Skip to main content
Log in

Activity of the promoter of the Lhca3.St.1 gene, encoding the potato apoprotein 2 of the light-harvesting complex of Photosystem I, in transgenic potato and tobacco plants

  • Short Communication
  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

We have isolated cDNA and genomic clones for the potato (Solanum tuberosum) apoprotein 2 of the light harvesting complex of Photosystem I, designated Lhca3.St.1. The protein shows all characteristics of the family of chlorophyll a/b-binding proteins. Potato Lhca3.1 gene expression occurs predominantly in leaves, and is transcriptionally regulated by light. One gene copy is present per haploid genome. The sequence of the 5′ upstream region was determined. Most boxes identified in the promoter sequences of genes whose expression is light-regulated recur in the Lhca3.St.1 sequence. Functional analyses of the Lhca3.St.1 promoter and two deletion derivatives in transgenic potato transformed with a promoter-GUS fusion show high promoter activity in leaves and other green parts of the plant, which depends on light. Activity is absent in roots and potato tubers. The 500 bp promoter fragment is as active as the full 2.0 kb sequence, showing that all regulatory elements are present on the smallest deletion derivative. In transgenic tobacco (Nicotiana tabacum) plants carrying the largest promoter derivative a similar distribution of activity is found. Promoter activity is not restricted to the phloem, but also prominent in the xylem of the young stem, which contrasts with promoters of other photosynthesis-associated genes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Aoyagi K, Kuhlemeier C, Chua NH: The pea rbcS-3A enhancer-like element directs cell-specific expression in transgenic tobacco. Mol Gen Gen 213: 179–185 (1988).

    Google Scholar 

  2. Ayers GS: Structure and anatomy of the tobacco leaf. Am J Bot 20: 565–593 (1933).

    Google Scholar 

  3. Bichler J, Herrmann RG: Analysis of the promoters of the single-copy genes for plastocyanin and subunit δ of the chloroplast ATP synthase from spinach Eur J Biochem 190: 415–426 (1990).

    Google Scholar 

  4. Bonierbale MW, Plaisted RL, Tanksley SD: RFLP maps based on a common set of clones reveal modes of chromosomal evolution in potato and tomato. Genetics 120: 1095–1103 (1988).

    Google Scholar 

  5. Castresana C, Garcia-Luque I, Alonso E, Malik VS, Cashmore AR: Both positive and negative regulatory elements mediate expression of a photoregulated CAB gene from Nicotiana plumbaginifolia. EMBO J 7: 1929–1936 (1988).

    Google Scholar 

  6. Chory J, Peto C, Feinbaum R, Pratt L, Ausubel F: Arabidopsis thaliana mutant that develops as a light-grown plant the absence of light. Cell 58: 991–999 (1989).

    Google Scholar 

  7. Deng X-W, Caspar T, Quail PH: cop 1: a regulatory locus involved in light-controlled development and gene expression in Arabidopsis. Genes Devel 5: 1172–1182 (1991).

    Google Scholar 

  8. DeBlock M, Debrouwer D: In-situ enzyme histochemistry on plastic-embedded plant material. The development of an artifact-free β-glucuronidase assay. Plant J 2: 261–266 (1992).

    Google Scholar 

  9. deVries SC, Harmsen MC, Kuiper MTR, Dons JJM, Wessels JGH: Molecular cloning of pea mRNAs encoding a shoot-specific polypeptide and light-induced polypeptides. Plant Mol Biol 2: 295–303 (1983).

    Google Scholar 

  10. Dupree P, Pwee KH, Gray JC: Expression of photosynthesis gene-promoter fusions in leaf epidermal cells of transgenic tobacco plants. Plant J 1: 115–120 (1991).

    Google Scholar 

  11. Gavel Y, vonHeijne G: A conserved cleavage-site motif in chloroplast transit peptide. FEBS Lett 261: 455–458 (1990).

    Google Scholar 

  12. Gilmartin PM, Chua N-H: Spacing between GT-1 binding sites within a light-responsive element is critical for transcriptional activity. Plant Cell 2: 477–455 (1990).

    Google Scholar 

  13. Gilmartin PM, Sarokin L, Memelink J, Chua N-H: Molecular light switches for plant genes. Plant Cell 2: 369–378 (1990).

    Google Scholar 

  14. Giuliano G, Hoffman NE, Ko K, Scolnik PA, Cashmore AR. A light-entrained circadian clock controls transcription of several plant genes. EMBO J 7: 3635–3642 (1988).

    Google Scholar 

  15. Green BR, Pichersky E, Kloppstech K: Chlorophyll a/b-binding proteins: an extended family. Trends Biochem Sci 16: 181–186 (1991).

    Google Scholar 

  16. Hageman J, Baecke C, Ebskamp M, Pilon R, Smeekens S, Weisbeek P: Protein import into and sorting inside the chloroplast are independent processes. Plant Cell 2: 479–494 (1990).

    Google Scholar 

  17. Herrmann RG, Oelm Üller R, Bichler J, Schneidebauer A, Steppuhn J, Wedel N, Tyagi AK, Westhoff P: The thylakoid membrane of higher plants: genes, their expression and interaction. In: Herrmann RG, Larkins BG (eds) Plant Molecular Biology, vol. 2, pp. 411–427. Plenum Press, New York (1991).

    Google Scholar 

  18. Jansson S, Gustafsson P: Evolutionary conservation of the chlorophyll a/b-binding proteins: cDNA's encoding Type I, II and III LHC I polypeptides from the gymnosperm Scots pine. Mol Gen Genet 229: 67–76 (1991).

    Google Scholar 

  19. Jansson S, Pichersky E, Bassi R, Green BR, Ikeuchi M, Melis A, Simpson DJ, Spangfort M, Staehelin LA, Thornber JP: A nomenclature for the genes encoding the chlorophyll a/b-binding proteins of higher plants. Plant Mol Biol Rep 10: 242–253 (1992).

    Google Scholar 

  20. Jefferson RA, Kavanagh TA, Bevan MW: GUS fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6: 3901–3907 (1987).

    Google Scholar 

  21. Jensen PE, Kristensen M, Hoff T, Lehmbeck J, Stummann BM, Hennigsen KW: Identification of a single-copy gene encoding a Type I chlorophyll a/b-binding polypeptide of photosystem I in Arabidopsis thaliana. Physiol Plant 84: 561–567 (1992).

    Google Scholar 

  22. Joshi CP: An inspection of the domain between putative TATA box and translation start site in 79 plant genes. Nucl Acids Res 15: 6643–6653 (1987).

    Google Scholar 

  23. Ikeuchi M, Hirano A, Inoue Y: Correspondence of apoproteins of light-harvesting chlorophyll a/b complexes associated with photosystem I to cab genes: evidence for a novel type IV apoprotein. Plant Cell Physiol 32: 103–112 (1991).

    Google Scholar 

  24. LÜtcke HA, Chow KC, Mickel FS, Moss KA, Kern HF, Scheele GA: Selection of AUG initiation codons differs in plants and animals. EMBO J 6: 43–48 (1987).

    Google Scholar 

  25. Meagher RB, Berry-Lowe S, Rice K: Molecular evolution of the small subunit of ribulose bisphosphate carboxylase: nucleotide substitution and gene conversion. Genetics 123: 845–863 (1989).

    Google Scholar 

  26. Meyer H, Thienel U, Piechulla B: Molecular characterization of the diurnal/circadian expression of the chlorophyll a/b binding proteins in leaves of tomato and other dicotyledonous and monocotyledonous plant species Planta 180: 5–15 (1989).

    Google Scholar 

  27. Mural RJ, Einstein JR, Guan X, Mann RC, Uberbacher EC. An artificial intelligence program to DNA sequence feature recognition. Trends Biotechnol 10: 66–69 (1992).

    Google Scholar 

  28. Nantel AM, Lafleur F, Boivin R, Baszczynski CL, Bellemare G: Promoter for a Brassica napus ribulose phosphate carboxylase/oxygenase small subunit gene binds multiple nuclear factors and contains a negative-strand open reading frame encoding a putative membrane protein. Plant Mol Biol 16: 955–966 (1991).

    Google Scholar 

  29. Nap JP, Dirkse WG, Louwerse J, Onstenk J, Visser R, Loonen A, Heidekamp F, Stiekema WJ. Analysis of the region inbetween two closely linked patatin genes: class II promoter activity in tuber, root and leaf. Plant Mol Biol 20: 683–694 (1992).

    Google Scholar 

  30. Pichersky E, Hoffman NE, Bernatzky R, Piechulla B, Tanksley SD, Cashmore AR: Molecular characterization and genetic mapping of DNA sequences encoding the Type I chlorophyll a/b-binding polypeptide of photosystem I in Lycopersicon esculentum (tomato). Plant Mol Biol 9: 205–216 (1987).

    Google Scholar 

  31. Pichersky E, Tanksley SD, Piechulla B, Stayton MM, Dunsmuir P: Nucleotide sequence and chromosomal location of Cab-7, the tomato gene encoding the Type II chlorophyll a/b-binding polypeptide of Photosystem I. Plant Mol Biol 11: 69–71 (1988).

    Google Scholar 

  32. Pichersky E, Brock TG, Nguyen D, Hoffman NE, Piechulla B, Tanksley SD, Cashmore AR: A new member of the CAB gene family: structure, expression and chromosomal location of Cab-8, the tomato gene encoding the Type III chlorophyll a/b-binding polypeptide of photosystem I. Plant Mol Biol 12: 257–270 (1989).

    Google Scholar 

  33. Rapp JC, Mullet JE: Chloroplast transcription is required to express the nuclear genes rbcS and cab. Plastid DNA copy number is regulated independently. Plant Mol Biol 17: 813–823 (1991).

    Google Scholar 

  34. Schindler U, Cashmore AR: Photoregulated gene expression may involve ubiquitous DNA binding proteins. EMBO J 9: 3415–3427 (1990).

    Google Scholar 

  35. Schwartz E, Shen D, Aebersold R, McGrath JM, Pichersky E, Green BR: Nucleotide sequence and chromosomal location of Cab11 and Cab12, the genes for the fourth polypeptide of the photosystem I light-harvesting antenna (LHCI). FEBS Lett 280: 229–234 (1991).

    Google Scholar 

  36. Sheen J: Metabolic repression of transcription in higher plants. Plant Cell 2: 1027–1038 (1990).

    Google Scholar 

  37. Simpson J, vanMontagu M, Herrera-Estrella L: Photosynthesis-associated gene families: differences in response to tissue-specific and environmental factors. Science 233: 34–38 (1986).

    Google Scholar 

  38. Smeekens S, vanBinsbergen J, Weisbeek P: The plant ferredoxin precursor: nucleotide sequence of a full length cDNA clone. Nucl Acids Res 13: 3179–3194 (1985).

    Google Scholar 

  39. Smeekens S, deGroot M, vanBinsbergen J, Weisbeek P: Sequence of the precursor of the chloroplast lumen protein plastocyanin. Nature 317: 456–458 (1985).

    Google Scholar 

  40. Sprent P. Applied Nonparametric Statistical Methods. Chapman and Hall, London (1988).

    Google Scholar 

  41. Stayton MM, Brosio P, Dunsmuir P: Characterization of a full length petunia cDNA encoding a polypeptide of the light-harvesting complex associated with photosystem I. Plant Mol Biol 10: 127–137 (1987).

    Google Scholar 

  42. vanSpanje M, Dirkse WG, Nap JP, Stiekema WJ: Isolation and analysis of cDNA encoding the 33 kDa precursor protein of the oxygen-evolving complex of potato. Plant Mol Biol 17: 157–160 (1991).

    Google Scholar 

  43. vonHeijne G, Steppuhn J, Herrmann R: Domain structure of mitochondrial and chloroplast targeting peptides. Eur J Biochem 180: 535–545 (1989).

    Google Scholar 

  44. Zhang H, Hanley S, Goodman HM: Isolation, characterization, and chromosomal location of a new cab gene from Arabidonsis thaliana. Plant Physiol 96: 1387–1388 (1991).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nap, JP., van Spanje, M., Dirkse, W.G. et al. Activity of the promoter of the Lhca3.St.1 gene, encoding the potato apoprotein 2 of the light-harvesting complex of Photosystem I, in transgenic potato and tobacco plants. Plant Mol Biol 23, 605–612 (1993). https://doi.org/10.1007/BF00019307

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00019307

Key words

Navigation