Concordant Androgen-Regulated Expression of Divergent Rhox5 Promoters in Sertoli Cells

Author:

Bhardwaj Anjana12ORCID,Sohni Abhishek3ORCID,Lou Chih-Hong3,De Gendt Karel34,Zhang Fanmao1,Kim Eunah15,Subbarayalu Panneerdoss6ORCID,Chan Waikin1,Kerkhofs Stefanie4,Claessens Frank4ORCID,Kimmins Sarah7ORCID,Rao Manjeet K6ORCID,Meistrich Marvin8ORCID,Wilkinson Miles F39ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA

2. Department of Breast Surgical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA

3. School of Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Diego, La Jolla, CA 92093-0695, USA

4. KU Leuven, Campus Gasthuisberg, O/N1, BE-3000 Leuven, Belgium

5. Department of Environmental Health and Safety, University of Texas Health Sciences Center, Houston, TX, USA

6. Department of Cell Systems and Anatomy, University of Texas Health San Antonio, San Antonio, TX 78229, USA

7. Department of Animal Sciences, McGill University Montreal, Quebec H3A 0G4, Canada

8. Department of Experimental Radiation Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA

9. Institute of Genomic Medicine, University of California, San Diego, La Jolla, CA 92093, USA

Abstract

Abstract 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.

Funder

National Institutes of Health

Publisher

The Endocrine Society

Subject

Endocrinology

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