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Transcription ; 10(3): 147-156, 2019 06.
Article in English | MEDLINE | ID: mdl-31135261

ABSTRACT

Transcriptional activation by PML-RARα, an acute promyelocytic leukemia-related oncofusion protein, requires pharmacological concentrations of all-trans retinoic acid (ATRA). However, the mechanism by which the liganded PML-RARα complex leads to the formation of the preinitiation complex has been unidentified. Here we demonstrate that the Mediator subunit MED1 plays an important role in the ATRA-dependent activation of the PML-RARα-bound promoter. Luciferase reporter assays showed that PML-RARα induced significant transcription at pharmacological doses (1 µM) of ATRA; however, this was submaximal and equivalent to the level of transcription driven by intact RARα at physiological doses (1 nM) of ATRA. Transcription depended upon the interaction of PML-RARα with the two LxxLL nuclear receptor recognition motifs of MED1, and LxxLL→LxxAA mutations led to minimal transcription. Mechanistically, MED1 interacted ATRA-dependently with the RARα portion of PML-RARα through the two LxxLL motifs of MED1. These results suggest that PML-RARα initiates ATRA-induced transcription through its interaction with MED1.


Subject(s)
Mediator Complex Subunit 1/metabolism , Oncogene Proteins, Fusion/agonists , Oncogene Proteins, Fusion/metabolism , Transcriptional Activation/drug effects , Tretinoin/pharmacology , Humans , Mediator Complex Subunit 1/chemistry , Protein Binding/drug effects
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