The sigmaE and Cpx regulatory pathways: overlapping but distinct envelope stress responses.

The Cpx and sigmaE extracytoplasmic stress responses sense and respond to misfolded proteins in the bacterial envelope. Recent studies have highlighted differences between these regulatory pathways in terms of activating signals, mechanisms of signal transduction and the nature of the responses. Cumulatively, the findings suggest distinct physiological roles for these partially overlapping envelope stress responses. The sigmaE pathway is essential for survival and is primarily responsible for monitoring and responding to alterations in outer membrane protein folding. Mounting evidence suggests that the Cpx regulon may have been adapted to ensure properly timed expression and assembly of adhesive organelles.

[1]  S. Raina,et al.  A new heat‐shock gene, ppiD, encodes a peptidyl–prolyl isomerase required for folding of outer membrane proteins in Escherichia coli , 1998, The EMBO journal.

[2]  R. Taylor,et al.  Characterization of a periplasmic thiol:disulfide interchange protein required for the functional maturation of secreted virulence factors of Vibrio cholerae. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[3]  W. B. Snyder,et al.  The Cpx two-component signal transduction pathway of Escherichia coli regulates transcription of the gene specifying the stress-inducible periplasmic protease, DegP. , 1995, Genes & development.

[4]  D. Martin,et al.  Analysis of promoters controlled by the putative sigma factor AlgU regulating conversion to mucoidy in Pseudomonas aeruginosa: relationship to sigma E and stress response , 1994, Journal of bacteriology.

[5]  V. Deretic,et al.  Control of AlgU, a member of the sigma E-like family of stress sigma factors, by the negative regulators MucA and MucB and Pseudomonas aeruginosa conversion to mucoidy in cystic fibrosis , 1996, Journal of bacteriology.

[6]  J. Liu,et al.  Peptidyl-prolyl cis-trans-isomerase from Escherichia coli: a periplasmic homolog of cyclophilin that is not inhibited by cyclosporin A. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[7]  C. Gross,et al.  The activity of sigma 32 is reduced under conditions of excess heat shock protein production in Escherichia coli. , 1989, Genes & development.

[8]  T. Donohue,et al.  The activity of sigma E, an Escherichia coli heat-inducible sigma-factor, is modulated by expression of outer membrane proteins. , 1993, Genes & development.

[9]  J. Beckwith,et al.  Characterization of degP, a gene required for proteolysis in the cell envelope and essential for growth of Escherichia coli at high temperature , 1989, Journal of bacteriology.

[10]  T. Silhavy,et al.  The chaperone‐assisted membrane release and folding pathway is sensed by two signal transduction systems , 1997, The EMBO journal.

[11]  B. Bukau Regulation of the Escherichia coli heat‐shock response , 1993, Molecular microbiology.

[12]  T. Silhavy,et al.  CpxP, a Stress-Combative Member of the Cpx Regulon , 1998, Journal of bacteriology.

[13]  E. Lin,et al.  The deduced amino-acid sequence of the cloned cpxR gene suggests the protein is the cognate regulator for the membrane sensor, CpxA, in a two-component signal transduction system of Escherichia coli. , 1993, Gene.

[14]  R. Kolter,et al.  SurA assists the folding of Escherichia coli outer membrane proteins , 1996, Journal of bacteriology.

[15]  S. Nakayama,et al.  Involvement of cpxA, a sensor of a two-component regulatory system, in the pH-dependent regulation of expression of Shigella sonnei virF gene , 1995, Journal of bacteriology.

[16]  D. Ohman,et al.  Mucoid-to-nonmucoid conversion in alginate-producing Pseudomonas aeruginosa often results from spontaneous mutations in algT, encoding a putative alternate sigma factor, and shows evidence for autoregulation , 1994, Journal of bacteriology.

[17]  C. Georgopoulos,et al.  Autoregulation of the Escherichia coli heat shock response by the DnaK and DnaJ heat shock proteins. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[18]  Induction and evasion of host defenses by type 1-piliated uropathogenic Escherichia coli. , 1998 .

[19]  C. Georgopoulos,et al.  Identification, characterization, and mapping of the Escherichia coli htrA gene, whose product is essential for bacterial growth only at elevated temperatures , 1989, Journal of bacteriology.

[20]  C. Georgopoulos,et al.  Modulation of the Escherichia coliσE (RpoE) heat‐shock transcription‐factor activity by the RseA, RseB and RseC proteins , 1997, Molecular microbiology.

[21]  K. Rudd,et al.  rpoE, the gene encoding the second heat‐shock sigma factor, sigma E, in Escherichia coli. , 1995, The EMBO journal.

[22]  C. Gross,et al.  SigmaE is an essential sigma factor in Escherichia coli , 1997, Journal of bacteriology.

[23]  C. Georgopoulos,et al.  The HtrA (DegP) protein, essential for Escherichia coli survival at high temperatures, is an endopeptidase , 1990, Journal of bacteriology.

[24]  T. Silhavy,et al.  The sigma(E) and the Cpx signal transduction systems control the synthesis of periplasmic protein-folding enzymes in Escherichia coli. , 1997, Genes & development.

[25]  Koreaki Ito,et al.  Identification and characterization of an Escherichia coli gene required for the formation of correctly folded alkaline phosphatase, a periplasmic enzyme. , 1992, The EMBO journal.

[26]  T. Galitski,et al.  The DnaK chaperone modulates the heat shock response of Escherichia coli by binding to the sigma 32 transcription factor. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[27]  J. Beckwith,et al.  An Escherichia coli mutation preventing degradation of abnormal periplasmic proteins. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[28]  E. Craig,et al.  Heat shock proteins: molecular chaperones of protein biogenesis , 1993, Microbiological reviews.

[29]  W. B. Snyder,et al.  Overproduction of NlpE, a new outer membrane lipoprotein, suppresses the toxicity of periplasmic LacZ by activation of the Cpx signal transduction pathway , 1995, Journal of bacteriology.

[30]  S. Hultgren,et al.  The chaperone/usher pathway: a major terminal branch of the general secretory pathway. , 1998, Current opinion in microbiology.

[31]  C. Gross,et al.  SurA, a periplasmic protein with peptidyl-prolyl isomerase activity, participates in the assembly of outer membrane porins. , 1996, Genes & development.

[32]  C. Gross,et al.  DnaK, DnaJ, and GrpE heat shock proteins negatively regulate heat shock gene expression by controlling the synthesis and stability of sigma 32. , 1990, Genes & development.

[33]  W. B. Snyder,et al.  Mutational activation of the Cpx signal transduction pathway of Escherichia coli suppresses the toxicity conferred by certain envelope‐associated stresses , 1995, Molecular microbiology.

[34]  P. Silverman,et al.  The cpx proteins of Escherichia coli K12. Structure of the cpxA polypeptide as an inner membrane component. , 1988, Journal of molecular biology.

[35]  D. Belin,et al.  A pathway for disulfide bond formation in vivo. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[36]  J. Betton,et al.  New components of protein folding in extracytoplasmic compartments of Escherichia coli SurA, FkpA and Skp/OmpH , 1996, Molecular microbiology.

[37]  C. Georgopoulos,et al.  The rpoE gene encoding the sigma E (sigma 24) heat shock sigma factor of Escherichia coli. , 1995, The EMBO journal.

[38]  R. Sauer,et al.  The DegP and DegQ periplasmic endoproteases of Escherichia coli: specificity for cleavage sites and substrate conformation , 1996, Journal of bacteriology.

[39]  D. Martin,et al.  Characterization of a locus determining the mucoid status of Pseudomonas aeruginosa: AlgU shows sequence similarities with a Bacillus sigma factor , 1993, Journal of bacteriology.

[40]  T. Silhavy,et al.  Transduction of envelope stress in Escherichia coli by the Cpx two-component system , 1997, Journal of bacteriology.

[41]  F. Jacob-Dubuisson,et al.  PapD chaperone function in pilus biogenesis depends on oxidant and chaperone-like activities of DsbA. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[42]  C. Georgopoulos,et al.  Sequence analysis and regulation of the htrA gene of Escherichia coli: a sigma 32-independent mechanism of heat-inducible transcription. , 1988, Nucleic acids research.

[43]  C. Gross,et al.  The σE‐mediated response to extracytoplasmic stress in Escherichia coli is transduced by RseA and RseB, two negative regulators of σE , 1997, Molecular microbiology.

[44]  W. Dowhan,et al.  The Cpx two-component signal transduction pathway is activated in Escherichia coli mutant strains lacking phosphatidylethanolamine , 1997, Journal of bacteriology.

[45]  J. Pogliano,et al.  Regulation of Escherichia coli cell envelope proteins involved in protein folding and degradation by the Cpx two-component system. , 1997, Genes & development.

[46]  T. Silhavy,et al.  Accumulation of the Enterobacterial Common Antigen Lipid II Biosynthetic Intermediate StimulatesdegP Transcription in Escherichia coli , 1998, Journal of bacteriology.

[47]  J. Kaguni,et al.  A novel sigma factor is involved in expression of the rpoH gene of Escherichia coli , 1989, Journal of bacteriology.

[48]  A. Chakrabarty,et al.  Sigma factor-anti-sigma factor interaction in alginate synthesis: inhibition of AlgT by MucA , 1996, Journal of bacteriology.

[49]  C. Gross,et al.  The response to extracytoplasmic stress in Escherichia coli is controlled by partially overlapping pathways. , 1997, Genes & development.

[50]  S. Hultgren,et al.  The PapG adhesin of uropathogenic Escherichia coli contains separate regions for receptor binding and for the incorporation into the pilus. , 1989, Proceedings of the National Academy of Sciences of the United States of America.