Structures and compositional dynamics of Mediator in transcription regulation

Curr Opin Struct Biol. 2024 Oct:88:102892. doi: 10.1016/j.sbi.2024.102892. Epub 2024 Jul 26.

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.

Publication types

  • Review

MeSH terms

  • Cyclin-Dependent Kinase 8 / metabolism
  • Gene Expression Regulation*
  • Humans
  • Mediator Complex* / chemistry
  • Mediator Complex* / metabolism
  • Models, Molecular
  • Protein Binding
  • RNA Polymerase II* / chemistry
  • RNA Polymerase II* / metabolism
  • Transcription, Genetic*

Substances

  • Mediator Complex
  • RNA Polymerase II
  • Cyclin-Dependent Kinase 8