Literature DB >> 16667866

Effects of Abscisic Acid and High Osmoticum on Storage Protein Gene Expression in Microspore Embryos of Brassica napus.

R W Wilen1, R M Mandel, R P Pharis, L A Holbrook, M M Moloney.   

Abstract

Storage protein gene expression, characteristic of mid- to late embryogenesis, was investigated in microspore embryos of rapeseed (Brassica napus). These embryos, derived from the immature male gametophyte, accumulate little or no detectable napin or cruciferin mRNA when cultured on hormone-free medium containing 13% sucrose. The addition of abscisic acid (ABA) to the medium results in an increase in detectable transcripts encoding both these polypeptides. Storage protein mRNA is induced at 1 micromolar ABA with maximum stimulation occurring between 5 and 50 micromolar. This hormone induction results in a level of storage protein mRNA that is comparable to that observed in zygotic embryos of an equivalent morphological stage. Effects similar to that of ABA are noted when 12.5% sorbitol is added to the microspore embryo medium (osmotic potential = 25.5 bars). Time course experiments, to study the induction of napin and cruciferin gene expression demonstrated that the ABA effect occurred much more rapidly than the high osmoticum effect, although after 48 hours, the levels of napin or cruciferin mRNA detected were similar in both treatments. This difference in the rates of induction is consistent with the idea that the osmotic effect may be mediated by ABA which is synthesized in response to the reduced water potential. Measurements of ABA (by gas chromatography-mass spectrometry using [(2)H(6)]ABA as an internal standard) present in microspore embryos during sorbitol treatment and in embryos treated with 10 micromolar ABA were performed to investigate this possibility. Within 2 hours of culture on high osmoticum the level of ABA increased substantially and significantly above control and reached a maximum concentration within 24 hours. This elevated concentration was maintained for 48 hours after culturing and represents a sixfold increase over control embryos. The ABA-treated embryos accumulated the hormone very quickly, but ABA concentrations returned to basal levels within 72 hours after treatment. The possibility that embryo-synthesized ABA may be a mediator of effects of osmotic stress on gene expression in Brassica embryos is discussed.

Entities:  

Year:  1990        PMID: 16667866      PMCID: PMC1077316          DOI: 10.1104/pp.94.3.875

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  11 in total

1.  Intracellular pH of Cotton Embryos and Seed Coats during Fruit Development Determined by P Nuclear Magnetic Resonance Spectroscopy.

Authors:  D L Hendrix; J W Radin; R A Nieman
Journal:  Plant Physiol       Date:  1987-10       Impact factor: 8.340

2.  A small-scale procedure for the rapid isolation of plant RNAs.

Authors:  T C Verwoerd; B M Dekker; A Hoekema
Journal:  Nucleic Acids Res       Date:  1989-03-25       Impact factor: 16.971

3.  Rapeseed embryo development in culture on high osmoticum is similar to that in seeds.

Authors:  R R Finkelstein; M L Crouch
Journal:  Plant Physiol       Date:  1986-07       Impact factor: 8.340

4.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

5.  Seed Storage Protein Transcription and mRNA Levels in Brassica napus during Development and in Response to Exogenous Abscisic Acid.

Authors:  A J Delisle; M L Crouch
Journal:  Plant Physiol       Date:  1989-10       Impact factor: 8.340

6.  Role of ABA in Maturation of Rapeseed Embryos.

Authors:  R R Finkelstein; K M Tenbarge; J E Shumway; M L Crouch
Journal:  Plant Physiol       Date:  1985-07       Impact factor: 8.340

7.  The development of an indirect enzyme linked immunoassay for abscisic Acid.

Authors:  G S Ross; P A Elder; J A McWha; D Pearce; R P Pharis
Journal:  Plant Physiol       Date:  1987-09       Impact factor: 8.340

8.  Regulation by ABA of beta-Conglycinin Expression in Cultured Developing Soybean Cotyledons.

Authors:  E A Bray; R N Beachy
Journal:  Plant Physiol       Date:  1985-11       Impact factor: 8.340

9.  Investigations on the Nature of the Auxin-Wave in the Cambial Region of Pine Stems : Validation of IAA as the Auxin Component by the Avena Coleoptile Curvature Assay and by Gas Chromatography-Mass Spectrometry-Selected Ion Monitoring.

Authors:  T J Wodzicki; H Abe; A B Wodzicki; R P Pharis; J D Cohen
Journal:  Plant Physiol       Date:  1987-05       Impact factor: 8.340

10.  In Vivo Inhibition of Seed Development and Reserve Protein Accumulation in Recombinants of Abscisic Acid Biosynthesis and Responsiveness Mutants in Arabidopsis thaliana.

Authors:  M Koornneef; C J Hanhart; H W Hilhorst; C M Karssen
Journal:  Plant Physiol       Date:  1989-06       Impact factor: 8.340

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  14 in total

1.  Oilbody Proteins in Microspore-Derived Embryos of Brassica napus: Hormonal, Osmotic, and Developmental Regulation of Synthesis.

Authors:  L A Holbrook; G J van Rooijen; R W Wilen; M M Moloney
Journal:  Plant Physiol       Date:  1991-11       Impact factor: 8.340

Review 2.  JIPs and RIPs: the regulation of plant gene expression by jasmonates in response to environmental cues and pathogens.

Authors:  S Reinbothe; B Mollenhauer; C Reinbothe
Journal:  Plant Cell       Date:  1994-09       Impact factor: 11.277

3.  Effects of jasmonic Acid on embryo-specific processes in brassica and linum oilseeds.

Authors:  R W Wilen; G J van Rooijen; D W Pearce; R P Pharis; L A Holbrook; M M Moloney
Journal:  Plant Physiol       Date:  1991-02       Impact factor: 8.340

4.  Endosperm cell division in maize kernels cultured at three levels of water potential.

Authors:  P N Myers; T L Setter; J T Madison; J F Thompson
Journal:  Plant Physiol       Date:  1992-07       Impact factor: 8.340

5.  Towards normalization of soybean somatic embryo maturation.

Authors:  M A Schmidt; D M Tucker; E B Cahoon; W A Parrott
Journal:  Plant Cell Rep       Date:  2005-04-22       Impact factor: 4.570

6.  Competitive Inhibition of Abscisic Acid-Regulated Gene Expression by Stereoisomeric Acetylenic Analogs of Abscisic Acid.

Authors:  R. W. Wilen; D. B. Hays; R. M. Mandel; S. R. Abrams; M. M. Moloney
Journal:  Plant Physiol       Date:  1993-02       Impact factor: 8.340

7.  Induction of Lipid and Oleosin Biosynthesis by (+)-Abscisic Acid and Its Metabolites in Microspore-Derived Embryos of Brassica napus L.cv Reston (Biological Responses in the Presence of 8[prime]-Hydroxyabscisic Acid).

Authors:  J. Zou; G. D. Abrams; D. L. Barton; D. C. Taylor; M. K. Pomeroy; S. R. Abrams
Journal:  Plant Physiol       Date:  1995-06       Impact factor: 8.340

8.  Far upstream activating promoter regions are responsible for expression of the BnC1 cruciferin gene from Brassica napus.

Authors:  P Bilodeau; J G Lafontaine; G Bellemare
Journal:  Plant Cell Rep       Date:  1994-12       Impact factor: 4.570

9.  Regulation of an Arabidopsis oleosin gene promoter in transgenic Brassica napus.

Authors:  A L Plant; G J van Rooijen; C P Anderson; M M Moloney
Journal:  Plant Mol Biol       Date:  1994-05       Impact factor: 4.076

10.  Effects of seed-specific expression of a cytokinin biosynthetic gene on canola and tobacco phenotypes.

Authors:  P Roeckel; T Oancia; J Drevet
Journal:  Transgenic Res       Date:  1997-03       Impact factor: 2.788

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