Modulation of testicular receptor 4 activity by mitogen-activated protein kinase-mediated phosphorylation

M. D Mostaqul Huq, Pawan Gupta, Nien Pei Tsai, Li-Na Wei

Research output: Contribution to journalArticlepeer-review

27 Scopus citations


Testicular receptor 4 (TR4) is an orphan member of the nuclear receptor superfamily. Despite the lack of identified ligands, its functional role has been demonstrated both in animals and cell cultures. However, it remains unclear how the biological activity of TR4 is regulated without specific ligands. In this study, we showed that in the absence of specific ligands the activity of TR4 could be modulated by mitogen-activated protein kinase (MAPK)-mediated phosphorylation of its activation function 1 (AF-1) domain. A mass spectrometry-based proteome analysis of TR4 expressed in insect cells revealed three phosphorylation sites in its AF-1 domain, specifically on Ser19, Sera55, and Sere68. Site-directed mutagenesis studies demonstrated the functionality of phosphorylation on Ser19 and Sere68 but not Ser55. We also demonstrated that MAPK-mediated phosphorylation of the AF-1 domain rendered TR4 a repressor, mediated through the preferential recruitment of corepressor RIP140. Dephosphorylation of its AF-1 made TR4 an activator due to its selective recruitment of coactivator, P300/ cyclic AMP-responsive element binding protein-binding protein-associated factor (PCAF). The biological effects were validated by using the wild type TR4 and its constitutive negative (dephosphorylated) and constitutive positive (phosphorylated) mutants in the studies of regulation of its natural target gene, apoE. This study uncovered, for the first time, a ligand-independent mechanism underlying the biological activity of TR4 that was mediated by MAPK-mediated receptor phosphorylation of AF-1 domain.

Original languageEnglish (US)
Pages (from-to)2072-2082
Number of pages11
JournalMolecular and Cellular Proteomics
Issue number11
StatePublished - Nov 2006


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