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Characterization of a four-member psbA gene family from the cyanobacterium Anabaena PCC 7120

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Abstract

The cyanobacterium Anabaena PCC 7120 contains a multigene family that encodes the D1 polypeptide of Photosystem II. This family consists of four members denoted psbAI-IV that are each unique but highly homologous. psbAII, III and IV are more closely related to each other than to psbAI. These three copies encode identical polypeptides that differ from the psbAI product by 21 amino acids. The transcription initiation site for psbAI has been mapped to 64–65 nucleotides upstream from the coding region. Primer extension assays performed with an oligonucleotide specific for psbAII, III and IV transcripts suggest that one or more of these genes is also expressed. Genomic mapping and chromosome walking experiments demonstrate that none of the four psbA copies is within 20 kbp of another member of the gene family.

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References

  1. Alam J, Whitaker RA, Krogmann DW, Curtis SE: Isolation and sequence of the gene for ferredoxin I from the cyanobacterium Anabaena sp. strain PCC 7120. J Bact 168: 1265–1271 (1986).

    PubMed  Google Scholar 

  2. Brosius J, Dull TJ, Sleeter DD, Noller HF: Gene organization and primary structure of a ribosomal RNA operon from Escherichia coli. J Mol Biol 148: 107–127 (1981).

    PubMed  Google Scholar 

  3. Brusslan J, Haselkorn R: Resistance to the photosystem II herbicide diuron is dominant to sensitivity in the cyanobacterium Synechococcus sp. PCC 7942. EMBO J 8: 1237–1245 (1989).

    Google Scholar 

  4. Bryant DA: The cyanobacterial photosynthetic apparatus: comparison of those of higher plants and photosynthetic bacteria. In: Platt T, Li WKW (eds) Photosynthetic Picoplankton, pp. 423–500, Canadian Bulletin of Fisheries and Aquatic Science, vol 214. Department of Fisheries and Oceans, Ottawa (1986).

    Google Scholar 

  5. Curtis SE, Haselkorn R: Isolation and sequence of the gene for the large subunit of ribulose-1,5-bisphosphate carboxylase from the cyanobacterium Anabaena 7120. Proc Natl Acad Sci USA 80: 1835–1839 (1983).

    Google Scholar 

  6. Curtis SE, Haselkorn R: Isolation, sequence and expression of two members of the 32kd thylakoid membrane protein gene family from the cyanobacterium Anabaena 7120. Plant Mol Biol 3: 249–258 (1984).

    Google Scholar 

  7. Curtis SE: Genes encoding the beta and epsilon subunits of the proton-translocating ATPase from Anabaena sp. strain PCC 7120. J Bact 169: 80–86 (1987).

    PubMed  Google Scholar 

  8. Dayhoff MO, Schwartz RM, Orcutt BC: A model of evolutionary change in proteins. In: Dayhoff MO (ed) Atlas of Protein Sequence and Structure, vol 5, pp. 345–352. National Biomedical Research Foundation, Washington, D.C. (1978).

    Google Scholar 

  9. Debus RJ, Barry BA, Sithole I, Babcock GT, McIntosh L: Directed mutagenesis indicates that the donor to P680 in photosystem II is tyrosine-161 of the D1 polypeptide. Biochemistry 27: 9071–9074 (1988).

    PubMed  Google Scholar 

  10. Eyal Y, Goloubinoff P, Edelman M: The amino terminal region delimited by Met1, and Met37 is an integral part of the 32 kDa herbicide binding protein. Plant Mol Biol 8: 337–343 (1987).

    Google Scholar 

  11. Gingrich JC, Buzby JS, Stirewalt VL, Bryant DA: Genetic analysis of two new mutations resulting in herbicide resistance in the cyanobacterium Synechococcus sp. PCC 7002. Photosynth Res 16: 83–99 (1988).

    Google Scholar 

  12. Golden SS, Brusslan JA, Haselkorn R: Expression of a family of psbA genes encoding a photosystem II polypeptide in the cyanobacterium Anacystis nidulans R2. EMBO J 5: 2789–2798 (1986).

    PubMed  Google Scholar 

  13. Gruissem W, Barkan A, Deng X-W, Stern D: Transcriptional and postranscriptional control of plastid mRNA levels in plants. Trends Genet 4: 258–263 (1988).

    Article  PubMed  Google Scholar 

  14. Herrero A, Wolk P: Genetic mapping of the chromosome of the cyanobacterium Anabaena variabilis. J Biol Chem 261: 7748–7754 (1986).

    PubMed  Google Scholar 

  15. Jannson CRJ, Debus J, Osiewacz HD, Gurevitz M, McIntosh L: Construction of an obligate photoheterotrophic mutant of the cyanobacterium Synechocystis 6803. Plant Physiol 85: 1021–1025 (1987).

    Google Scholar 

  16. Maniatis T, Fritsch EF, Sambrook J: Molecular Cloning: A Laboratory Manual, pp. 270–281, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1982).

    Google Scholar 

  17. Marder JB, Chapman DJ, Telfer A, Nixon PJ, Barber J: Identification of psbA and psbD gene products, D1 and D2, as reaction centre proteins of photosystem 2. Plant Mol Biol 9: 206–210 (1987).

    Google Scholar 

  18. McCarn DF, Whitaker RA, Alam JA, Vrba JM, Curtis SE: Genes encoding the alpha, gamma, delta, and four Fo subunits of ATP synthase constitute an operon in the cyanobacterium Anabaena sp. PCC 7120. J Bact 170: 3448–3458 (1988).

    PubMed  Google Scholar 

  19. Michel H, Deisenhofer J: Relevance of the photosynthetic reaction center from purple bacteria to the structure of photosystem II. Biochemistry 27: 1–7 (1988).

    Google Scholar 

  20. Mulligan B, Schulters N, Chen L, Bogoard L: Nucleotide sequence of a multiple-copy gene for the B protein of photosystem II of a cyanobacterium. Proc Natl Acad Sci USA 81: 2693–2697 (1984).

    Google Scholar 

  21. Nanba O, Satoh O: Isolation of a photosystem II reaction center consisting of D-1 and D-2 polypeptides and cytochrome b-559. Proc Natl Acad Sci USA 84: 109–112 (1987).

    Google Scholar 

  22. Newbury SF, Smith NH, Robinson EC, Hiles ID, Higgins CF: Stabilization of translationally active mRNA by prokaryotic REP sequences. Cell 48: 297–310 (1987).

    Article  PubMed  Google Scholar 

  23. Nierzwicki-Bauer SA, Curtis SE, Haselkorn R: Cotranscription of genes encoding the small and large subunits of ribulose-1,5-bisphosphate carboxylase in the cyanobacterium Anabaena 7120. Proc Natl Acad Sci USA 81: 5961–5965 (1984).

    PubMed  Google Scholar 

  24. Nierwicki-Bauer SA, Haselkorn R: Differences in mRNA levels in Anabaena living freely or in symbiotic association with Azolla. EMBO J 5: 29–35 (1986).

    PubMed  Google Scholar 

  25. Palmer JD: Comparative organization of chloroplast genomes. Ann Rev Genet 9: 325–354 (1985).

    Article  Google Scholar 

  26. Platt T: Transcription termination and the regulation of gene expression. Ann Rev Biochem 55: 339–372 (1986).

    Article  PubMed  Google Scholar 

  27. Reznikoff WS, Siegele DA, Cowing DA, Gross CA: The regulation of transcription initiation in bacteria. Ann Rev Genet 9: 355–388 (1985).

    Article  Google Scholar 

  28. Rice D, Mazur BJ, Haselkorn R: Isolation and physical mapping of nitrogen fixation genes from the cyanobacterium Anabaena 7120. J Biol Chem 257: 13157–13167 (1982).

    PubMed  Google Scholar 

  29. Sanger F, Nicklen S, Coulson AR: DNA sequencing with chaintermination inhibitors. Proc Natl Acad Sci USA 74: 5463–5467 (1977).

    PubMed  Google Scholar 

  30. Schneider GJ, Tumer NE, Richaud C, Borbely G, Haselkorn R: Purification and characterization of RNA polymerase from the cyanobacterium Anabaena 7120. J Biol Chem 262: 14633–14639 (1987).

    PubMed  Google Scholar 

  31. Shaefer MR, Golden S: Light availability influences the ratio of two forms of D1 in cyanobacterial thylakoids. J Biol Chem 264: 7412–7417 (1989).

    PubMed  Google Scholar 

  32. Shine J, Dalgarno L: The 3′-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites. Proc Natl Acad Sci USA 71: 1342–1346 (1974).

    PubMed  Google Scholar 

  33. Tinoco IJr, Borer PN, Dengler B, Levine M, Uhlenbeck OC, Crothers DM, Gralla J: Improved estimation of secondary structure in ribonucleic acids. Nature 246: 40–41 (1973).

    Google Scholar 

  34. Trebst A: The topology of the plastoquinone and herbicide binding peptides of photosystem II in the thylakoid membrane. Z Naturforsch 41c: 240–245 (1986).

    Google Scholar 

  35. Tumer NE, Robinson SJ, Haselkorn R: Different promoters for the Anabaena glutamine synthetase gene during growth using molecular or fixed nitrogen. Nature 306: 337–341 (1983).

    Google Scholar 

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Vrba, J.M., Curtis, S.E. Characterization of a four-member psbA gene family from the cyanobacterium Anabaena PCC 7120. Plant Mol Biol 14, 81–92 (1990). https://doi.org/10.1007/BF00015657

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