Core promoter-selective function of HMGA1 and Mediator in Initiator-dependent transcription
- 1Department of Biochemistry,
- 2W.M. Keck Proteomics Laboratory of the Institute for Integrative Genome Biology, University of California at Riverside, Riverside, California 92521, USA;
- 3Laboratory of Biochemistry and Molecular Biology, The Rockefeller University, New York, New York 10065, USA
Abstract
The factors and mechanisms underlying the differential activity and regulation of eukaryotic RNA polymerase II on different types of core promoters have remained elusive. Here we show that the architectural factor HMGA1 and the Mediator coregulator complex cooperate to enhance basal transcription from core promoters containing both a TATA box and an Initiator (INR) element but not from “TATA-only” core promoters. INR-dependent activation by HMGA1 and Mediator requires the TATA-binding protein (TBP)-associated factors (TAFs) within the TFIID complex and counteracts negative regulators of TBP/TATA-dependent transcription such as NC2 and Topoisomerase I. HMGA1 interacts with TFIID and Mediator and is required for the synergy of TATA and INR elements in mammalian cells. Accordingly, natural HMGA1-activated genes in embryonic stem cells tend to have both TATA and INR elements in a synergistic configuration. Our results suggest a core promoter-specific regulation of Mediator and the basal transcription machinery by HMGA1.
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Footnotes
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↵4 Corresponding author.
E-mail ernest.martinez{at}ucr.edu.
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Supplemental material is available for this article.
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Article is online at http://www.genesdev.org/cgi/doi/10.1101/gad.177360.111.
- Received August 18, 2011.
- Accepted October 26, 2011.
- Copyright © 2011 by Cold Spring Harbor Laboratory Press










