Mediator and RNA polymerase II clusters associate in transcription-dependent condensates

Author:

Cho Won-Ki1ORCID,Spille Jan-Hendrik1ORCID,Hecht Micca1ORCID,Lee Choongman1,Li Charles23ORCID,Grube Valentin14,Cisse Ibrahim I.1ORCID

Affiliation:

1. Department of Physics, MIT, Cambridge, MA 02139, USA.

2. Department of Biology, MIT, Cambridge, MA 02139, USA.

3. Whitehead Institute for Biomedical Research, Cambridge, MA 02139, USA.

4. Department of Physics, LMU Munich, Geschwister Scholl Platz 1, 80539 Munich, Germany.

Abstract

Phase separation and gene control Many components of eukaryotic transcription machinery—such as transcription factors and cofactors including BRD4, subunits of the Mediator complex, and RNA polymerase II—contain intrinsically disordered low-complexity domains. Now a conceptual framework connecting the nature and behavior of their interactions to their functions in transcription regulation is emerging (see the Perspective by Plys and Kingston). Chong et al. found that low-complexity domains of transcription factors form concentrated hubs via functionally relevant dynamic, multivalent, and sequence-specific protein-protein interaction. These hubs have the potential to phase-separate at higher concentrations. Indeed, Sabari et al. showed that at super-enhancers, BRD4 and Mediator form liquid-like condensates that compartmentalize and concentrate the transcription apparatus to maintain expression of key cell-identity genes. Cho et al. further revealed the differential sensitivity of Mediator and RNA polymerase II condensates to selective transcription inhibitors and how their dynamic interactions might initiate transcription elongation. Science , this issue p. eaar2555 , p. eaar3958 , p. 412 ; see also p. 329

Funder

NIH Office of the Director

Pew Charitable Trusts

German Research Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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