Lee Yong Soo, Kim Hyun-Jin, Lee Hyun Ju, Lee Jae Woon, Chun Sang-Young, Ko Sun-Kun, Lee Keesook
Hormone Research Center, Chonnam National University, Gwangju 500-757, Republic of Korea.
Biol Reprod. 2002 Nov;67(5):1580-7. doi: 10.1095/biolreprod.102.006155.
Activating signal cointegrator 1 (ASC-1) has been recently reported as a coactivator of some nuclear receptors. In the present study, we have analyzed the expression of ASC-1 in the mouse testis and investigated its capacity to modulate the transcriptional activity of androgen receptor (AR). We found that although ASC-1 mRNA was ubiquitously expressed at a low level in mouse tissues, a couple of testis-specific mRNAs were expressed in the adult testis. Cloning of one testis-specific variant revealed that the ubiquitous and testis-specific transcripts of ASC-1 share at least the same open reading frame. The expression of the testis-specific ASC-1 mRNAs was developmentally regulated, and the onset of their expression coincided with the initiation of spermatogenesis. In situ hybridization of mouse testis with ASC-1 antisense probe demonstrated predominant expression of ASC-1 in the interstitial Leydig cells that express AR. Moreover, yeast two-hybrid tests and glutathione S-transferase pull-down assays revealed that ASC-1 associates directly with AR and that the hinge domain of AR and a putative zinc-finger motif of ASC-1 are major determinants for their interaction. Transient transfection assays performed by expressing ASC-1 in combination with AR and an androgen-responsive reporter gene showed that ASC-1 moderately alters the induction of the reporter gene. Taken together, these results suggest that ASC-1 may function as an AR coregulator and have a role in testicular functions.
激活信号共整合因子1(ASC-1)最近被报道为一些核受体的共激活因子。在本研究中,我们分析了ASC-1在小鼠睾丸中的表达,并研究了其调节雄激素受体(AR)转录活性的能力。我们发现,尽管ASC-1 mRNA在小鼠组织中普遍低水平表达,但在成年睾丸中表达了一些睾丸特异性mRNA。对一种睾丸特异性变体的克隆显示,ASC-1的普遍存在和睾丸特异性转录本至少共享相同的开放阅读框。睾丸特异性ASC-1 mRNA的表达受发育调控,其表达的开始与精子发生的起始相一致。用ASC-1反义探针对小鼠睾丸进行原位杂交显示,ASC-1在表达AR的间质Leydig细胞中主要表达。此外,酵母双杂交试验和谷胱甘肽S-转移酶下拉试验表明,ASC-1直接与AR结合,AR的铰链区和ASC-1的一个假定锌指基序是它们相互作用的主要决定因素。通过将ASC-1与AR和雄激素反应性报告基因一起表达进行的瞬时转染试验表明,ASC-1适度改变报告基因的诱导。综上所述,这些结果表明ASC-1可能作为AR的共调节因子,并在睾丸功能中发挥作用。