Home LiteratureArticle Details
PMID: 11157945 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Characterization of the dnaK multigene family in the Cyanobacterium Synechococcus sp. strain PCC7942.

Journal of bacteriology ·Vol. 183 ·No. 4 ·2001-02-00 ·Pages 1320-8

Nimura K, Takahashi H, Yoshikawa H

Abstract

The cyanobacterium Synechococcus sp. strain PCC7942 has three dnaK homologues (dnaK1, dnaK2, and dnaK3), and a gene disruption experiment was carried out for each dnaK gene by inserting an antibiotic resistance marker. Our findings revealed that DnaK1 was not essential for normal growth, whereas DnaK2 and DnaK3 were essential. We also examined the effect of heat shock on the levels of these three DnaK and GroEL proteins and found a varied response to heat shock, with levels depending on each protein. The DnaK2 and GroEL proteins exhibited a typical heat shock response, that is, their synthesis increased upon temperature upshift. In contrast, the synthesis of DnaK1 and DnaK3 did not respond to heat shock; in fact, the level of DnaK1 protein decreased. We also analyzed the effect of overproduction of each DnaK protein in Escherichia coli cells using an inducible expression system. Overproduction of DnaK1 or DnaK2 resulted in defects in cell septation and formation of cell filaments. On the other hand, overproduction of DnaK3 did not result in filamentous cells; rather a swollen and twisted cell morphology was observed. When expressed in an E. coli dnaK756 mutant, dnaK2 could suppress the growth deficiency at the nonpermissive temperature, while dnaK1 and dnaK3 could not suppress this phenotype. On the contrary, overproduction of DnaK1 or DnaK3 resulted in growth inhibition at the permissive temperature. These results suggest that different types of Hsp70 in the same cellular compartment have specific functions in the cell.

MeSH Terms
Chaperonin 60/biosynthesis Cyanobacteria/genetics DNA-Directed RNA Polymerases/genetics Escherichia coli/cytology Escherichia coli Proteins Genetic Complementation Test HSP70 Heat-Shock Proteins/biosynthesis,genetics Heat-Shock Response Molecular Chaperones/genetics Multigene Family Mutagenesis, Insertional Recombinant Proteins/biosynthesis Sigma Factor/genetics
Chemicals
Chaperonin 60 Escherichia coli Proteins HSP70 Heat-Shock Proteins Molecular Chaperones Recombinant Proteins Sigma Factor RNA polymerase sigma 70 DNA-Directed RNA Polymerases dnaK protein, E coli
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nimura K
Department of Bioscience, Tokyo University of Agriculture, Setagaya-ku, Tokyo 156-8502, Japan.
Takahashi H
Yoshikawa H
References (46)
46 references, click to expand
  1. The dnaK protein modulates the heat-shock response of Escherichia coli.
    Cell. 1983 Sep;34(2):641-6 PMID: 6311435
  2. Transposition and fusion of the lac genes to selected promoters in Escherichia coli using bacteriophage lambda and Mu.
    J Mol Biol. 1976 Jul 5;104(3):541-55 PMID: 781293
  3. Mutations of the heat inducible 70 kilodalton genes of yeast confer temperature sensitive growth.
    Cell. 1984 Oct;38(3):841-9 PMID: 6386178
  4. In vitro insertional mutagenesis with a selectable DNA fragment.
    Gene. 1984 Sep;29(3):303-13 PMID: 6237955
  5. Mutations in cognate genes of Saccharomyces cerevisiae hsp70 result in reduced growth rates at low temperatures.
    Mol Cell Biol. 1985 Dec;5(12):3517-24 PMID: 3915778
  6. Escherichia coli dnaK null mutants are inviable at high temperature.
    J Bacteriol. 1987 Jan;169(1):283-90 PMID: 3025174
  7. Complex interactions among members of an essential subfamily of hsp70 genes in Saccharomyces cerevisiae.
    Mol Cell Biol. 1987 Jul;7(7):2568-77 PMID: 3302682
  8. Proteins as molecular chaperones.
    Nature. 1987 Jul 30-Aug 5;328(6129):378-9 PMID: 3112578
  9. Sigma 32 synthesis can regulate the synthesis of heat shock proteins in Escherichia coli.
    Genes Dev. 1987 Apr;1(2):179-84 PMID: 3315848
  10. DNA transformation.
    Methods Enzymol. 1988;167:703-12 PMID: 3148838
  11. The heat-shock proteins.
    Annu Rev Genet. 1988;22:631-77 PMID: 2853609
  12. Cellular defects caused by deletion of the Escherichia coli dnaK gene indicate roles for heat shock protein in normal metabolism.
    J Bacteriol. 1989 May;171(5):2337-46 PMID: 2651398
  13. Yeast Hsp70 RNA levels vary in response to the physiological status of the cell.
    J Bacteriol. 1989 May;171(5):2680-8 PMID: 2651414
  14. Roles of Escherichia coli heat shock proteins DnaK, DnaJ and GrpE in mini-F plasmid replication.
    Mol Gen Genet. 1990 Jan;220(2):277-82 PMID: 2183004
  15. Regulation and sequence of the Synechococcus sp. strain PCC 7942 groESL operon, encoding a cyanobacterial chaperonin.
    J Bacteriol. 1990 Sep;172(9):5079-88 PMID: 1975581
  16. Role of Escherichia coli heat shock proteins DnaK and HtpG (C62.5) in response to nutritional deprivation.
    J Bacteriol. 1990 Dec;172(12):7157-66 PMID: 2254278
  17. DnaK, DnaJ, and GrpE heat shock proteins negatively regulate heat shock gene expression by controlling the synthesis and stability of sigma 32.
    Genes Dev. 1990 Dec;4(12A):2202-9 PMID: 2269429
  18. Molecular chaperones.
    Annu Rev Biochem. 1991;60:321-47 PMID: 1679318
  19. Protein folding in the cell.
    Nature. 1992 Jan 2;355(6355):33-45 PMID: 1731198
  20. Cloning, sequencing, and molecular analysis of the groESL operon of Clostridium acetobutylicum.
    J Bacteriol. 1992 May;174(10):3282-9 PMID: 1349602
  21. Cloning, sequencing, and molecular analysis of the dnaK locus from Bacillus subtilis.
    J Bacteriol. 1992 May;174(10):3300-10 PMID: 1339421
  22. Cloning and characterization of the groESL operon from Bacillus subtilis.
    J Bacteriol. 1992 Jun;174(12):3981-92 PMID: 1350776
  23. Cloning, sequencing, mapping, and transcriptional analysis of the groESL operon from Bacillus subtilis.
    J Bacteriol. 1992 Jun;174(12):3993-9 PMID: 1350777
  24. Physiological consequences of DnaK and DnaJ overproduction in Escherichia coli.
    J Bacteriol. 1992 Nov;174(22):7436-44 PMID: 1429465
  25. Isolation and characterization of the groES and groEL genes of Bacillus subtilis Marburg.
    Biosci Biotechnol Biochem. 1992 Dec;56(12):1995-2002 PMID: 1369494
  26. Regulation of the heat-shock response in bacteria.
    Annu Rev Microbiol. 1993;47:321-50 PMID: 7504905
  27. Enhancer activity of light-responsive regulatory elements in the untranslated leader regions of cyanobacterial psbA genes.
    Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11678-82 PMID: 8265608
  28. CIRCE, a novel heat shock element involved in regulation of heat shock operon dnaK of Bacillus subtilis.
    J Bacteriol. 1994 Mar;176(5):1359-63 PMID: 8113175
  29. A gene encoding a DnaK/hsp70 homolog in Escherichia coli.
    Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2066-70 PMID: 8134349
  30. Identification of dnaK multigene family in Synechococcus sp. PCC7942.
    Biochem Biophys Res Commun. 1994 May 30;201(1):466-71 PMID: 8198610
  31. Sequence analysis of the third dnaK homolog gene in Synechococcus sp. PCC7942.
    Biochem Biophys Res Commun. 1994 Jun 15;201(2):848-54 PMID: 8003021
  32. Hsc66, an Hsp70 homolog in Escherichia coli, is induced by cold shock but not by heat shock.
    J Bacteriol. 1995 Sep;177(17):4900-7 PMID: 7665466
  33. Regulation of groE expression in Bacillus subtilis: the involvement of the sigma A-like promoter and the roles of the inverted repeat sequence (CIRCE).
    J Bacteriol. 1995 Oct;177(19):5427-33 PMID: 7559325
  34. hrcA, the first gene of the Bacillus subtilis dnaK operon encodes a negative regulator of class I heat shock genes.
    J Bacteriol. 1996 Feb;178(4):1088-93 PMID: 8576042
  35. A cycle of binding and release of the DnaK, DnaJ and GrpE chaperones regulates activity of the Escherichia coli heat shock transcription factor sigma32.
    EMBO J. 1996 Feb 1;15(3):607-17 PMID: 8599944
  36. Molecular chaperones in cellular protein folding.
    Nature. 1996 Jun 13;381(6583):571-9 PMID: 8637592
  37. DnaK3, one of the three DnaK proteins of cyanobacterium Synechococcus sp. PCC7942, is quantitatively detected in the thylakoid membrane.
    Biochem Biophys Res Commun. 1996 Dec 4;229(1):334-40 PMID: 8954128
  38. Functional specificity among Hsp70 molecular chaperones.
    Science. 1997 Jan 17;275(5298):387-9 PMID: 8994035
  39. Sequence and analysis of a dnaJ homologue gene in cyanobacterium Synechococcus sp. PCC7942.
    Biochem Biophys Res Commun. 1997 Jul 18;236(2):461-6 PMID: 9240461
  40. The GroE chaperonin machine is a major modulator of the CIRCE heat shock regulon of Bacillus subtilis.
    EMBO J. 1997 Aug 1;16(15):4579-90 PMID: 9303302
  41. Genomic sequence of a Lyme disease spirochaete, Borrelia burgdorferi.
    Nature. 1997 Dec 11;390(6660):580-6 PMID: 9403685
  42. Hsc62, a new DnaK homologue of Escherichia coli.
    Biochem Biophys Res Commun. 1998 Sep 8;250(1):115-8 PMID: 9735342
  43. Regulation of the heat-shock response.
    Curr Opin Microbiol. 1999 Apr;2(2):153-8 PMID: 10322172
  44. Sequence analysis of the genome of the unicellular cyanobacterium Synechocystis sp. strain PCC6803. II. Sequence determination of the entire genome and assignment of potential protein-coding regions.
    DNA Res. 1996 Jun 30;3(3):109-36 PMID: 8905231
  45. Specificity crosstalk among group 1 and group 2 sigma factors in the cyanobacterium Synechococcus sp. PCC7942: In vitro specificity and a phylogenetic analysis.
    Mol Microbiol. 1999 Nov;34(3):473-84 PMID: 10564489
  46. A host-vector system for gene cloning in the cyanobacterium Anacystis nidulans R2.
    Plasmid. 1983 Sep;10(2):156-63 PMID: 6314409
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
2001-02-00
Pages
1320-8
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC95006
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]