Charlier Thierry D, Lakaye Bernard, Ball Gregory F, Balthazart Jacques
University of Liège, Center for Cellular and Molecular Neurobiology, Research Group in Behavioral Neuroendocrinology, and Laboratory of Neurochemistry, Liège, Belgium.
Neuroendocrinology. 2002 Nov;76(5):297-315. doi: 10.1159/000066624.
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 3,411-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.
类固醇受体辅激活因子SRC-1可调节几种核受体的配体依赖性反式激活,包括性类固醇激素受体。通过注射特异性反义寡核苷酸降低SRC-1的表达,可显著抑制雌激素对大鼠脑性分化和行为的影响,并抑制成年雌性大鼠的雌性性行为激活。因此,SRC-1似乎参与了性行为的发育和激活。在日本鹌鹑脑中,我们通过RT-PCR扩增了一个3411 bp的片段,该片段从该蛋白的HLH结构域延伸至激活结构域2。鹌鹑SRC-1与哺乳动物(m)SRC-1密切相关,且含有高比例的GC核苷酸(62.5%)。其氨基酸序列与哺乳动物SRC-1的一致性为70%,并含有与核受体相互作用的三个保守LXXLL基序。在雄性和雌性中,RT-PCR显示端脑、间脑、视叶、脑干、脊髓、垂体、肝脏、肾脏、肾上腺、心脏、肺、性腺和生殖管道中的表达水平相似。雄性视前区-下丘脑的SRC-1表达水平显著高于雌性。在两性中,小脑和肌肉中的表达水平较低。利用四种地高辛标记寡核苷酸混合物进行的原位杂交在细胞水平上证实了SRC-1 mRNA在脑中的广泛分布以及在对雄性性行为控制起关键作用类固醇敏感区域的特别密集表达。这些数据证实了SRC-1的存在,并首次描述了其在鸟类脑中的分布。它们证实了其在包括脑在内的整个身体中的广泛、几乎无处不在的分布情况,这对于调节许多核受体作用的辅激活因子来说是可以预期的。然而,这种分布在脑中是异质的,并且在至少一些区域存在性别差异。SRC-1在与雄性性行为控制相关的边缘和中脑核中的非常密集的表达与该辅激活因子在这种行为激活中起重要作用的观点一致。