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Molecular and Cellular Biology, February 2009, p. 613-625, Vol. 29, No. 3
0270-7306/09/$08.00+0     doi:10.1128/MCB.00295-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

SUMOylation Inhibits SF-1 Activity by Reducing CDK7-Mediated Serine 203 Phosphorylation{triangledown}

Wei-Hsiung Yang,1,3 Joanne H. Heaton,1 Holly Brevig,2 Sarmistha Mukherjee,2 Jorge A. Iñiguez-Lluhí,2 and Gary D. Hammer1*

Department of Internal Medicine, Division of Metabolism, Endocrinology, and Diabetes,1 Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan,2 Department of Biomedical Sciences, Mercer University School of Medicine, Savannah, Georgia3

Received 21 February 2008/ Returned for modification 25 March 2008/ Accepted 31 October 2008

Steroidogenic factor 1 (SF-1) is an orphan nuclear receptor selectively expressed in the adrenal cortex and gonads, where it mediates the hormonal stimulation of multiple genes involved in steroid hormone biosynthesis. SF-1 is the target of both phosphorylation and SUMOylation, but how these modifications interact or contribute to SF-1 regulation of endogenous genes remains poorly defined. We found that SF-1 is selectively SUMOylated at K194 in Y1 adrenocarcinoma cells and that although SUMOylation does not alter the subcellular localization of SF-1, the modification inhibits the ability of SF-1 to activate target genes. Notably, whereas SF-1 SUMOylation is independent of S203 phosphorylation and is unaffected by adrenocorticotropin (ACTH) treatment, loss of SUMOylation leads to enhanced SF-1 phosphorylation at serine 203. Furthermore, preventing SF-1 SUMOylation increases the mRNA and protein levels of multiple steroidogenic enzyme genes. Analysis of the StAR promoter indicates that blockade of SF-1 SUMOylation leads to an increase in overall promoter occupancy but does not alter the oscillatory recruitment dynamics in response to ACTH. Notably, we find that CDK7 binds preferentially to the SUMOylation-deficient form of SF-1 and that CDK7 inhibition reduces phosphorylation of SF-1. Based on these observations, we propose a coordinated modification model in which inhibition of SF-1-mediated transcription by SUMOylation in adrenocortical cancer cells is mediated through reduced CDK7-induced phosphorylation of SF-1.

*Corresponding author. Present address: BSRB 1502, 109 Zina Pitcher Place, University of Michigan, Ann Arbor, MI 48109-2200. Phone: (734) 615-2421. Fax: (734) 615-4356. E-mail: ghammer{at}umich.edu

{triangledown} Published ahead of print on 17 November 2008.

Molecular and Cellular Biology, February 2009, p. 613-625, Vol. 29, No. 3
0270-7306/09/$08.00+0     doi:10.1128/MCB.00295-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Ogawa, H., Komatsu, T., Hiraoka, Y., Morohashi, K.-i. (2009). Transcriptional Suppression by Transient Recruitment of ARIP4 to Sumoylated Nuclear Receptor Ad4BP/SF-1. Mol. Biol. Cell 20: 4235-4245 [Abstract] [Full Text]  
  • Kim, A. C., Barlaskar, F. M., Heaton, J. H., Else, T., Kelly, V. R., Krill, K. T., Scheys, J. O., Simon, D. P., Trovato, A., Yang, W.-H., Hammer, G. D. (2009). In Search of Adrenocortical Stem and Progenitor Cells. Endocr. Rev. 30: 241-263 [Abstract] [Full Text]  
  • Xu, B., Yang, W.-H., Gerin, I., Hu, C.-D., Hammer, G. D., Koenig, R. J. (2009). Dax-1 and Steroid Receptor RNA Activator (SRA) Function as Transcriptional Coactivators for Steroidogenic Factor 1 in Steroidogenesis. Mol. Cell. Biol. 29: 1719-1734 [Abstract] [Full Text]  


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