Structural basis for the recognition of the S2, S5-phosphorylated RNA polymerase II CTD by the mRNA anti-terminator protein hSCAF4

FEBS Lett. 2022 Jan;596(2):249-259. doi: 10.1002/1873-3468.14256. Epub 2021 Dec 20.

Abstract

The C-terminal domain (CTD) of RNA polymerase II serves as a binding platform for numerous enzymes and transcription factors involved in nascent RNA processing and the transcription cycle. The S2, S5-phosphorylated CTD is recognized by the transcription factor SCAF4, which functions as a transcription anti-terminator by preventing early mRNA transcript cleavage and polyadenylation. Here, we measured the binding affinities of differently modified CTD peptides by hSCAF4 and solved the complex structure of the hSCAF4-CTD-interaction domain (CID) bound to a S2, S5-quadra-phosphorylated CTD peptide. Our results revealed that the S2, S5-quadra-phosphorylated CTD peptide adopts a trans conformation and is located in a positively charged binding groove of hSCAF4-CID. Although hSCAF4-CID has almost the same binding pattern to the CTD as other CID-containing proteins, it preferentially binds to the S2, S5-phosphorylated CTD. Our findings provide insight into the regulatory mechanism of hSCAF4 in transcription termination.

Keywords: CTD interaction domain; X-ray crystallography; hSCAF4; isothermal titration calorimetry; phosphorylated CTD.

MeSH terms

  • Binding Sites
  • Humans
  • Models, Molecular
  • Phosphorylation
  • Protein Binding*
  • Protein Domains
  • RNA Polymerase II* / chemistry
  • RNA Polymerase II* / genetics
  • RNA Polymerase II* / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Saccharomyces cerevisiae
  • Serine-Arginine Splicing Factors*
  • Transcription Factors / chemistry
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription Termination, Genetic

Substances

  • RNA Polymerase II
  • RNA, Messenger
  • Transcription Factors
  • SCAF4 protein, human
  • Serine-Arginine Splicing Factors

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