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. 1987;209(3):552–562. doi: 10.1007/BF00331162

Cloning of DNA fragments complementary to tobacco nitrate reductase mRNA and encoding epitopes common to the nitrate reductases from higher plants

Roger Calza 1, Eric Huttner 1, Michel Vincentz 1, Pierre Rouzé 1, Fabienne Galangau 1, Hervé Vaucheret 1, Isabelle Chérel 1, Christian Meyer 1, Jocelyne Kronenberger 1, Michel Caboche 1,
PMCID: PMC7087718  PMID: 17193712

Summary

Messenger RNAs encoding the nitrate reductase apoenzyme from tobacco can be translated in a cell-free system. Poly(A)+ mRNA fractions from the 23-32 S area of a sucrose gradient were used to build a cDNA library in the expression vector λgt11 with an efficiency of cloning of approximately 104 recombinants/ng mRNA. Recombinant clones were screened with a rabbit polyclonal antibody directed against the corn nitrate reductase, which cross reacts specifically with the nitrate reductases from dicotyledons. Among 240000 recombinant plaques, eight clones were isolated containing inserts of sizes ranging from 1.6 kb to 2.1 kb and sharing sequence homologies. Seven of these clones contained a common internal 1.6 kb EcoRI fragment. The identity of these clones was confirmed as follows. A fusion protein of 170 kDa inducible by IPTG and recognized by the rabbit nitrate reductase antibody was expressed by a lysogen derived from one of the recombinants. The antibodies binding the fused protein were eluted and shown to be inhibitory to the catalytic activity of tobacco nitrate reductase. Two monoclonal antibodies directed against nitrate reductase were also able to bind the hybrid protein. The 1.6 kb EcoRI fragment was sequenced by the method of Sanger. The open reading frame corresponding to a translational fusion with the β-galactosidase coding sequence of the vector shared strong homology at the amino acid level with the heme-binding domain of proteins of the cytochrome b5 superfamily and with human erythrocyte cytochrome b5 reductase. When the 1.6 kb EcoRI fragment was used as a probe for Northern blot experiments a signal corresponding to a 3.5 kb RNA was detected in tobacco and in Nicotiana plumbaginifolia mRNA preparations but no cross-hybridization with corn mRNAs was detected. The probe hybridized with low copy number sequences in genomic blots of tobacco DNA.

Key words: Nitrate reductase, cDNA expression cloning, Tobacco, Sequence, Cytochrome b5

Abbreviations

DMSO

dimethylsulfoxide

ELISA

enzyme-linked immunosorbent assay

IPTG

isopropyl β-D-thiogalactopyranoside

PMSF

phenylmethylsulfonyl fluoride

XGal

5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside

References

  1. Bantle JA, Maxwell IH, Hahn WE. Specificity of oligo (dT)-cellulose chromatography in the isolation of polyadenylated RNA. Anal Biochem. 1978;70:75–85. doi: 10.1016/0003-2697(76)90549-2. [DOI] [PubMed] [Google Scholar]
  2. Campbell WH, Redinbaugh MG. Ferric-citrate reductase activity of nitrate reductase and its role in iron assimilation by plants. J Plant Nutr. 1984;7:799–806. [Google Scholar]
  3. Campbell WH, Wray J. Purification of barley nitrate reductase and demonstration of nicked subunits. Phytochemistry. 1983;22:2375–2382. [Google Scholar]
  4. Chérel I, Grosclaude J, Rouzé P. Monoclonal antibodies identify multiple epitopes on maize leaf nitrate reductase. Biochem Biophys Res Commun. 1985;129:686–693. doi: 10.1016/0006-291X(85)91946-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chérel I, Marion-Poll A, Meyer C, Rouzé P. Immunological comparisons of nitrate reductases of different plant species using monoclonal antibodies. Plant Physiol. 1986;81:376–378. doi: 10.1104/pp.81.2.376. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chirgwin JM, Przybyla AE, MacDonald RJ, Rutter WJ. Isolation of biologically active RNA from sources enriched in ribonucleases. Biochemistry. 1979;18:5294–5299. doi: 10.1021/bi00591a005. [DOI] [PubMed] [Google Scholar]
  7. Commère B, Chérel I, Kronenberger J, Galangau F, Caboche M. In vitro translation of nitrate reductase messenger RNA from maize and tobacco and detection with an antibody directed against the enzyme of maize. Plant Sci. 1986;44:191–203. [Google Scholar]
  8. Dellaporta SL, Wood J, Hicks JB. A plant DNA miniprep: version II. Plant Mol Biol Reporter. 1983;1:19–21. [Google Scholar]
  9. Dente L, Sollazzo M, Baldari C, Cesareni G, Cortese R. The pEMBL family of single-stranded vectors. In: Glover DM, editor. DNA cloning: A practical approach. Oxford, Washington DC: IRL Press; 1985. pp. 101–107. [Google Scholar]
  10. Deshayes A, Herrera Estrella L, Caboche M. Liposome-mediated transformation of tobacco mesophyll protoplasts by an Escherichia coli plasmid. EMBO J. 1985;4:2731–2737. doi: 10.1002/j.1460-2075.1985.tb03996.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gabard J, Marion-Poll A, Chérel I, Meyer C, Muller AJ, Caboche M. Isolation and characterization of Nicotiana plumbaginifolia nitrate-reductase deficient mutants: genetic and biochemical analysis of the nia complementation group. Mol Gen Genet. 1987;209:596–606. doi: 10.1007/BF00331169. [DOI] [PubMed] [Google Scholar]
  12. Gerlach WL, Bedbrook J. Cloning and characterization of ribosomal RNA genes from wheat and barley. Nucleic Acids Res. 1979;7:1869–1885. doi: 10.1093/nar/7.7.1869. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gubler U, Hoffmann BJ. A simple and very efficient method for generating cDNA libraries. Gene. 1983;25:263–269. doi: 10.1016/0378-1119(83)90230-5. [DOI] [PubMed] [Google Scholar]
  14. Guiard B, Lederer F. The “cytochrome b5 fold”: structure of a novel protein superfamily. J Mol Biol. 1979;135:639–650. doi: 10.1016/0022-2836(79)90169-4. [DOI] [PubMed] [Google Scholar]
  15. Guiard B, Lederer F. Amino acid sequence of the b5-like heme-binding domain from chicken sulfite oxidase. Eur J Biochem. 1979;100:441–453. doi: 10.1111/j.1432-1033.1979.tb04187.x. [DOI] [PubMed] [Google Scholar]
  16. Henikoff S. Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. Gene. 1984;28:351–359. doi: 10.1016/0378-1119(84)90153-7. [DOI] [PubMed] [Google Scholar]
  17. Hewitt SJ. Assimilatory nitrate and nitrate reduction. Annu Rev Plant Physiol. 1975;26:73–100. [Google Scholar]
  18. Howard WD, Solomonson LP. Quaternary structure of assimilatory NADH: nitrate reductase from Chlorella. J Biol Chem. 1982;257:10243–10250. [PubMed] [Google Scholar]
  19. Huynh TV, Young RA, Davis RW. Construction and screening cDNA libraries in lambda gt10 and lambda gt11. In: Glover DM, editor. DNA cloning: A practical approach. Oxford: IRL Press; 1985. pp. 49–78. [Google Scholar]
  20. Kleinhofs A, Warner RL, Narayanan KR. Current progress towards an understanding of the genetics and molecular biology of nitrate reductase in higher plants. Oxford Surveys of Plant Mol Cell Biol. 1985;2:91–121. [Google Scholar]
  21. Lapeyre B (1985) Isolement et caractérisation d'ADNc codant pour une protéine nucléolaire de 100 kDa. PhD Thesis, Toulouse University
  22. Lê KHD, Lederer F. On the presence of a heme-binding domain homologous to cytochrome b5 in Neurospora crassa assimilatory nitrate reductase. EMBO J. 1983;2:1909–1914. doi: 10.1002/j.1460-2075.1983.tb01678.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Lederer F, Ghrir R, Guiard B, Cortial S, Ito A. Two homologous cytochrome b5 in a single cell. Eur J Biochem. 1983;132:95–102. doi: 10.1111/j.1432-1033.1983.tb07330.x. [DOI] [PubMed] [Google Scholar]
  24. Lederer F, Cortial S, Becam AM, Haumont PY, Perez L. Complete amino acid sequence of flavocytochrome b2 from baker's yeast. Eur J Biochem. 1985;152:419–423. doi: 10.1111/j.1432-1033.1985.tb09213.x. [DOI] [PubMed] [Google Scholar]
  25. Maniatis T, Fritsch EF, Sambrook J. Molecular cloning: A laboratory manual. Cold Spring Harbor, New York: Cold Spring Harbor Laboratory; 1982. [Google Scholar]
  26. Mathews FS, Levine M, Argos P. The structure of calf liver cytochrome b5 at 2.8 Å resolution. Nature New Biol. 1971;233:15–16. doi: 10.1038/newbio233015a0. [DOI] [PubMed] [Google Scholar]
  27. Miller JH. Experiments in Molecular Genetics. Cold Spring Harbor, New York: Cold Spring Harbor Laboratory; 1972. [Google Scholar]
  28. Messing J. New vectors for cloning. Methods Enzymol. 1983;101:20–78. doi: 10.1016/0076-6879(83)01005-8. [DOI] [PubMed] [Google Scholar]
  29. Müller AJ. Genetic analysis of nitrate reductase-deficient tobacco plants regenerated from mutant cells. Evidence for duplicate structural genes. Mol Gen Genet. 1983;192:275–281. [Google Scholar]
  30. Nobrega FG, Ozols J. Amino acid sequences of tryptic peptides of cytochromes b5 from microsomes of human, monkey, porcine and chicken liver. J Biol Chem. 1971;246:1706–1717. [PubMed] [Google Scholar]
  31. Ozols J, Heinemann FS. Chemical structure of rat liver cytochrome b5. Isolation of peptides by high-pressure liquid chromatography. Biochim Biophys Acta. 1982;704:163–173. doi: 10.1016/0167-4838(82)90143-1. [DOI] [PubMed] [Google Scholar]
  32. Ozols J, Strittmatter P. Correction of the amino acid sequence of calf liver microsomal cytochrome b5. J Biol Chem. 1969;244:6617–6618. [PubMed] [Google Scholar]
  33. Ozols J, Gerard C, Nobrega F. Proteolytic cleavage of horse liver cytochrome b5. Primary structure of the heme-containing moiety. J Biol Chem. 1976;251:6767–6774. [PubMed] [Google Scholar]
  34. Rasul Chaudhry G, MacGregor CH. Escherichia coli nitrate reductase subunit A: Its role on the catalytic site and evidence for its modification. J Bacteriol. 1983;154:387–394. doi: 10.1128/jb.154.1.387-394.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Redinbaugh MG, Campbell WH. Quaternary structure and composition of squash NADH nitrate reductase. J Biol Chem. 1985;260:3380–3385. [PubMed] [Google Scholar]
  36. Riva M (1985) Deux approches nouvelles à l'étude des ARN polymérases de Saccharomyces cerevisae: la formation d'enzymes hybrides et l'isolement des gènes de structure. PhD Thesis, Université Paris VI
  37. Sanger F, Nicklen S, Coulson AR. DNA sequencing with chain termination inhibitors. Proc Natl Acad Sci USA. 1977;74:5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Thomas SP. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci USA. 1980;77:5201–5205. doi: 10.1073/pnas.77.9.5201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Tsugita A, Kobayashi M, Tani S, Kyo S, Rashid MA, Yoshida Y, Kajihara T, Hagihara B. Comparative study of the primary structures of cytochrome b5 from four species. Proc Natl Acad Sci USA. 1970;67:442–447. doi: 10.1073/pnas.67.1.442. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Vieira J, Messing J. the pUC plasmid, an M13 mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers. Gene. 1982;19:259–268. doi: 10.1016/0378-1119(82)90015-4. [DOI] [PubMed] [Google Scholar]
  41. Xia Z, Shamala N, Bethge PH, Lim LW, Bellamy HD, Xuong NH, Lederer F, Mathews FS. Three-dimensional structure of flavocytochrome b2 from baker's yeast at 3.0-A resolution. Biochemistry. 1987;84:2629–2633. doi: 10.1073/pnas.84.9.2629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Yabisui T, Miyata T, Iwanaga S, Tamura M, Yoshida S, Takeshita M, Nakajima H. Amino acid sequence of NADH-cytochrome b5 reductase of human erythrocytes. J Biochem. 1984;96:579–582. doi: 10.1093/oxfordjournals.jbchem.a134871. [DOI] [PubMed] [Google Scholar]
  43. Yanish-Perron C, Viera J, Messing J. Improved M13 phage cloning vectors and host strains: Nucleotide sequences of the M13 mp18 and pUC19 vectors. Gene. 1985;33:103–119. doi: 10.1016/0378-1119(85)90120-9. [DOI] [PubMed] [Google Scholar]
  44. Young RA, Davis RW. Efficient isolation of genes by using antibody probes. Proc Natl Acad Sci USA. 1983;80:1194–1198. doi: 10.1073/pnas.80.5.1194. [DOI] [PMC free article] [PubMed] [Google Scholar]

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