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The maize GapC4 promoter confers anaerobic reporter gene expression and shows homology to the maize anthocyanin regulatory locus C1

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Abstract

The cytosolic glyceraldehyde-3-phosphate dehydrogenase (GapC) gene family of maize is differentially expressed in response to anaerobic stress. While GapC1 and GapC2 are downregulated, GapC3 and GapC4 are anaerobically induced. We have sequenced and analyzed a 3073 bp promoter fragment of GapC4. The promoter confers anaerobic induction of a reporter gene construct in a transient gene expression system in maize. Deletion analysis of the GapC4 promoter revealed a 270 bp long DNA region required for anaerobic induction. This region contains sequence motifs resembling the cis-acting sequences of the anaerobically induced maize Adh1 and Adh2 genes. Furthermore, the 3073 bp GapC4 promoter fragment displays homology to long terminal repeats of maize retrotransposons and to the 3′ region of the maize anthocyanin regulatory locus C1.

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References

  1. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ: Basic local alignment search tool. J Mol Biol 215: 403–410 (1990).

    Google Scholar 

  2. Bradford MM: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 7: 248–254 (1976).

    Google Scholar 

  3. Callis J, Fromm M, Walbot V: Introns increase gene expression in cultured maize cells. Genes Devel 1: 1183–1200 (1987).

    Google Scholar 

  4. Cerff R: The chimeric nature of nuclear genomes and the antiquity of introns as demonstrated by the GAPDH gene system. In: M.Go (ed) Proceedings of the 20th Tanguchi International Symposium ‘Tracing biological evolution in protein and gene structures’, Nagoya, Japan, Elsevier Science, Amsterdam, Netherlands, in press (1995).

    Google Scholar 

  5. de Wet JR, Wood KV, DeLuca M, Helinski DR, Subramani S: Firefly luciferase gene: structure and expression in mammalian cells. Mol Cell Biol 7: 725–737 (1987).

    Google Scholar 

  6. Ferl RJ: ARF-B2: a protein complex that specifically binds to part of the anaerobic response element of maize Adh1. Plant Physiol 93: 1094–1101 (1990).

    Google Scholar 

  7. Hu W, Das O, Messing J: Zeon-1, a member of a new maize retrotransposon family. Mol Gen Genet 248: 471–480 (1995).

    Google Scholar 

  8. 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 

  9. Kersanach R, Brinkmann H, Liaud M-F, Zhang D-X, Martin WF, Cerff R: Five identical intron positions in ancient duplicated genes of eubacterial origin. Nature 367: 387–389 (1994).

    Google Scholar 

  10. Klein TM, Gradziel T, Fromm ME, Sanford JC: Factors influencing gene delivery into Zea mays cells by high-velocity microprojectiles. Bio/technology 6: 559–563 (1988).

    Google Scholar 

  11. Kriz AL, Boston RS, Larkins BA: Structural and transcriptional analysis of DNA sequences flanking genes that encode 19 kilodalton zeins. Mol Gen Genet 207: 90–98 (1987).

    Google Scholar 

  12. Maas C, Laufs J, Grant S, Korfhage C, Werr W: The combination of a novel stimulatory element in the first exon of the maize ShrunkenI gene with the following intron 1 enhances reporter gene expression up to 1000-fold. Plant Mol Biol 16: 199–207 (1991).

    Google Scholar 

  13. Martinez P, Martin W, Cerff R: Structure, evolution and anaerobic regulation of a nuclear gene encoding cytosolic glyceraldehyde-3-phosphate dehydrogenase from maize. J Mol Biol 208: 551–565 (1989).

    Google Scholar 

  14. Murashige T, Skoog F: A revised medium for rapid growth and bioassay with tobacco tissue cultures. Physiol Plant 15: 473–497 (1962).

    Google Scholar 

  15. Olive MR, Peacock WJ, Dennis ES: The anaerobic responsive element contains two GC-rich sequences essential for binding a nuclear protein and hypoxic activation of the maize Adh1 promoter. Nucl Acids Res 19: 7053–7060 (1991).

    Google Scholar 

  16. Paul A-L, Ferl RJ: In vivo footprinting reveals unique cis-elements and different modes of hypoxic induction in maize Adh1 and Adh2. Plant Cell 3: 159–168 (1991).

    Google Scholar 

  17. Paz-Ares J, Ghosal D, Wienand U, Peterson PA, Saedler H: The regulatory c1 locus of Zea mays encodes a protein with homology to myb proto-oncogene products and with structural similarities to transcriptional activators. EMBO J 6: 3553–3558 (1987).

    Google Scholar 

  18. Perata P, Alpi A: Plant responses to anaerobiosis. Plant Sci 93: 1–17 (1993).

    Google Scholar 

  19. Reina M, Ponte I, Guillén P, Boronat A, Palau J: Sequence analysis of a genomic clone encoding a Zc2 protein from Zea mays W64 A. Nucl Acids Res 18: 6426 (1990).

    Google Scholar 

  20. Russell DA, Sachs MM: Differential expression and sequence analysis of the maize glyceraldehyde-3-phosphate dehydrogenase gene family. Plant Cell 1: 793–803 (1989).

    Google Scholar 

  21. Russell DA, Sachs MM: Protein synthesis in maize during anaerobic and heat stress. Plant Physiol 99: 615–620 (1992).

    Google Scholar 

  22. Sachs MM, Freeling M, Okimoto R: The anaerobic proteins of maize. Cell 20: 761–767 (1980).

    Google Scholar 

  23. Sanford JC: The biolistic process. Trends Biotechnol 6: 299–302 (1988).

    Google Scholar 

  24. Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (1989).

    Google Scholar 

  25. Scheffler B, Franken P, Schrell A, Saedler H, Wienand U: Molecular analysis of C1 alleles in Zea mays defines regions involved in the expression of this regulatory gene. Mol Gen Genet 242: 40–48 (1994).

    Google Scholar 

  26. Schledzewski K, Mendel RR: Quantitative transient gene expression: comparison of the promoters for maize polyubiquitin1, rice actin1, maize derived Emu and CaMV 35S in cells of barley, maize and tobacco. Transgen Res 3: 249–255 (1994).

    Google Scholar 

  27. Shepherd NS, Schwarz-Sommer Z, Blumberg vel Spalve J, Gupta M, Wienand U, Saedler H: Similarity of the Cin1 repetitive family of Zea mays to eukaryotic transposable elements. Nature 307: 185–187 (1984).

    Google Scholar 

  28. Vain P, McCullen MD, Finer JJ: Osmotic treatment enhances particle bombardment-mediated transient and stable transformation of maize. Plant Cell Rep 12: 84–88 (1993).

    Google Scholar 

  29. Walker JC, Howard EA, Dennis ES, Peacock WJ: DNA sequences required for anaerobic expression of the maize alcohol dehydrogenase 1 gene. Proc Natl Acad Sci USA 84: 6624–6628 (1987).

    Google Scholar 

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Köhler, U., Liaud, MF., Mendel, R.R. et al. The maize GapC4 promoter confers anaerobic reporter gene expression and shows homology to the maize anthocyanin regulatory locus C1 . Plant Mol Biol 29, 1293–1298 (1995). https://doi.org/10.1007/BF00020469

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  • DOI: https://doi.org/10.1007/BF00020469

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