The influence of genomic imprinting on brain development and behavior

Evolution and Human Behavior

Volumn 22, Issue 6, 2001, Pages 385-407

  Goos, Lisa M ^a   Silverman, Irwin ^a  

^a YORK UNIVERSITY   (Canada)

Author keywords

Behavior; Brain; Development; Genetic conflict; Genetic disorders; Genomic imprinting; Inheritance

Indexed keywords

EID: 0037960519     PISSN: 10905138     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1090-5138(01)00076-9     Document Type: Article

References (89)

1. Abel E.L. Paternal and maternal alcohol consumption: effects on offspring in two strains of rats. Alcohol Clinical and Experimental Research. 13:1989;533-541.
2. Abel E.L., Lee J.A. Paternal alcohol exposure affects offspring behavior but not body or organ weights in mice. Alcohol Clinical and Experimental Research. 12:1988;349-355.
3. Allen N.D., Logan K., Lally G., Drage D.J., Norris M.L., Keverne E.B. Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior. Proceedings of the National Academy of Sciences. 92:1995;10782-10786.
4. Ashton G.C., Borecki I.B. Further evidence for a gene influencing spatial ability. Behavior Genetics. 17:1987;243-256.
5. Attaix D., Combaret L., Pouch M.N., Taillandier D. Regulation of proteolysis. Current Opinion in Clinical Nutrition and Metabolic Care. 4:2001;45-49.
6. Bartolomei M.S., Tilghman S.M. Genomic imprinting in mammals. Annual Review of Genetics. 31:1997;493-525.
7. Barton S.C., Ferguson-Smith A.C., Fundele R., Surani M.A. Influence of paternally imprinted genes on development. Development. 113:1991;679-688.
8. Barton S.C., Surani M.A.H., Norris M.L. Role of paternal and maternal genomes in mouse development. Nature. 311:1984;374-376.
9. Burt A. Textbook of neuroanatomy. 1993;Saunders, Philadelphia.
10. Buss D. Evolutionary psychology. The new science of the mind. 1999;Allyn and Bacon, Boston.
11. Butler M. Prader-Willi Syndrome: current understanding of cause and diagnosis. American Journal of Medical Genetics. 35:1990;319-332.
12. Cavaillé J., Buiting K., Kiefmann M., Lalande M., Brannan C.I., Horsthemke B., Bachellerie J.P., Brosius J., Hüttenhofer A. Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proceedings of the National Academy of Sciences. 97:2000;14311-14316.
13. Ciechanover A., Orian A., Schwartz A.L. Ubiquitin-mediated proteolysis: biological regulation via destruction. BioEssays. 22:2000;442-451.
14. Ciechanover A., Orian A., Schwartz A.L. The ubiquitin-mediated proteolytic pathway: mode of action and clinical implications. Journal of Cellular Biochemistry Supplement. 34:2000;40-51.
15. Cook E.H., Lindgren V., Leventhal B.L., Courchesne R., Lincoln A., Shulman C., Lord C., Courchesne E. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. American Journal of Human Genetics. 60:1997;928-934.
16. Dawson W.D. Fertility and size inheritance in a Peromyscus species cross. Evolution. 19:1965;44-55.
17. Durcan M.J., Goldman D. Genomic imprinting: implications for behavioral genetics. Behavior Genetics. 23:1993;137-143.
18. Falls J.G., Pulford D.J., Wylie A.A., Jirtle R.L. Genomic imprinting: implications for human disease. American Journal of Pathology. 154:1999;635-647.
19. Feinberg A.P. Genomic imprinting and gene activation in cancer. Nature Genetics. 4:1993;110-113.
20. Filipowicz W. Imprinted expression of small nucleolar RNAs in brain: time for RNomics. Proceedings of the National Academy of Sciences. 97:2000;14035-14037.
21. Fleming A.S., Rosenblatt J.S. Olfactory regulation of maternal behavior in rats: I. Effects of olfactory bulb removal in experienced and inexperienced lactating and cycling females. Journal of Comparative and Physiological Psychology. 86:1974;221-232.
22. Fleming A.S., Rosenblatt J.S. Olfactory regulation of maternal behavior in rats: II. Effects of peripherally induced anosmia and lesions of the lateral olfactory tract in pup-induced virgins. Journal of Comparative and Physiological Psychology. 86:1974;233-246.
23. Flint J. Implications of genomic imprinting for psychiatric genetics. Psychological Medicine. 22:1992;5-10.
24. Friend W.C. Psychopathology and nonmendelian inheritance. Seeman M.V. Gender and psychopathology. 1995;41-61 American Psychiatric Press, Washington.
25. Fundele R., Barton S.C., Christ B., Krause R., Surani M.A. Distribution of androgenetic cells in fetal mouse chimeras. Roux's Archive of Developmental Biology. 204:1995;484-493.
26. Fundele R.H., Norris M.L., Barton S.C., Fehlau M., Howlett S.K., Mills W.E., Surani M.A. Temporal and spatial selection against parthenogenetic cells during development of fetal chimeras. Development. 108:1990;203-211.
27. Goshen R., Ben-Rafael Z., Gonik B., Lustig O., Tannos V., de-Groot N., Hochberg A.A. The role of genomic imprinting in implantation. Fertility and Sterility. 62:1994;903-910.
28. Haig D. Genetic conflicts in human pregnancy. The Quarterly Review of Biology. 68:1993;495-532.
29. Haig D. Parental antagonism, relatedness asymmetries, and genomic imprinting. Proceedings of the Royal Society of London, B. 264:1997;1657-1662.
30. Haig D. The divided self. 13th Biannual Meeting of the International Society for Human Ethology, Vancouver, British Columbia, Canada:1998, June.
31. Haig D. Genetic conflicts and the private life of Peromyscus polionotus. Nature Genetics. 22:1999;131.
32. Haig D. Genomic imprinting, sex-biased dispersal, and social behavior. Annals of the New York Academy of Sciences. 907:2000;149-163.
33. Haig D., Graham C. Genomic imprinting and the strange case of the insulin-like growth factor II receptor. Cell. 64:1991;1045-1046.
34. Haig D., Trivers R. The evolution of parental imprinting: a review of hypotheses. Ohlsson R., Hall K., Ritzen M. Genomic imprinting: causes and consequences. 1995;17-28 Cambridge Univ. Press, Cambridge, UK.
35. Haig D., Westoby M. Parent specific gene expression and the triploid endosperm. American Naturalist. 134:1989;147-155.
36. Halford J.C., Blundell J.E. Separate systems for serotonin and leptin in appetite control. Annals of Medicine. 32:2000;222-232.
37. Hall J.G. Genomic imprinting: nature and clinical relevance. Annual Review of Medicine. 48:1997;35-44.
38. Hinde R.A. Can nonhuman primates help us understand human behavior? Smuts B.B., Cheney D.L., Seyfarth R.M., Wrangham R.W., Struhsaker T.T. Primate societies. 1987;413-420 University of Chicago Press, Chicago.
39. 1C receptor mRNA in adult rat brain. FEBS Letters. 247:1989;453-462.
40. Hole J.W. Jr. Human anatomy and physiology. 1984;Wm.C. Brown, Dubuque, IA.
41. Hurst L.D. Evolutionary theories of genomic imprinting. Reik W., Surani A. Genomic imprinting. 1997;211-238 IRL Press, New York.
42. Hurst L.D., Atlan A., Bengtsson B.O. Genetic conflicts. The Quarterly Review of Biology. 71:1996;317-364.
43. Hurst L.D., McVean G.T. Growth effects of uniparental disomies and the conflict theory of genomic imprinting. Trends in Genetics. 13:1997;436-443.
44. Isles A.R., Wilkinson L.S. Imprinted genes, cognition and behavior. Trends in Cognitive Sciences. 4:2000;309-318.
45. Iwasa Y. The conflict theory of genomic imprinting: how much can be explained? Current Topics in Developmental Biology. 40:1998;255-293.
46. Jiang Y., Tsai T.-F., Bressler J., Beaudet A.L. Imprinting in Angelman and Prader-Willi Syndromes. Current Opinion in Genetics and Development. 8:1998;334-342.
47. Kandel E.R., Schwartz J.H., Jessell T.M. Essentials of neural science and behavior. 1995;Appleton and Lange, Norwalk, CT.
48. Keverne E.B. Molecular genetic approaches to understanding brain development and behavior. Psychoneuroendocrinology. 19:1994;407-414.
49. Keverne E.B. Genomic imprinting in the brain. Current Opinion in Neurobiology. 7:1997;463-468.
50. Keverne E.B., Fundele R., Narasimha M., Barton S.C., Surani M.A. Genomic imprinting and the differential roles of parental genomes in brain development. Developmental Brain Research. 92:1996;91-100.
51. Kirkness E.W., Durcan M.J. Genomic imprinting: parental origin effects on gene expression. Alcohol Health and Research World. 16:1992;312-316.
52. Lalande M., Minassian B.A., DeLorey T.M., Olsen R.W. Parental imprinting and Angelman Syndrome. Advances in Neurology. 79:1999;421-429.
53. Lefebvre L., Viville S., Barton S.C., Ishino F., Keverne E.B., Surani M.A. Abnormal maternal behavior and growth retardation associated with loss of the imprinted gene Mest. Nature Genetics. 20:1998;163-169.
54. Li L.-L., Keverne E.B., Aparicio S.A., Barton S.C., Surani M.A., Ishino F. Peg3 and the conflict hypothesis. Science. 287:2000;1167a.
55. Li L.-L., Keverne E.B., Aparicio S.A., Ishino F., Barton S.C., Surani M.A. Regulation of maternal behavior and offspring growth by paternally expressed Peg3. Science. 284:1999;330-333.
56. Lichter D.G., Jackson L.A., Schachter M. Clinical evidence of genomic imprinting in Tourette's Syndrome. Neurology. 45:1995;924-928.
57. Lindor N.M., Ney J.A., Gaffey T.A., Jenkins R.B., Thibodeau S.N., Dewald G.W. A genetic review of complete and partial hydatidiform moles and nonmolar triploidy. Mayo Clinic Proceedings. 67:1992;791-799.
58. Mann J.R., Gadi I., Harbison M.L., Abbondanzo S.J., Stewart C.L. Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting. Cell. 62:1990;251-260.
59. McFadden D.E., Kalousek D.K. Two different phenotypes of fetuses with chromosomal triploidy: correlation with parental origin of the extra haploid set. American Journal of Medical Genetics. 38:1991;535-538.
60. McGrath J., Solter D. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell. 37:1984;179-183.
61. McMahon F.J., Stinc O.C., Meyers D.A., Simpson S.G., DePaulo J.R. Patterns of maternal transmission in bipolar affective disorder. American Journal of Human Genetics. 56:1995;1277-1286.
62. A receptor subunit genes, using microcell-mediated chromosome transfer. Human Molecular Genetics. 6:1997;2127-2133.
63. Moore T., Haig D. Genomic imprinting in mammalian development: a parental tug-of-war. Trends in Genetics. 7:1991;45-49.
64. Moore T., Mills W. Imprinting and monogamy. Nature Genetics. 22:1999;130-131.
65. Morison I.M., Reeve A.E. A catalogue of imprinted genes and parent-of-origin effects in humans and animals. Human Molecular Genetics. 7:1998;1599-1609.
66. Nicholls R.D., Saitoh S., Horsthemke B. Imprinting in Prader-Willi and Angelman Syndromes. Trends in Genetics. 14:1998;194-200.
67. Nicolson N.A. Infants, mothers, and other females. Smuts B.B., Cheney D.L., Seyfarth R.M., Wrangham R.W., Struhsaker T.T. Primate societies. 1987;330-342 University of Chicago Press, Chicago.
68. Ottman R., Annegers J.F., Hauser W.A., Kurland L.T. Higher risk of seizures in offspring of mothers than of fathers with epilepsy. American Journal of Human Genetics. 43:1988;257-264.
69. Paldi A., Nagy A., Markkula M., Barna I., Dezso L. Postnatal development of parthenogenetic↔fertilized mouse aggregation chimeras. Development. 105:1989;115-118.
70. Parkinson W.L., Weingarten H.P. Dissociative analysis of ventromedial hypothalamic obesity syndrome. American Journal of Physiology. 259:1990;R829-R835.
71. Reik W. Genomic imprinting and genetic disorders in man. Trends in Genetics. 5:1989;331-336.
72. Schroer R.J., Phelan M.C., Michaelis R.C., Crawford E.C., Skinner S.A., Cuccaro M., Simensen R.J., Bishop J., Skinner C., Fender D., Stevenson R.E. Autism and maternally derived aberrations of chromosome 15q. American Journal of Medical Genetics. 76:1998;327-336.
73. Scourfield J., McGuffin P., Thapar A. Genes and social skills. BioEssays. 19:1997;1125-1127.
74. Skuse D.H., James R.S., Bishop D.V.M., Coppin B., Dalton P., Aamodt-Leeper G., Bacarese-Hamilton M., Creswell C., McGurk R., Jacobs P.A. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature. 387:1997;705-708.
75. Smits G., Parma J., Vassart G. Peg3 and the conflict hypothesis. Science. 287:2000;1167a.
76. Solter D. Differential imprinting and expression of maternal and paternal genomes. Annual Review of Genetics. 22:1988;127-146.
77. Spencer H.G., Clark A.G., Feldman M.W. Genetic conflicts and the evolutionary origin of genomic imprinting. Trends in Ecology and Evolution. 14:1999;197-201.
78. Strachan T., Read A.P. Human molecular genetics. 1996;Wiley, Rexdale, Ontario.
79. 2C serotonin receptors. Nature. 374:1995;542-546.
80. Thomson J.A., Solter D. The developmental fate of androgenetic, parthenogenetic, and gynogenetic cells in chimeric gastrulating mouse embryos. Genes and Development. 2:1988;1344-1351.
81. Trivers R. Parent-offspring conflict. American Zoologist. 14:1974;249-264.
82. Trivers R.L. Genetic basis of intrapsychic conflict. Segal N.L., Weisfeld G.E., Weisfeld C.C. Uniting psychology and biology: integrative perspectives on human development. 1997;385-395 American Psychological Association, Washington, DC.
83. Tycko B. Genomic imprinting: mechanism and role in human pathology. American Journal of Pathology. 144:1994;431-443.
84. Vrana P.B., Fossella J.A., Matteson P., del Rio T., O'Neill M.J., Tilghman S.M. Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus. Nature Genetics. 25:2000;120-124.
85. Vrana P.B., Guan X.-J., Ingram R.S., Tilghman S.M. Genomic imprinting is disrupted in interspecific Peromyscus hybrids. Nature Genetics. 20:1998;362-365.
86. A receptor β3 subunit to the Angelman/Prader-Willi region of human chromosome 15. American Journal of Human Genetics. 49:1991;330-337.
87. Wozniak D.F., Cicero T.J., Kettinger L. III, Meyer E.R. Paternal alcohol consumption in the rat impairs spatial learning performance in male offspring. Psychopharmacology. 105:1991;289-302.
88. Yamamoto Y., Huibregtse J.M., Howley P.M. The human E6-AP gene (UBE3A) encodes three potential protein isoforms generated by differential splicing. Genomics. 41:1997;263-266.
89. Yen W.M. Sex-linked major gene influences on selected types of spatial performance. Behavior Genetics. 5:1975;281-298.