4.7 Review

The Mediator complex as a master regulator of transcription by RNA polymerase II

Journal

NATURE REVIEWS MOLECULAR CELL BIOLOGY
Volume 23, Issue 11, Pages 732-749

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41580-022-00498-3

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Funding

  1. NIH [R35 GM139550]
  2. NSF [MCB-190330, MCB-1818147]

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The Mediator complex is a crucial regulator of RNA polymerase II. This Review focuses on recent structural insights into Mediator function and proposes a model that addresses conflicting data regarding whether enhancer-promoter communication during transcription is direct or indirect.
The Mediator complex, which in humans is 1.4 MDa in size and includes 26 subunits, controls many aspects of RNA polymerase II (Pol II) function. Apart from its size, a defining feature of Mediator is its intrinsic disorder and conformational flexibility, which contributes to its ability to undergo phase separation and to interact with a myriad of regulatory factors. In this Review, we discuss Mediator structure and function, with emphasis on recent cryogenic electron microscopy data of the 4.0-MDa transcription preinitiation complex. We further discuss how Mediator and sequence-specific DNA-binding transcription factors enable enhancer-dependent regulation of Pol II function at distal gene promoters, through the formation of molecular condensates (or transcription hubs) and chromatin loops. Mediator regulation of Pol II reinitiation is also discussed, in the context of transcription bursting. We propose a working model for Mediator function that combines experimental results and theoretical considerations related to enhancer-promoter interactions, which reconciles contradictory data regarding whether enhancer-promoter communication is direct or indirect. We conclude with a discussion of Mediator's potential as a therapeutic target and of future research directions. The Mediator complex is an important regulator of RNA polymerase II. This Review discusses recent structural insights into Mediator function and proposes a model that reconciles contradictory data on whether enhancer-promoter communication during transcription is direct or indirect.

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