Steroid receptor coactivator SRC-1 exhibits high expression in steroid-sensitive brain areas regulating reproductive behaviors in the quail brain

被引:34
|
作者
Charlier, TD
Lakaye, B
Ball, GF
Balthazart, J
机构
[1] Univ Liege, Ctr Cellular & Mol Neurobiol, Res Grp Behav Neuroendorinol, B-4020 Liege, Belgium
[2] Neurochem Lab, Liege, Belgium
[3] Johns Hopkins Univ, Dept Psychol & Brain Sci, Baltimore, MD USA
关键词
gonadal steroids; gonadal steroid receptors; sex dimorphism; aromatase; sex behavior; preoptic nucleus; bed nucleus striae terminalis; quail; molecular neuroendocrinology;
D O I
10.1159/000066624
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The steroid receptor coactivator SRC-1 modulates ligand-dependent transactivation of several nuclear receptors, including the receptors for sex steroid hormones. Reducing the expression of SRC-1 by injection of specific antisense oligonucleotides markedly inhibits the effects of estrogens of the sexual differentiation of brain and behavior in rats and inhibits the activation of female sexual behavior in adult female rats. SRC-1 thus appears to be involved in both the development and activation of sexual behavior. In the Japanese quail brain, we amplified by RT-PCR a 3,41 1-bp fragment extending from the HLH domain to the activating domain-2 of the protein. The quail SRC-1 is closely related to the mammalian (m) SRC-1 and contains a high proportion of GC nucleotides (62.5%). Its amino acid sequence presents 70% identity with mammalian SRC-1 and contains the three conserved LXXLL boxes involved in the interaction with nuclear receptors. In both males and females, RT-PCR demonstrates a similarly high level of expression in the telencephalon, diencephalon, optic lobes, brain stem, spinal cord, pituitary, liver, kidney, adrenal gland, heart, lung, gonads and gonoducts. Males express significantly higher levels of SRC-1 in the preoptic area-hypothalamus than females. In both sexes, lower levels of expression are observed in the cerebellum and muscles. In situ hybridization utilizing a mixture of four digoxigenin-labeled oligonucleotides; confirms at the cellular level the widespread distribution of SRC-1 mRNA in the brain and a particularly dense expression in steroid-sensitive areas that play a key role in the control of male sexual behavior. These data confirm the presence and describe for the first time the SRC-1 distribution in the brain of an avian species. They confirm its broad, nearly ubiquitous, distribution in the entire body including the brain as could be expected for a coactivator that regulates to the action of many nuclear receptors. However this distribution is heterogeneous in the brain and sexually differentiated in at least some areas. The very dense expression of SRC-1 in limbic and mesencephalic nuclei that are associated with the control of male sexual behavior is consistent with the notion that this coactivator plays a significant role in the activation of this behavior. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:297 / 315
页数:19
相关论文
共 50 条
  • [31] Steroid receptor coactivator-1 (SRC-1) enhances ligand-dependent and receptor-dependent cell-free transcription of chromatin
    Liu, Z
    Wong, JM
    Tsai, SY
    Tsai, MJ
    O'Malley, BW
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (17) : 9485 - 9490
  • [32] A C619Y mutation in the human androgen receptor causes inactivation and mislocalization of the receptor with concomitant sequestration of SRC-1 (steroid receptor coactivator 1)
    Nazareth, LV
    Stenoien, DL
    Bingman, WE
    James, AJ
    Wu, C
    Zhang, YX
    Edwards, DP
    Mancini, W
    Marcelli, M
    Lamb, DJ
    Weigel, NL
    MOLECULAR ENDOCRINOLOGY, 1999, 13 (12) : 2065 - 2075
  • [33] Steroid Receptor Coactivator-1 (SRC-1) Promoted Cell Metastasis of Gastric Cancer via VEGFC Activator by NF-κB
    Zhao, Xiaojun
    You, Xiaolan
    Huang, Chuanjiang
    Liu, Guiyuan
    Cheng, Zhiyi
    Zhang, Haitao
    CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2022, 32 (04): : 21 - 29
  • [34] Alterations of steroid receptor coactivator-1 (SRC-1) immunoreactivities in specific brain regions of young and middle-aged female Sprague-Dawley rats (vol 1381, pg 88, 2011)
    Zhang, Dongmei
    Guo, Qiang
    Bian, Chen
    Zhang, Jiqiang
    Lin, Sen
    Su, Bingyin
    BRAIN RESEARCH, 2011, 1389 : 200 - 201
  • [35] Interaction of Developmental Transcription Factor HOXC11 with Steroid Receptor Coactivator SRC-1 Mediates Resistance to Endocrine Therapy in Breast Cancer
    McIlroy, Marie
    McCartan, Damian
    Early, Sarah
    Gaora, Peadar O.
    Pennington, Stephen
    Hill, Arnold D. K.
    Young, Leonie S.
    CANCER RESEARCH, 2010, 70 (04) : 1585 - 1594
  • [36] BLT1 (LTB4 receptor) Expression on Peripheral Blood T Cells of Steroid-Sensitive and Steroid-Resistant Asthmatics
    Chung, E. H.
    Jia, Y.
    Ohnishi, H.
    Collins, M.
    Takeda, K.
    Gelfand, E. W.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 125 (02) : AB188 - AB188
  • [37] Gene knock down via antisense oligonucleotides to the steroid receptor coactivator SRC-1 modulates testosterone-dependent male sexual behavior and neural gene expression.
    Charlier, TD
    Ball, GF
    Balthazart, J
    HORMONES AND BEHAVIOR, 2004, 46 (01) : 86 - 86
  • [38] Hormonal Regulation of Steroid Receptor Coactivator-1 mRNA in the Male and Female Green Anole Brain
    Kerver, H. N.
    Wade, J.
    JOURNAL OF NEUROENDOCRINOLOGY, 2015, 27 (03) : 223 - 233
  • [39] Sequential recruitment of steroid receptor coactivator-1 (SRC-1) and p300 enhances progesterone receptor-dependent initiation and reinitiation of transcription from chromatin
    Liu, Z
    Wong, JM
    Tsai, SY
    Tsai, MJ
    O'Malley, BW
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (22) : 12426 - 12431
  • [40] Nuclear receptor-binding sites of coactivators glucocorticoid receptor interacting protein 1 (GRIP1) and steroid receptor coactivator 1 (SRC-1): Multiple motifs with different binding specificities
    Ding, XF
    Anderson, CM
    Ma, H
    Hong, H
    Uht, RM
    Kushner, PJ
    Stallcup, MR
    MOLECULAR ENDOCRINOLOGY, 1998, 12 (02) : 302 - 313