The long term goal of the proposed studies is to understand the molecular signals that initiate sexually dimorphic development of the brain, and lead to sex differences in behavior. A great deal of experimental evidence indicates that one of these signals is testosterone, secreted by the testes before or after birth, which acts directly or indirectly on the brain of males to cause masculine patterns of neural development. However, some sex differences in the brain are not induced by gonadal steroids, and the proposed studies test an alternative hypothesis, that genes on the sex chromosomes are differentially expressed in male and female brain and lead, via non- hormonal mechanisms, to sex differences in neural development and behavior. To analyze this hypothesis, we will measure various parameters of brain structure and function, and of behavior, in male and female mice of selected genotypes that carry different numbers of X and Y chromosomes, or different portion of the sex chromosomes in varying numbers. The parameters to be measured are known sexual dimorphisms in brain structure and function and behavior. The proposed studies will determine if any genes on the Y or X chromosome contribute to sex differences in neural and behavioral development, and will narrow down the location of these genes to specific regions of the sex chromosomes. The proposed research will contribute significantly to an understanding of the principles of sexual differentiation of the brain. At issue are the molecular mechanisms by which male and female brains differ, which is highly relevant to biological basis of abnormalities of sexual differentiation, and to the explanation of sex differences in psychiatric and neural disease (e.g., Alzheimer's Disease and Multiple Sclerosis).

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH059268-01
Application #
2743910
Study Section
Special Emphasis Panel (ZRG1-IFCN-2 (01))
Program Officer
Kitt, Cheryl A
Project Start
1999-01-01
Project End
2001-12-31
Budget Start
1999-01-01
Budget End
1999-12-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Physiology
Type
Schools of Arts and Sciences
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Arnold, Arthur P (2012) The end of gonad-centric sex determination in mammals. Trends Genet 28:55-61
Arnold, Arthur P (2009) Mouse models for evaluating sex chromosome effects that cause sex differences in non-gonadal tissues. J Neuroendocrinol 21:377-86
Arnold, Arthur P; Chen, Xuqi (2009) What does the ""four core genotypes"" mouse model tell us about sex differences in the brain and other tissues? Front Neuroendocrinol 30:1-9
Xu, Jun; Watkins, Rebecca; Arnold, Arthur P (2006) Sexually dimorphic expression of the X-linked gene Eif2s3x mRNA but not protein in mouse brain. Gene Expr Patterns 6:146-55
Xu, Jun; Taya, Shinichiro; Kaibuchi, Kozo et al. (2005) Spatially and temporally specific expression in mouse hippocampus of Usp9x, a ubiquitin-specific protease involved in synaptic development. J Neurosci Res 80:47-55
Xu, Jun; Arnold, Arthur P (2005) Sexually dimorphic expression of co-repressor Sin3A in mouse kidneys. Endocr Res 31:111-9
Xu, J; Taya, S; Kaibuchi, K et al. (2005) Sexually dimorphic expression of Usp9x is related to sex chromosome complement in adult mouse brain. Eur J Neurosci 21:3017-22
Xu, Jun (2005) Age-related changes in Usp9x protein expression and DNA methylation in mouse brain. Brain Res Mol Brain Res 140:17-24
Wagner, Christine K; Xu, Jun; Pfau, Jennifer L et al. (2004) Neonatal mice possessing an Sry transgene show a masculinized pattern of progesterone receptor expression in the brain independent of sex chromosome status. Endocrinology 145:1046-9
Arnold, Arthur P; Xu, Jun; Grisham, William et al. (2004) Minireview: Sex chromosomes and brain sexual differentiation. Endocrinology 145:1057-62

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