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. 1993 Apr;5(4):419–432. doi: 10.1105/tpc.5.4.419

Interorgan regulation of ethylene biosynthetic genes by pollination.

S D O'Neill 1, J A Nadeau 1, X S Zhang 1, A Q Bui 1, A H Halevy 1
PMCID: PMC160281  PMID: 8318838

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Selected References

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  1. Anderson J. D., Mattoo A. K., Lieberman M. Induction of ethylene biosynthesis in tobacco leaf discs by cell wall disesting enzymes. Biochem Biophys Res Commun. 1982 Jul 30;107(2):588–596. doi: 10.1016/0006-291x(82)91532-7. [DOI] [PubMed] [Google Scholar]
  2. Aviv H., Leder P. Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1408–1412. doi: 10.1073/pnas.69.6.1408. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bradford K. J., Yang S. F. Xylem Transport of 1-Aminocyclopropane-1-carboxylic Acid, an Ethylene Precursor, in Waterlogged Tomato Plants. Plant Physiol. 1980 Feb;65(2):322–326. doi: 10.1104/pp.65.2.322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Burg S. P., Burg E. A. Molecular requirements for the biological activity of ethylene. Plant Physiol. 1967 Jan;42(1):144–152. doi: 10.1104/pp.42.1.144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cathala G., Savouret J. F., Mendez B., West B. L., Karin M., Martial J. A., Baxter J. D. A method for isolation of intact, translationally active ribonucleic acid. DNA. 1983;2(4):329–335. doi: 10.1089/dna.1983.2.329. [DOI] [PubMed] [Google Scholar]
  6. Dong J. G., Olson D., Silverstone A., Yang S. F. Sequence of a cDNA coding for a 1-aminocyclopropane-1-carboxylate oxidase homolog from apple fruit. Plant Physiol. 1992 Apr;98(4):1530–1531. doi: 10.1104/pp.98.4.1530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
  8. Flowers J. V., Booraem C., Miller T. E., Iverson A. E., Copeland J., Furtado K. Comparison of the results of a standardized AIDS prevention program in three geographic locations. AIDS Educ Prev. 1991 Fall;3(3):189–196. [PubMed] [Google Scholar]
  9. Gilissen L. J., Hoekstra F. A. Pollination-Induced Corolla Wilting in Petunia hybrida Rapid Transfer through the Style of a Wilting-Inducing Substance. Plant Physiol. 1984 Jun;75(2):496–498. doi: 10.1104/pp.75.2.496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Haring V., Gray J. E., McClure B. A., Anderson M. A., Clarke A. E. Self-incompatibility: a self-recognition system in plants. Science. 1990 Nov 16;250(4983):937–941. doi: 10.1126/science.2237440. [DOI] [PubMed] [Google Scholar]
  11. Hoekstra F. A., Weges R. Lack of Control by Early Pistillate Ethylene of the Accelerated Wilting of Petunia hybrida Flowers. Plant Physiol. 1986 Feb;80(2):403–408. doi: 10.1104/pp.80.2.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Huang P. L., Parks J. E., Rottmann W. H., Theologis A. Two genes encoding 1-aminocyclopropane-1-carboxylate synthase in zucchini (Cucurbita pepo) are clustered and similar but differentially regulated. Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):7021–7025. doi: 10.1073/pnas.88.16.7021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. McMurchie E. J., McGlasson W. B., Eaks I. L. Treatment of fruit with propylene gives information about the biogenesis of ethylene. Nature. 1972 May 26;237(5352):235–236. doi: 10.1038/237235a0. [DOI] [PubMed] [Google Scholar]
  14. Nasrallah J. B., Yu S. M., Nasrallah M. E. Self-incompatibility genes of Brassica oleracea: Expression, isolation, and structure. Proc Natl Acad Sci U S A. 1988 Aug;85(15):5551–5555. doi: 10.1073/pnas.85.15.5551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Nevins J. R., Wilson M. C. Regulation of adenovirus-2 gene expression at the level of transcriptional termination and RNA processing. Nature. 1981 Mar 12;290(5802):113–118. doi: 10.1038/290113a0. [DOI] [PubMed] [Google Scholar]
  16. Oeller P. W., Lu M. W., Taylor L. P., Pike D. A., Theologis A. Reversible inhibition of tomato fruit senescence by antisense RNA. Science. 1991 Oct 18;254(5030):437–439. doi: 10.1126/science.1925603. [DOI] [PubMed] [Google Scholar]
  17. Olson D. C., White J. A., Edelman L., Harkins R. N., Kende H. Differential expression of two genes for 1-aminocyclopropane-1-carboxylate synthase in tomato fruits. Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5340–5344. doi: 10.1073/pnas.88.12.5340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Park K. Y., Drory A., Woodson W. R. Molecular cloning of an 1-aminocyclopropane-1-carboxylate synthase from senescing carnation flower petals. Plant Mol Biol. 1992 Jan;18(2):377–386. doi: 10.1007/BF00034964. [DOI] [PubMed] [Google Scholar]
  19. Pearce G., Strydom D., Johnson S., Ryan C. A. A polypeptide from tomato leaves induces wound-inducible proteinase inhibitor proteins. Science. 1991 Aug 23;253(5022):895–897. doi: 10.1126/science.253.5022.895. [DOI] [PubMed] [Google Scholar]
  20. Sato T., Oeller P. W., Theologis A. The 1-aminocyclopropane-1-carboxylate synthase of Cucurbita. Purification, properties, expression in Escherichia coli, and primary structure determination by DNA sequence analysis. J Biol Chem. 1991 Feb 25;266(6):3752–3759. [PubMed] [Google Scholar]
  21. Thomas P. S. Hybridization of denatured RNA transferred or dotted nitrocellulose paper. Methods Enzymol. 1983;100:255–266. doi: 10.1016/0076-6879(83)00060-9. [DOI] [PubMed] [Google Scholar]
  22. Van der Straeten D., Van Wiemeersch L., Goodman H. M., Van Montagu M. Cloning and sequence of two different cDNAs encoding 1-aminocyclopropane-1-carboxylate synthase in tomato. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4859–4863. doi: 10.1073/pnas.87.12.4859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Wahl G. M., Berger S. L., Kimmel A. R. Molecular hybridization of immobilized nucleic acids: theoretical concepts and practical considerations. Methods Enzymol. 1987;152:399–407. doi: 10.1016/0076-6879(87)52046-8. [DOI] [PubMed] [Google Scholar]
  24. Woltering E. J. Interorgan translocation of 1-aminocyclopropane-1-carboxylic Acid and ethylene coordinates senescence in emasculated cymbidium flowers. Plant Physiol. 1990 Mar;92(3):837–845. doi: 10.1104/pp.92.3.837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Woodson W. R., Park K. Y., Drory A., Larsen P. B., Wang H. Expression of ethylene biosynthetic pathway transcripts in senescing carnation flowers. Plant Physiol. 1992 Jun;99(2):526–532. doi: 10.1104/pp.99.2.526. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Yu Y. B., Yang S. F. Auxin-induced Ethylene Production and Its Inhibition by Aminoethyoxyvinylglycine and Cobalt Ion. Plant Physiol. 1979 Dec;64(6):1074–1077. doi: 10.1104/pp.64.6.1074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Zhang X. S., O'Neill S. D. Ovary and Gametophyte Development Are Coordinately Regulated by Auxin and Ethylene following Pollination. Plant Cell. 1993 Apr;5(4):403–418. doi: 10.1105/tpc.5.4.403. [DOI] [PMC free article] [PubMed] [Google Scholar]

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