Abstract
Discs of avocado (Persea americana) fruit (15 x 3 mm thick) kept in a stream of moist air ripen within 72 h. Following cutting, a modest evolution of wound ethylene that dissipates in 24 h is followed by a burst of autocatalytic ethylene production associated with a respiratory climacteric, much as in the intact fruit. Aminoethoxyvinylglycine (AVG), an inhibitor of ethylene synthesis, and 2,5-norbornadiene (NBD) and Ag+, inhibitors of ethylene action, inhibit disc ripening, as does 2,4-dichlorophenoxyacetic acid (2,4-D), a synthetic auxin. On the other hand, none of the foregoing agents except Ag+, at concentrations that delay or prevent ripening, suppress the induction of four ripening-related genes encoding cellulase, polygalacturonase (PG), cytochrome P-450 oxidase (P-450), and ethylene-forming enzyme (EFE, or 1-aminopropane-1-carboxylic acid oxidase), respectively. Whereas Ag+ fully inhibits the production of cellulase and PG mRNAs, it has little effect on the induction of EFE and P-450 mRNAs. Cellulase and PG enzyme activities are absent in extracts of discs treated with AVG, NBD, or 2,4-D, as are antigenically detectable cellulase and PG proteins. The strong appearance of ripening-related mRNAs in discs inhibited from softening by ethylene antagonists suggests posttranscriptional control by ethylene. Similarly, inhibition of ripening by 2,4-D without suppression of mRNA induction suggests translational control. Whether ethylene inhibits transcription or postttranscriptional events or both depends on its concentration.
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Selected References
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- Almin K. E., Eriksson K. E., Jansson C. Enzymic degradation of polymers. II. Viscometric determination of cellulase activity in absolute terms. Biochim Biophys Acta. 1967 Jul 11;139(2):248–253. doi: 10.1016/0005-2744(67)90029-0. [DOI] [PubMed] [Google Scholar]
- Bozak K. R., Yu H., Sirevåg R., Christoffersen R. E. Sequence analysis of ripening-related cytochrome P-450 cDNAs from avocado fruit. Proc Natl Acad Sci U S A. 1990 May;87(10):3904–3908. doi: 10.1073/pnas.87.10.3904. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen K. H., Miller A. N., Patterson G. W., Cohen J. D. A Rapid and Simple Procedure for Purification of Indole-3-Acetic Acid Prior to GC-SIM-MS Analysis. Plant Physiol. 1988 Mar;86(3):822–825. doi: 10.1104/pp.86.3.822. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chirgwin J. M., Przybyla A. E., MacDonald R. J., Rutter W. J. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry. 1979 Nov 27;18(24):5294–5299. doi: 10.1021/bi00591a005. [DOI] [PubMed] [Google Scholar]
- Cohen J. D., Bausher M. G., Bialek K., Buta J. G., Gocal G. F., Janzen L. M., Pharis R. P., Reed A. N., Slovin J. P. Comparison of a commercial ELISA assay for indole-3-acetic Acid at several stages of purification and analysis by gas chromatography-selected ion monitoring-mass spectrometry using a c(6)-labeled internal standard. Plant Physiol. 1987 Aug;84(4):982–986. doi: 10.1104/pp.84.4.982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frenkel C. Involvement of Peroxidase and Indole-3-acetic Acid Oxidase Isozymes from Pear, Tomato, and Blueberry Fruit in Ripening. Plant Physiol. 1972 May;49(5):757–763. doi: 10.1104/pp.49.5.757. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lincoln J. E., Fischer R. L. Diverse mechanisms for the regulation of ethylene-inducible gene expression. Mol Gen Genet. 1988 Apr;212(1):71–75. doi: 10.1007/BF00322446. [DOI] [PubMed] [Google Scholar]
- McGarvey D. J., Sirevåg R., Christoffersen R. E. Ripening-related gene from avocado fruit : ethylene-inducible expression of the mRNA and polypeptide. Plant Physiol. 1992 Feb;98(2):554–559. doi: 10.1104/pp.98.2.554. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- 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]
- Theologis A. One rotten apple spoils the whole bushel: the role of ethylene in fruit ripening. Cell. 1992 Jul 24;70(2):181–184. doi: 10.1016/0092-8674(92)90093-r. [DOI] [PubMed] [Google Scholar]
- Tucker M. L., Laties G. G. Interrelationship of Gene Expression, Polysome Prevalence, and Respiration during Ripening of Ethylene and/or Cyanide-Treated Avocado Fruit. Plant Physiol. 1984 Feb;74(2):307–315. doi: 10.1104/pp.74.2.307. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Van der Straeten D., Van Wiemeersch L., Goodman H. M., Van Montagu M. Purification and partial characterization of 1-aminocyclopropane-1-carboxylate synthase from tomato pericarp. Eur J Biochem. 1989 Jul 1;182(3):639–647. doi: 10.1111/j.1432-1033.1989.tb14873.x. [DOI] [PubMed] [Google Scholar]
