scholar
Neigh, G. N., Gillespie, C. F., & Nemeroff, C. B. (2009). The neurobiological toll of child abuse and neglect. Trauma Violence Abuse, 10, 389410.CrossRefGoogle ScholarPubMed
Risch, N., Herrell, R., Lehner, T., Liang, K. Y., Eaves, L., Hoh, J., et al. (2009). Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: A meta-analysis. Journal of the American Medical Association, 301, 24622471.Google Scholar
Schwandt, M. L., Lindell, S. G., Sjoberg, R. L., Chisholm, K. L., Higley, J. D., Suomi, S. J., et al. (2010). Gene–environment interactions and response to social intrusion in male and female rhesus macaques. Biological Psychiatry, 67, 323330.Google Scholar
Sinha, R. (2007). Chronic stress, drug use, and vulnerability to addiction. Annals of the New York Academy of Sciences, 1141, 105130.CrossRefGoogle Scholar
Smith, M. J., & Price, G. R. (1973). The logic of animal conflict. Nature, 246, 1518.Google Scholar
Spinelli, S., Chefer, S., Carson, R. E., Jagoda, E., Lang, L., Heilig, M., et al. (2010). Effects of early-life stress on serotonin 1A receptors in juvenile rhesus monkeys measured by PET. Biologial Psychiatry, 67, 11461153.CrossRefGoogle Scholar
Spinelli, S., Chefer, S., Suomi, S. J., Higley, J. D., Barr, C. S., & Stein, E. (2009). Early life stress induces long-term morphologic changes in primate brain. Archives of General Psychiatry, 66, 658665.Google Scholar
Spinelli, S., Schwandt, M. L., Lindell, S. G., Heilig, M., Suomi, S. J., Higley, J. D., et al. (2012). The serotonin transporter gene linked polymorphic region is associated with the behavioral response to repeated stress exposure in infant rhesus macaques. Development and Psychopathology, 24, 157165.Google Scholar
Spinelli, S., Schwandt, M. L., Lindell, S. G., Newman, T. K., Heilig, M., Higley, J. D., et al. (2007). Association between the rh-5HTTLPR polymorphism and behavior in rhesus macaques during social separation stress. Developmental Psychopathology, 19, 977987.Google Scholar
Suomi, S. J. (1982). Abnormal behavior in nonhuman primates. In Fobes, J. D. & King, J. E. (Eds.), Primate behavior. New York: Academic Press.Google Scholar
Veenstra-Vanderweele, J., Jessen, T. N., Thompson, B. J., Carter, M., Prasad, H. C., Steiner, J. A., et al. (2009). Modeling rare gene variation to gain insight into the oldest biomarker in autism: Construction of the serotonin transporter Gly56Als knock-in mouse. Journal of Neurodevelopmental Disorders, 1, 158171.Google Scholar
Wendland, J. R., Lesch, K. P., Newman, T. K., Timme, A., Gachot-Neveu, H., Thierry, B., et al. (2005). Differential functional variability of serotonin transporter and monoamine oxidase A genes in macaque species displaying contrasting levels of aggression-related behavior. Behavior Genetics, 30, 110.Google Scholar
Yuan, Q., Zhou, Z., Lindell, S. G., Higley, J. D., Ferguson, E., Thompson, R. C., et al. (2012). The rhesus macaque is three times as diverse but more closely equivalent in “damaging” coding variation as compared to the human. BMC Genetics, 13, 52.Google Scholar
Supplementary material: Image

Lindell et al. supplementary material

Supplementary figure

Download Lindell et al. supplementary material(Image)
Image 370.8 KB
Supplementary material: Image

Lindell et al. supplementary material

Supplementary figure

Download Lindell et al. supplementary material(Image)
Image 425.9 KB