4.7 Article

Protein Kinase A phosphorylates NCoR to enhance its nuclear translocation and repressive function in human prostate cancer cells

期刊

JOURNAL OF CELLULAR PHYSIOLOGY
卷 228, 期 6, 页码 1159-1165

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WILEY-BLACKWELL
DOI: 10.1002/jcp.24269

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资金

  1. National Research Foundation of Korea (NRF)
  2. ministry of education, science and technology (MEST), Korea government [2011-0011416]
  3. Asan Institute for Life Sciences, Seoul, Korea [2012-530]
  4. National Research Foundation of Korea (NRF), Ministry of Education, Science and Technology (MEST), Korea Government, Korea [2011-0011416]
  5. National Research Foundation of Korea [2011-0011416] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Protein Kinase A (PKA) phosphorylates diverse protein substrates to modulate their function. In this study, we found that PKA specifically phosphorylates the RD1 (Repression Domain 1) domain of nuclear receptor corepressor (NCoR). We demonstrated that the Serine-70 of NCoR is identified the critical amino acid for PKA-dependent NCoR phosphorylation. Importantly, we found that PKA-dependent phosphorylation enhances the nuclear translocation of NCoR. More importantly, the activation of PKA enhanced the repressive activity of NCoR in a reporter assay and potentiated the antagonist activity in the Androgen Receptor (AR)-mediated transcription. Taken together, these results uncover a regulatory mechanism by which PKA positively modulates NCoR function in transcriptional regulation in prostate cancer. J. Cell. Physiol. 228: 11591165, 2013. (c) 2012 Wiley Periodicals, Inc.

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