A translocator-specific export signal establishes the translocator-effector secretion hierarchy that is important for type III secretion system function

Mol Microbiol. 2012 Dec;86(6):1464-81. doi: 10.1111/mmi.12069. Epub 2012 Nov 5.

Abstract

Type III secretion systems are used by many Gram-negative pathogens to directly deliver effector proteins into the cytoplasm of host cells. To accomplish this, bacteria secrete translocator proteins that form a pore in the host-cell membrane through which the effector proteins are then introduced into the host cell. Evidence from multiple systems indicates that the pore-forming translocator proteins are exported before effectors, but how this secretion hierarchy is established is unclear. Here we used the Pseudomonas aeruginosa translocator protein PopD as a model to identify its export signals. The N-terminal secretion signal and chaperone, PcrH, are required for export under all conditions. Two novel signals in PopD, one proximal to the chaperone binding site and one at the very C-terminus of the protein, are required for export of PopD before effector proteins. These novel export signals establish the translocator-effector secretion hierarchy, which in turn, is critical for the delivery of effectors into host cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Secretion Systems / genetics*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism*
  • Models, Biological
  • Protein Sorting Signals
  • Protein Transport
  • Pseudomonas aeruginosa / genetics
  • Pseudomonas aeruginosa / metabolism*

Substances

  • Bacterial Secretion Systems
  • Membrane Transport Proteins
  • Protein Sorting Signals