Hu Zhiying, Dandekar Dineshkumar, O'Shaughnessy Peter J, De Gendt Karel, Verhoeven Guido, Wilkinson Miles F
Department of Biochemistry & Molecular Biology, University of Texas M D Anderson Cancer Center, Houston, Texas 77030, USA.
Mol Endocrinol. 2010 Jan;24(1):60-75. doi: 10.1210/me.2009-0303. Epub 2009 Nov 9.
Rhox5, the founding member of the reproductive homeobox on the X chromosome (Rhox) gene cluster, encodes a homeodomain-containing transcription factor that is selectively expressed in Sertoli cells, where it promotes the survival of male germ cells. To identify Rhox5-regulated genes, we generated 15P-1 Sertoli cell clones expressing physiological levels of Rhox5 from a stably transfected expression vector. Microarray analysis identified many genes altered in expression in response to Rhox5, including those encoding proteins controlling cell cycle regulation, apoptosis, metabolism, and cell-cell interactions. Fifteen of these Rhox5-regulated genes were chosen for further analysis. Analysis of Rhox5-null male mice indicated that at least nine of these are Rhox5-regulated in the testes in vivo. Many of them have distinct postnatal expression patterns and are regulated by Rhox5 at different postnatal time points. Most of them are expressed in Sertoli cells, indicating that they are candidates to be directly regulated by Rhox5. Transfection analysis with expression vectors encoding different mouse and human Rhox family members revealed that the regulatory response of a subset of these Rhox5-regulated genes is both conserved and redundant. Given that Rhox5 depends on androgen receptor (AR) for expression in Sertoli cells, we examined whether some Rhox5-regulated genes are also regulated by AR. We provide several lines of evidence that this is the case, leading us to propose that RHOX5 serves as a key intermediate transcription factor that directs some of the actions of AR in the testes.
Rhox5是X染色体上生殖同源框(Rhox)基因簇的首个成员,编码一种含同源结构域的转录因子,该因子在支持细胞中选择性表达,可促进雄性生殖细胞的存活。为了鉴定受Rhox5调控的基因,我们从稳定转染的表达载体中生成了表达生理水平Rhox5的15P - 1支持细胞克隆。微阵列分析确定了许多因Rhox5而表达发生改变的基因,包括那些编码控制细胞周期调控、细胞凋亡、代谢及细胞间相互作用的蛋白质的基因。从这些受Rhox5调控的基因中挑选了15个进行进一步分析。对Rhox5基因敲除雄性小鼠的分析表明,其中至少有9个基因在体内睾丸中受Rhox5调控。它们中的许多具有独特的出生后表达模式,并在不同的出生后时间点受Rhox5调控。它们中的大多数在支持细胞中表达,表明它们可能是受Rhox5直接调控的候选基因。用编码不同小鼠和人类Rhox家族成员的表达载体进行转染分析表明,这些受Rhox5调控的基因中有一部分的调控反应具有保守性和冗余性。鉴于Rhox5在支持细胞中的表达依赖雄激素受体(AR),我们研究了一些受Rhox5调控的基因是否也受AR调控。我们提供了几条证据表明情况确实如此,这使我们提出RHOX5作为一个关键的中间转录因子,指导AR在睾丸中的一些作用。