TY - JOUR
T1 - Gender-Specific Gene Expression in Post-Mortem Human Brain
T2 - Localization to Sex Chromosomes
AU - Vawter, Marquis P.
AU - Evans, Simon
AU - Choudary, Prabhakara
AU - Tomita, Hiroaki
AU - Meador-Woodruff, Jim
AU - Molnar, Margherita
AU - Li, Jun
AU - Lopez, Juan F.
AU - Myers, Rick
AU - Cox, David
AU - Watson, Stanley J.
AU - Akil, Huda
AU - Jones, Edward G.
AU - Bunney, William E.
N1 - Funding Information:
We appreciate the assistance of Richard Stein, PhD, David Walsh, PsyD, and Preston Cartagena, PsyD for their contributions to post-mortem clinical characterization of subjects and Kathleen Burke for procurement of brain tissue, as well as Jacque Berndt and the investigators and medical examiners at the Orange County Coroners Office. We also appreciate the technical contributions of Erick Ferran, Karen Lopez, Sharon Burke, and Phong Nguyen. F Warren Lovell, MD, performed a neuropathological evaluation of the post-mortem brains. Tissue specimens were processed and stored at the Human Brain and Spinal Fluid Resource Center, Veterans Medical Center, Los Angeles under the direction of Wallace W Tourtellotte, MD, PhD. This project is supported by the NIMH Conte Center Grant P50 MH60398, Pritzker Neuropsychiatric Disorders Research Consortium, William Lion Penzner Foundation (UCI), Della Martin Foundation (UCI), NIMH Grant #MH54844 (EGJ), WM Keck Foundation (EGJ), and the NIMH Program Project MH42251 (SJW and HA).
PY - 2004/2
Y1 - 2004/2
N2 - Gender differences in brain development and in the prevalence of neuropsychiatric disorders such as depression have been reported. Gender differences in human brain might be related to patterns of gene expression. Microarray technology is one useful method for investigation of gene expression in brain. We investigated gene expression, cell types, and regional expression patterns of differentially expressed sex chromosome genes in brain. We profiled gene expression in male and female dorsolateral prefrontal cortex, anterior cingulate cortex, and cerebellum using the Affymetrix oligonudeotide microarray platform. Differentially expressed genes between males and females on the Y chromosome (DBY, SMCY, UTY, RPS4Y, and USP9Y) and X chromosome (XIST) were confirmed using real-time PCR measurements. In situ hybridization confirmed the differential expression of gender-specific genes and neuronal expression of XIST, RPS4Y, SMCY, and UTY in three brain regions examined. The XIST gene, which silences gene expression on regions of the X chromosome, is expressed in a subset of neurons. Since a subset of neurons express gender-specific genes, neural subpopulations may exhibit a subtle sexual dimorphism at the level of differences in gene regulation and function. The distinctive pattern of neuronal expression of XIST, RPS4Y, SMCY, and UTY and other sex chromosome genes in neuronal subpopulations may possibly contribute to gender differences in prevalence noted for some neuropsychiatric disorders. Studies of the protein expression of these sex-chromosome-linked genes in brain tissue are required to address the functional consequences of the observed gene expression differences.
AB - Gender differences in brain development and in the prevalence of neuropsychiatric disorders such as depression have been reported. Gender differences in human brain might be related to patterns of gene expression. Microarray technology is one useful method for investigation of gene expression in brain. We investigated gene expression, cell types, and regional expression patterns of differentially expressed sex chromosome genes in brain. We profiled gene expression in male and female dorsolateral prefrontal cortex, anterior cingulate cortex, and cerebellum using the Affymetrix oligonudeotide microarray platform. Differentially expressed genes between males and females on the Y chromosome (DBY, SMCY, UTY, RPS4Y, and USP9Y) and X chromosome (XIST) were confirmed using real-time PCR measurements. In situ hybridization confirmed the differential expression of gender-specific genes and neuronal expression of XIST, RPS4Y, SMCY, and UTY in three brain regions examined. The XIST gene, which silences gene expression on regions of the X chromosome, is expressed in a subset of neurons. Since a subset of neurons express gender-specific genes, neural subpopulations may exhibit a subtle sexual dimorphism at the level of differences in gene regulation and function. The distinctive pattern of neuronal expression of XIST, RPS4Y, SMCY, and UTY and other sex chromosome genes in neuronal subpopulations may possibly contribute to gender differences in prevalence noted for some neuropsychiatric disorders. Studies of the protein expression of these sex-chromosome-linked genes in brain tissue are required to address the functional consequences of the observed gene expression differences.
KW - DBY
KW - RPS4Y
KW - SMCY
KW - USP9Y
KW - UTY
KW - VCX
KW - VCY
KW - XIST
UR - http://www.scopus.com/inward/record.url?scp=10744226630&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=10744226630&partnerID=8YFLogxK
U2 - 10.1038/sj.npp.1300337
DO - 10.1038/sj.npp.1300337
M3 - Article
C2 - 14583743
AN - SCOPUS:10744226630
SN - 0893-133X
VL - 29
SP - 373
EP - 384
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 2
ER -