Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1995 Apr;177(8):2080–2086. doi: 10.1128/jb.177.8.2080-2086.1995

Bacterial luciferase as a reporter of circadian gene expression in cyanobacteria.

Y Liu 1, S S Golden 1, T Kondo 1, M Ishiura 1, C H Johnson 1
PMCID: PMC176852  PMID: 7536731

Abstract

To allow continuous monitoring of the circadian clock in cyanobacteria, we previously created a reporter strain (AMC149) of Synechococcus sp. strain PCC 7942 in which the promoter of the psbAI gene was fused to Vibrio harveyi luciferase structural genes (luxAB) and integrated into the chromosome. Northern (RNA) hybridization and immunoblot analyses were performed to examine changes in abundance of the luxAB mRNA, the native psbAI mRNA, and the luciferase protein to determine whether bioluminescence is an accurate reporter of psbAI promoter activity in AMC149. Under constant light conditions, the mRNA abundances of both luxAB and psbAI oscillated with a period of approximately 24 h for at least 2 days. The expression of these two genes following the same pattern: both mRNAs peaked in the subjective morning, and their troughs occurred near the end of the subjective night. The amount of luciferase protein also oscillated with a period of approximately 24 h, and the protein rhythm is in phase with the bioluminescence rhythm. The rhythm of the luciferase mRNA phase-leads the rhythms of luciferase protein and in vivo bioluminescence by several hours. Comparable results were obtained with a short-period mutant of AMC149. Together, these results indicate that the bioluminescence rhythm in AMC149 is due primarily to circadian oscillation of psbAI promoter activity in this cyanobacterium.

Full Text

The Full Text of this article is available as a PDF (392.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bustos S. A., Golden S. S. Expression of the psbDII gene in Synechococcus sp. strain PCC 7942 requires sequences downstream of the transcription start site. J Bacteriol. 1991 Dec;173(23):7525–7533. doi: 10.1128/jb.173.23.7525-7533.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cohn D. H., Mileham A. J., Simon M. I., Nealson K. H., Rausch S. K., Bonam D., Baldwin T. O. Nucleotide sequence of the luxA gene of Vibrio harveyi and the complete amino acid sequence of the alpha subunit of bacterial luciferase. J Biol Chem. 1985 May 25;260(10):6139–6146. [PubMed] [Google Scholar]
  3. González-Flecha B., Demple B. Intracellular generation of superoxide as a by-product of Vibrio harveyi luciferase expressed in Escherichia coli. J Bacteriol. 1994 Apr;176(8):2293–2299. doi: 10.1128/jb.176.8.2293-2299.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Jacobshagen S., Johnson C. H. Circadian rhythms of gene expression in Chlamydomonas reinhardtii: circadian cycling of mRNA abundances of cab II, and possibly of beta-tubulin and cytochrome c. Eur J Cell Biol. 1994 Jun;64(1):142–152. [PubMed] [Google Scholar]
  5. Johnston T. C., Thompson R. B., Baldwin T. O. Nucleotide sequence of the luxB gene of Vibrio harveyi and the complete amino acid sequence of the beta subunit of bacterial luciferase. J Biol Chem. 1986 Apr 15;261(11):4805–4811. [PubMed] [Google Scholar]
  6. Kay S. A. Shedding light on clock controlled cab gene transcription in higher plants. Semin Cell Biol. 1993 Apr;4(2):81–86. doi: 10.1006/scel.1993.1010. [DOI] [PubMed] [Google Scholar]
  7. Kippert F. Endocytobiotic coordination, intracellular calcium signaling, and the origin of endogenous rhythms. Ann N Y Acad Sci. 1987;503:476–495. doi: 10.1111/j.1749-6632.1987.tb40631.x. [DOI] [PubMed] [Google Scholar]
  8. Kondo T., Ishiura M. Circadian rhythms of cyanobacteria: monitoring the biological clocks of individual colonies by bioluminescence. J Bacteriol. 1994 Apr;176(7):1881–1885. doi: 10.1128/jb.176.7.1881-1885.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kondo T., Strayer C. A., Kulkarni R. D., Taylor W., Ishiura M., Golden S. S., Johnson C. H. Circadian rhythms in prokaryotes: luciferase as a reporter of circadian gene expression in cyanobacteria. Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5672–5676. doi: 10.1073/pnas.90.12.5672. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kondo T., Tsinoremas N. F., Golden S. S., Johnson C. H., Kutsuna S., Ishiura M. Circadian clock mutants of cyanobacteria. Science. 1994 Nov 18;266(5188):1233–1236. doi: 10.1126/science.7973706. [DOI] [PubMed] [Google Scholar]
  11. Kulkarni R. D., Golden S. S. Adaptation to high light intensity in Synechococcus sp. strain PCC 7942: regulation of three psbA genes and two forms of the D1 protein. J Bacteriol. 1994 Feb;176(4):959–965. doi: 10.1128/jb.176.4.959-965.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kulkarni R. D., Schaefer M. R., Golden S. S. Transcriptional and posttranscriptional components of psbA response to high light intensity in Synechococcus sp. strain PCC 7942. J Bacteriol. 1992 Jun;174(11):3775–3781. doi: 10.1128/jb.174.11.3775-3781.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Mattoo A. K., Hoffman-Falk H., Marder J. B., Edelman M. Regulation of protein metabolism: Coupling of photosynthetic electron transport to in vivo degradation of the rapidly metabolized 32-kilodalton protein of the chloroplast membranes. Proc Natl Acad Sci U S A. 1984 Mar;81(5):1380–1384. doi: 10.1073/pnas.81.5.1380. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Millar A. J., Short S. R., Chua N. H., Kay S. A. A novel circadian phenotype based on firefly luciferase expression in transgenic plants. Plant Cell. 1992 Sep;4(9):1075–1087. doi: 10.1105/tpc.4.9.1075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Nanba O., Satoh K. Isolation of a photosystem II reaction center consisting of D-1 and D-2 polypeptides and cytochrome b-559. Proc Natl Acad Sci U S A. 1987 Jan;84(1):109–112. doi: 10.1073/pnas.84.1.109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ohad I., Kyle D. J., Arntzen C. J. Membrane protein damage and repair: removal and replacement of inactivated 32-kilodalton polypeptides in chloroplast membranes. J Cell Biol. 1984 Aug;99(2):481–485. doi: 10.1083/jcb.99.2.481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Pittendrigh C. S. Temporal organization: reflections of a Darwinian clock-watcher. Annu Rev Physiol. 1993;55:16–54. doi: 10.1146/annurev.ph.55.030193.000313. [DOI] [PubMed] [Google Scholar]
  18. Schaefer M. R., Golden S. S. Differential expression of members of a cyanobacterial psbA gene family in response to light. J Bacteriol. 1989 Jul;171(7):3973–3981. doi: 10.1128/jb.171.7.3973-3981.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Spector T. Refinement of the coomassie blue method of protein quantitation. A simple and linear spectrophotometric assay for less than or equal to 0.5 to 50 microgram of protein. Anal Biochem. 1978 May;86(1):142–146. doi: 10.1016/0003-2697(78)90327-5. [DOI] [PubMed] [Google Scholar]
  20. Waters C. A., Hastings J. W. Mutants of luminous bacteria with an altered control of luciferase synthesis. J Bacteriol. 1977 Aug;131(2):519–525. doi: 10.1128/jb.131.2.519-525.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES