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. 1989 Jul;1(7):715–725. doi: 10.1105/tpc.1.7.715

Salt stress leads to differential expression of two isogenes of phosphoenolpyruvate carboxylase during Crassulacean acid metabolism induction in the common ice plant.

J C Cushman 1, G Meyer 1, C B Michalowski 1, J M Schmitt 1, H J Bohnert 1
PMCID: PMC159808  PMID: 2535520

Abstract

The common ice plant is a facultative halophyte in which Crassulacean acid metabolism, a metabolic adaptation to arid environments, can be induced by irrigating plants with high levels of NaCl or by drought. This stress-induced metabolic transition is accompanied by up to a 50-fold increase in the activity of phosphoenolpyruvate carboxylase (PEPCase). To analyze the molecular basis of this plant response to water stress, we have isolated and characterized two members of the PEPCase gene family from the common ice plant. The PEPCase isogenes, designated Ppc1 and Ppc2, have conserved intron-exon organizations, are 76.4% identical at the nucleotide sequence level within exons, and encode predicted polypeptides with 83% amino acid identity. Steady-state levels of mRNAs from the two genes differ dramatically when plants are salt-stressed. Transcripts of Ppc1 increase about 30-fold in leaves within 5 days of salt stress. In contrast, steady-state levels of Ppc2 transcripts decrease slightly in leaf tissue over the same stress period. Steady-state levels of transcripts of both genes decrease in roots over 5 days of salt stress. We have used in vitro transcription assays with nuclei isolated from leaves to demonstrate that the increased expression of Ppc1 caused by water stress occurs in part at the transcriptional level.

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Selected References

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  1. Benton W. D., Davis R. W. Screening lambdagt recombinant clones by hybridization to single plaques in situ. Science. 1977 Apr 8;196(4286):180–182. doi: 10.1126/science.322279. [DOI] [PubMed] [Google Scholar]
  2. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Hagen G., Guilfoyle T. J. Rapid induction of selective transcription by auxins. Mol Cell Biol. 1985 Jun;5(6):1197–1203. doi: 10.1128/mcb.5.6.1197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Harpster M. H., Taylor W. C. Maize phosphoenolpyruvate carboxylase. Cloning and characterization of mRNAs encoding isozymic forms. J Biol Chem. 1986 May 5;261(13):6132–6136. [PubMed] [Google Scholar]
  5. Hudspeth R. L., Glackin C. A., Bonner J., Grula J. W. Genomic and cDNA clones for maize phosphoenolpyruvate carboxylase and pyruvate,orthophosphate dikinase: Expression of different gene-family members in leaves and roots. Proc Natl Acad Sci U S A. 1986 May;83(9):2884–2888. doi: 10.1073/pnas.83.9.2884. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Höfner R., Vazquez-Moreno L., Winter K., Bohnert H. J., Schmitt J. M. Induction of Crassulacean Acid Metabolism in Mesembryanthemum crystallinum by High Salinity: Mass Increase and de Novo Synthesis of PEP-Carboxylase. Plant Physiol. 1987 Apr;83(4):915–919. doi: 10.1104/pp.83.4.915. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lipman D. J., Pearson W. R. Rapid and sensitive protein similarity searches. Science. 1985 Mar 22;227(4693):1435–1441. doi: 10.1126/science.2983426. [DOI] [PubMed] [Google Scholar]
  8. Michalowski C. B., Olson S. W., Piepenbrock M., Schmitt J. M., Bohnert H. J. Time Course of mRNA Induction Elicited by Salt Stress in the Common Ice Plant (Mesembryanthemum crystallinum). Plant Physiol. 1989 Mar;89(3):811–816. doi: 10.1104/pp.89.3.811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Michalowski C. B., Schmitt J. M., Bohnert H. J. Expression during Salt Stress and Nucleotide Sequence of cDNA for Ferredoxin-NADP Reductase from Mesembryanthemum crystallinum. Plant Physiol. 1989 Mar;89(3):817–822. doi: 10.1104/pp.89.3.817. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Mount S. M. A catalogue of splice junction sequences. Nucleic Acids Res. 1982 Jan 22;10(2):459–472. doi: 10.1093/nar/10.2.459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ostrem J. A., Olson S. W., Schmitt J. M., Bohnert H. J. Salt Stress Increases the Level of Translatable mRNA for Phosphoenolpyruvate Carboxylase in Mesembryanthemum crystallinum. Plant Physiol. 1987 Aug;84(4):1270–1275. doi: 10.1104/pp.84.4.1270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Rickers J., Cushman J. C., Michalowski C. B., Schmitt J. M., Bohnert H. J. Expression of the CAM-form of phospho(enol)pyruvate carboxylase and nucleotide sequence of a full length cDNA from Mesembryanthemum crystallinum. Mol Gen Genet. 1989 Feb;215(3):447–454. doi: 10.1007/BF00427042. [DOI] [PubMed] [Google Scholar]
  13. Sipes D. L., Ting I. P. Crassulacean Acid Metabolism and Crassulacean Acid Metabolism Modifications in Peperomia camptotricha. Plant Physiol. 1985 Jan;77(1):59–63. doi: 10.1104/pp.77.1.59. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Tabor S., Richardson C. C. DNA sequence analysis with a modified bacteriophage T7 DNA polymerase. Proc Natl Acad Sci U S A. 1987 Jul;84(14):4767–4771. doi: 10.1073/pnas.84.14.4767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ting I. P., Hanscom Z. Induction of Acid Metabolism in Portulacaria afra. Plant Physiol. 1977 Mar;59(3):511–514. doi: 10.1104/pp.59.3.511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ting I. P., Osmond C. B. Multiple forms of plant phosphoenolpyruvate carboxylase associated with different metabolic pathways. Plant Physiol. 1973 Mar;51(3):448–453. doi: 10.1104/pp.51.3.448. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Vernon D. M., Ostrem J. A., Schmitt J. M., Bohnert H. J. PEPCase Transcript Levels in Mesembryanthemum crystallinum Decline Rapidly upon Relief from Salt Stress. Plant Physiol. 1988 Apr;86(4):1002–1004. doi: 10.1104/pp.86.4.1002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Vieira J., Messing J. Production of single-stranded plasmid DNA. Methods Enzymol. 1987;153:3–11. doi: 10.1016/0076-6879(87)53044-0. [DOI] [PubMed] [Google Scholar]
  19. Yanagisawa S., Izui K., Yamaguchi Y., Shigesada K., Katsuki H. Further analysis of cDNA clones for maize phosphoenolpyruvate carboxylase involved in C4 photosynthesis. Nucleotide sequence of entire open reading frame and evidence for polyadenylation of mRNA at multiple sites in vivo. FEBS Lett. 1988 Feb 29;229(1):107–110. doi: 10.1016/0014-5793(88)80807-x. [DOI] [PubMed] [Google Scholar]

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