Faculty, Staff and Student Publications

Language

English

Publication Date

10-1-2024

Journal

Current Opinion in Structural Biology

DOI

10.1016/j.sbi.2024.102892

PMID

39067114

PMCID

PMC11779508

PubMedCentral® Posted Date

10-1-2025

PubMedCentral® Full Text Version

Author MSS

Abstract

The eukaryotic Mediator, comprising a large Core (cMED) and a dissociable CDK8 kinase module (CKM), functions as a critical coregulator during RNA polymerase II (RNAPII) transcription. cMED recruits RNAPII and facilitates the assembly of the pre-initiation complex (PIC) at promoters. In contrast, CKM prevents RNAPII binding to cMED while simultaneously exerting positive or negative influence on gene transcription through its kinase function. Recent structural studies on cMED and CKM have revealed their intricate architectures and subunit interactions. Here, we explore these structures, providing a comprehensive insight into Mediator (cMED-CKM) architecture and its potential mechanism in regulating RNAPII transcription. Additionally, we discuss the remaining puzzles that require further investigation to fully understand how cMED coordinates with CKM to regulate transcription in various events.

Keywords

Transcription, Genetic, Mediator Complex, RNA Polymerase II, Humans, Gene Expression Regulation, Protein Binding, Cyclin-Dependent Kinase 8, Models, Molecular, Mediator, CDK8 kinase module (CKM), core Mediator (cMED), Transcription, MED12, MED13, T-loop, RNA polymerase II (RNAPII), Pre-initiation complex (PIC)

Published Open-Access

yes

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.