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Architecture of the RNA polymerase II-TFIIS complex and implications for mRNA cleavage.

The transcription elongation factor TFIIS induces mRNA cleavage by enhancing the intrinsic nuclease activity of RNA polymerase (Pol) II. We have diffused TFIIS into Pol II crystals and derived a model of the Pol II-TFIIS complex from X-ray diffraction data to 3.8 A resolution. TFIIS extends from the polymerase surface via a pore to the internal active site, spanning a distance of 100 A. Two essential and invariant acidic residues in a TFIIS loop complement the Pol II active site and could position a metal ion and a water molecule for hydrolytic RNA cleavage. TFIIS also induces extensive structural changes in Pol II that would realign nucleic acids in the active center. Our results support the idea that Pol II contains a single tunable active site for RNA polymerization and cleavage, in contrast to DNA polymerases with two separate active sites for DNA polymerization and cleavage.

Pubmed ID: 12914699


  • Kettenberger H
  • Armache KJ
  • Cramer P



Publication Data

August 8, 2003

Associated Grants


Mesh Terms

  • Amino Acid Sequence
  • Binding Sites
  • Crystallography, X-Ray
  • Fungal Proteins
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Multienzyme Complexes
  • Protein Binding
  • Protein Structure, Quaternary
  • RNA Polymerase II
  • RNA, Messenger
  • Sequence Alignment
  • Transcription Factors, General
  • Transcriptional Elongation Factors