Aili M, Telepnev M, Hallberg B, Wolf-Watz H, Rosqvist R.
In vitro GAP activity towards RhoA, Rac1 and Cdc42 is not a prerequisite for YopE induced HeLa cell cytotoxicity.
Microb Pathog. 2003 Jun;34(6):297-308
Abstract:
The YopE cytotoxin of Yersinia is an essential virulence determinant
that is translocated into the eukaryotic target cell via a
plasmid-encoded type III secretion system. YopE possess a GTPase
activating protein activity that in vitro has been shown to down
regulate RhoA, Rac1, and Cdc42. Translocated YopE induces
de-polymerisation of the actin microfilament structure in the
eukaryotic cell which results in a rounding up of infected cells
described as a cytotoxic effect. Here, we have investigated the
importance of different regions of YopE for induction of cytotoxicity
and in vitro GAP activity. Sequential removal of the N- and C-terminus
of YopE identified the region between amino acids 90 and 215 to be
necessary for induction of cytotoxicity. Internal deletions containing
the essential arginine at position 144 resulted in a total loss of
cytotoxic response. In-frame deletions flanking the arginine finger
defined a region important for the cytotoxic effect to amino acids
166-183. Four triple-alanine substitution mutants in this region,
YopE166-8A, 169-71A, 175-7A and 178-80A were still able to induce
cytotoxicity on HeLa cells although they did not show any in vitro GAP
activity towards RhoA, Rac1 or Cdc42. A substitution mutant in position
206-8A showed the same phenotype, ability to induce cytotoxic response
but no in vitro GAP activity. We speculate that YopE may have
additional unidentified targets within the eukaryotic cell.
DOI-Link
In vitro GAP activity towards RhoA, Rac1 and Cdc42 is not a prerequisite for YopE induced HeLa cell
- Details