What does the "four core genotypes" mouse model tell us about sex differences in the brain and other tissues?

被引:395
作者
Arnold, Arthur P. [1 ]
Chen, Xuqi [1 ]
机构
[1] Univ Calif Los Angeles, Brain Res Inst, Neuroendocrinol Lab, Dept Physiol Sci, Los Angeles, CA 90095 USA
关键词
Sex chromosome; X chromosome; Y chromosome; Sex differences; Sexual differentiation; Nociception; Neural tube closure; Autoimmune disease; Addiction; COMPLEMENT AFFECTS NOCICEPTION; FEMALE EMBRYONIC LETHALITY; CHROMOSOME COMPLEMENT; NEURAL-TUBE; GENE-EXPRESSION; CANDIDATE GENE; Y-CHROMOSOME; MICE; DIFFERENTIATION; ADULT;
D O I
10.1016/j.yfrne.2008.11.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The "four core genotypes" (FCG) model comprises mice in which sex chromosome complement (XX vs. XY) is unrelated to the animal's gonadal sex. The four genotypes are XX gonadal males or females, and XY gonadal males or females. The model allows one to measure (1) the differences in phenotypes caused by sex chromosome complement (XX vs. XY), (2) the differential effects of ovarian and testicular secretions, and (3) the interactive effects of (1) and (2). Thus, the FCG model provides new information regarding the origins of sex differences in phenotype that has not been available from studies that manipulate gonadal hormone levels in normal XY males and XX females. Studies of the FCG model have uncovered XX vs. XY differences in behaviors (aggression, parenting, habit formation, nociception, social interactions), gene expression (septal vasopressin), and susceptibility to disease (neural tube closure and autoimmune disease) not mediated by gonadal hormones. Some sex chromosome effects are mediated by sex differences in dose of X genes or their parental imprint. Future studies will identify the genes involved and their mechanisms of action. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 84 条
  • [1] Neural, not gonadal, origin of brain sex differences in a gynandromorphic finch
    Agate, RJ
    Grisham, W
    Wade, J
    Mann, S
    Wingfield, J
    Schanen, C
    Palotie, A
    Arnold, AP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (08) : 4873 - 4878
  • [2] HIGH-FREQUENCY DEVELOPMENTAL ABNORMALITIES IN P53-DEFICIENT MICE
    ARMSTRONG, JF
    KAUFMAN, MH
    HARRISON, DJ
    CLARKE, AR
    [J]. CURRENT BIOLOGY, 1995, 5 (08) : 931 - 936
  • [3] Arnold A.P., 2002, Hormones, brain, and behavior, P105
  • [4] Arnold AP, 1997, J NEUROBIOL, V33, P572, DOI 10.1002/(SICI)1097-4695(19971105)33:5<572::AID-NEU6>3.3.CO
  • [5] 2-6
  • [6] GONADAL-STEROID INDUCTION OF STRUCTURAL SEX-DIFFERENCES IN THE CENTRAL NERVOUS-SYSTEM
    ARNOLD, AP
    GORSKI, RA
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 1984, 7 : 413 - 442
  • [7] Genetically triggered sexual differentiation of brain and behavior
    Arnold, AP
    [J]. HORMONES AND BEHAVIOR, 1996, 30 (04) : 495 - 505
  • [8] Sex chromosomes and brain gender
    Arnold, AP
    [J]. NATURE REVIEWS NEUROSCIENCE, 2004, 5 (09) : 701 - 708
  • [9] Are XX and XY brain cells intrinsically different?
    Arnold, AP
    Burgoyne, PS
    [J]. TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2004, 15 (01) : 6 - 11
  • [10] Two perspectives on the origin of sex differences in the brain
    Arnold, AP
    Rissman, EF
    De Vries, GJ
    [J]. STEROIDS AND THE NERVOUS SYSTEM, 2003, 1007 : 176 - 188