Bhardwaj Anjana, Sohni Abhishek, Lou Chih-Hong, De Gendt Karel, Zhang Fanmao, Kim Eunah, Subbarayalu Panneerdoss, Chan Waikin, Kerkhofs Stefanie, Claessens Frank, Kimmins Sarah, Rao Manjeet K, Meistrich Marvin, Wilkinson Miles F
Department of Biochemistry and Molecular Biology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Department of Breast Surgical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA.
Endocrinology. 2022 Jan 1;163(1). doi: 10.1210/endocr/bqab237.
Concordant transcriptional regulation can generate multiple gene products that collaborate to achieve a common goal. Here we report a case of concordant transcriptional regulation that instead drives a single protein to be produced in the same cell type from divergent promoters. This gene product-the RHOX5 homeobox transcription factor-is translated from 2 different mRNAs with different 5' untranslated regions (UTRs) transcribed from alternative promoters. Despite the fact that these 2 promoters-the proximal promoter (Pp) and the distal promoter (Pd)-exhibit different patterns of tissue-specific activity, share no obvious sequence identity, and depend on distinct transcription factors for expression, they exhibit a remarkably similar expression pattern in the testes. In particular, both depend on androgen signaling for expression in the testes, where they are specifically expressed in Sertoli cells and have a similar stage-specific expression pattern during the seminiferous epithelial cycle. We report evidence for 3 mechanisms that collaborate to drive concordant Pp/Pd expression. First, both promoters have an intrinsic ability to respond to androgen receptor and androgen. Second, the Pp acts as an enhancer to promote androgen-dependent transcription from the Pd. Third, Pd transcription is positively autoregulated by the RHOX5 protein, which is first produced developmentally from the Pp. Together, our data support a model in which the Rhox5 homeobox gene evolved multiple mechanisms to activate both of its promoters in Sertoli cells to produce Rhox5 in an androgen-dependent manner during different phases of spermatogenesis.
协同转录调控可产生多种基因产物,这些产物协同作用以实现共同目标。在此,我们报告了一例协同转录调控的情况,该调控反而促使在同一细胞类型中从不同启动子产生单一蛋白质。这种基因产物——RHOX5同源框转录因子——由从替代启动子转录而来的具有不同5'非翻译区(UTR)的两种不同mRNA翻译产生。尽管这两个启动子——近端启动子(Pp)和远端启动子(Pd)——表现出不同的组织特异性活性模式,没有明显的序列同一性,且依赖于不同的转录因子进行表达,但它们在睾丸中表现出非常相似的表达模式。特别是,二者在睾丸中的表达均依赖雄激素信号传导,它们在睾丸支持细胞中特异性表达,并且在生精上皮周期中具有相似的阶段特异性表达模式。我们报告了三种协同作用以驱动Pp/Pd协同表达的机制的证据。首先,两个启动子都具有响应雄激素受体和雄激素的内在能力。其次,Pp作为增强子促进Pd的雄激素依赖性转录。第三,Pd转录由RHOX5蛋白正向自调控,该蛋白最初在发育过程中由Pp产生。总之,我们的数据支持一种模型,即Rhox5同源框基因进化出多种机制,以在支持细胞中激活其两个启动子,从而在精子发生的不同阶段以雄激素依赖性方式产生Rhox5。