Structural basis of Q-dependent antitermination

Proc Natl Acad Sci U S A. 2019 Sep 10;116(37):18384-18390. doi: 10.1073/pnas.1909801116. Epub 2019 Aug 27.

Abstract

Lambdoid bacteriophage Q protein mediates the switch from middle to late bacteriophage gene expression by enabling RNA polymerase (RNAP) to read through transcription terminators preceding bacteriophage late genes. Q loads onto RNAP engaged in promoter-proximal pausing at a Q binding element (QBE) and adjacent sigma-dependent pause element (SDPE) to yield a Q-loading complex, and Q subsequently translocates with RNAP as a pausing-deficient, termination-deficient Q-loaded complex. Here, we report high-resolution structures of 4 states on the pathway of antitermination by Q from bacteriophage 21 (Q21): Q21, the Q21-QBE complex, the Q21-loading complex, and the Q21-loaded complex. The results show that Q21 forms a torus, a "nozzle," that narrows and extends the RNAP RNA-exit channel, extruding topologically linked single-stranded RNA and preventing the formation of pause and terminator hairpins.

Keywords: RNA polymerase; transcription antitermination; transcription antitermination factor Q; transcription antitermination factor Q21; transcription elongation complex.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Bacterial Proteins / genetics
  • Bacteriophage lambda / genetics
  • Base Sequence
  • DNA-Directed RNA Polymerases / genetics
  • DNA-Directed RNA Polymerases / metabolism*
  • Escherichia coli / genetics
  • Gene Expression Regulation
  • Models, Molecular
  • Promoter Regions, Genetic
  • Protein Conformation
  • Recombinant Proteins
  • Terminator Regions, Genetic
  • Transcription, Genetic
  • Viral Proteins / chemistry*
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*

Substances

  • Bacterial Proteins
  • Q protein, Bacteriophage lambda
  • Recombinant Proteins
  • Viral Proteins
  • DNA-Directed RNA Polymerases

Associated data

  • PDB/6P1A
  • PDB/6P1C
  • PDB/6P18
  • PDB/6P19