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  • 1
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Epigenetic regulation involves reversible changes in DNA methylation and/or histone modification patterns. Short interfering RNAs (siRNAs) can direct DNA methylation and heterochromatic histone modifications, causing sequence-specific transcriptional gene silencing. In animals and yeast, ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Plant Physiology and Plant Molecular Biology 51 (2000), S. 463-499 
    ISSN: 1040-2519
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Notes: Abstract Plant responses to salinity stress are reviewed with emphasis on molecular mechanisms of signal transduction and on the physiological consequences of altered gene expression that affect biochemical reactions downstream of stress sensing. We make extensive use of comparisons with model organisms, halophytic plants, and yeast, which provide a paradigm for many responses to salinity exhibited by stress-sensitive plants. Among biochemical responses, we emphasize osmolyte biosynthesis and function, water flux control, and membrane transport of ions for maintenance and re-establishment of homeostasis. The advances in understanding the effectiveness of stress responses, and distinctions between pathology and adaptive advantage, are increasingly based on transgenic plant and mutant analyses, in particular the analysis of Arabidopsis mutants defective in elements of stress signal transduction pathways. We summarize evidence for plant stress signaling systems, some of which have components analogous to those that regulate osmotic stress responses of yeast. There is evidence also of signaling cascades that are not known to exist in the unicellular eukaryote, some that presumably function in intercellular coordination or regulation of effector genes in a cell-/tissue-specific context required for tolerance of plants. A complex set of stress-responsive transcription factors is emerging. The imminent availability of genomic DNA sequences and global and cell-specific transcript expression data, combined with determinant identification based on gain- and loss-of-function molecular genetics, will provide the infrastructure for functional physiological dissection of salt tolerance determinants in an organismal context. Furthermore, protein interaction analysis and evaluation of allelism, additivity, and epistasis allow determination of ordered relationships between stress signaling components. Finally, genetic activation and suppression screens will lead inevitably to an understanding of the interrelationships of the multiple signaling systems that control stress-adaptive responses in plants.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Cultured tobacco cells (Nicotiana tabacum L. cv. Wisconsin 38) adapted to NaCl exhibited significant morphological and physiological changes. Adapted cells remained smaller and more isodiametric at maturity than unadapted cells. The vacuole increased in size relative to the cytoplasm and an extensive network of transvacuolar membrane strands developed. These changes altered the surface contact area between the cytoplasm and the vacuole substantially. In addition, the network of Hechtian strands that anchor the cortical structure to the cell wall became more extensively branched possibly facilitating surface contact of the cytoplasm to the extracellular matrix. Many changes in membrane proteins could also be identified after NaCl adaptation. In particular, a 50-kDa protein that is associated with the plasma membrane and tonoplast was induced during adaptation. Immunocytochemical localization indicated that this 50-kDa protein is associated with Golgi vesicles. By immunoscreening using anti-50-kDa antibody, a 1.71-kb cDNA clone (p50C) was isolated from a λ-ZAP cDNA expression library. The sequence of p50C did not show any significant identity with other genes. Because of the very low abundance of the p50C message, quantitative reverse transcription-polymerase chain reaction (RT-PCR) was used to analyze p50C gene expression. Immunoblot and quantitative RT-PCR analyses indicated that the expression of this gene is regulated developmentally since the mRNA and protein increased with age in salt-adapted cells but decreased with age in unadapted cells. Also in tobacco plants, p50C mRNA was more abundant in younger leaves than in older leaves. The gene was responsive to NaCl in tobacco cells and to ABA in tobacco seedlings.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Copenhagen : Munksgaard International Publishers
    Physiologia plantarum 104 (1998), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Griffonia simplicifolia leaf lectin II (GS-II) is a N-acetylglucosamine (GlcNAc) binding protein, consisting of large (rGS-II) and small (sGS-II) subunits, that is presumed to function in plant defense because both the holoprotein and the rGS-II inhibited insect growth and development in feeding bioassays. A cDNA encoding sGS-II has been isolated and the deduced peptide has sequence similarity to class III chitinases. However, neither the GS-II holoprotein nor bacterially expressed recombinant sGS-II proteins had detectable chitinase or lysozyme activities. Both rGS-II and sGS-II mRNAs accumulated in response to methyl jasmonate (Me-JA) treatment but not after wounding in local leaves unless injury was followed by treatment with the ethylene action inhibitor norbornadiene (NBD). Salicylic acid (SA) suppressed wounding/NBD induction of GS-II transcript accumulation and ethylene inhibited Me-JA-induced expression. Apparently, defensive gene expression induced by signal transduction through the octadecanoid pathway in local leaves is suppressed by stress induced ethylene that is produced as a consequence of wounding. However, in leaves systemic to the wound site, rGS-II mRNA levels increased substantially indicating that physiological levels of ethylene are insufficient to down regulate defensive gene expression away from the site of injury. It seems that G. simplicifolia has evolved a rather specialized response to herbivore attack whereby local activation of defensive gene expression is attenuated in order to mount a more substantial defense distal to the site of invasion.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 101 (1997), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Proline-overproducing carrot cell lines were isolated by selection in medium containing hydroxyproline, a toxic analogue of proline. During growth of the cells in culture, length of lag phase, doubling time, and maximum fresh weight were the same for the hydroxyproline-resistant cell line (HP) and the wild-type cell line (JW). Proline content and resistance to hydroxyproline in the HP and JW lines were not strictly correlated indicating that another reason besides the constitutive level of proline is involved in hydroxyproline resistance. Tolerance to polyethylene glycol-induced desiccation stress was not different between the two lines except perhaps at the early stages of culture growth when the proline levels of the two cell lines were nearly the same. The complexity of the relationship between proline accumulation and osmotolerance is discussed and strategies to achieve constitutive high levels of proline accumulation in plants are proposed.
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 95 (1995), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Arachidonic acid (AA), a fatty-acid fungal elicitor, and a cellulase preparation from Aspergillus niger, a protein-type fungal elicitor, induced osmotin gene expression. Both elicitors activated the osmotin promoter fused to a β-glucuronidase (GUS) reporter gene in a tissue-specific manner in tobacco seedlings (Nicotiana tabacum L. cv. Wisconsin 38). The cellulase preparation was more effective than AA at the concentrations tested and, unlike AA, also induced the accumulation of osmotin mRNA and protein. Combinations of AA and the cellulase preparation had a greater than additive effect on the activation of the osmotin promoter and the accumulation of osmotin mRNA and protein. Both AA and the cellulase preparation, when applied separately, were virtually ineffective in the induction of the osmotin promoter in cotyledon tissues. However, together they were able to induce synergistically GUS fused to the osmotin promoter. Increases in osmotin-promoter-driven GUS activity and accumulation of osmotin mRNA induced by AA, the cellulase preparation or their combination were reversed by norbornadiene, an ethylene action inhibitor, indicating that ethylene is involved in the induction of the osmotin gene by these elicitors.
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  • 7
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Heat-stable mycelial extracts of the nonpathogenic fungus Trichoderma longibrachiatum induced resistance in tobacco seedlings (Nicotiana tabacum L. cv. Wisconsin 38) to the pathogen Phytophthora parasitica var. nicotianae (race 0), which did not involve a hypersensitive response. Resistance could not be induced with mycelial extract prepared in the same manner from P. parasitica. The nonpathogenic mycelial extract induced expression of PR-1b and osmotin (PR-5) genes to a higher level than did mycelial extract from the pathogenic fungus. The tissue-specific pattern of PR gene induction by the nonpathogenic mycelial extract was different from that of the pathogenic mycelial extract and was consistent with the ability of the former to cause disease resistance. The expression patterns of these two PR genes and the accumulations of their encoded proteins also were affected by salicylic acid (SA), methyl jasmonate (MeJA), ethylene (E) and combinations of these plant signal messengers. However, only combined SA and MeJA treatment mimicked the pattern of PR gene mRNA and protein accumulation induced by the nonpathogenic mycelial extract. E inhibitors blocked both mycelial extract-induced and SA/MeJA-induced PR gene expression, and the cis pattern of responsiveness on the osmotin promoter was the same for the mycelial extract, SA, E, or E/MeJA. Seedlings treated with P. parasitica spores in the presence of SA/MeJA were protected from pathogen colonization. However, these seedlings exhibited symptoms of cell death (disease symptoms) both in the absence and presence of P. parasitica spores, in contrast to seedlings treated with nonpathogenic mycelial extract, which remained healthy. These results suggest that the signal transduction pathways for elicitation of defense responses by exogenously applied heat-stable nonpathogenic mycelial extract and SA/MeJA overlap at the point of PR protein induction but are not identical.
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  • 8
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Osmotin gene expression and protein synthesis were up-regulated in young tomato (Lycopersicon esculentum cv. Rheinlands Ruhm) plants after a short exposure (24 h) to 150 mM NaCl or 100 μM abscisic acid (ABA) or after dehydration to 80% of original plant fresh weight. Osmotically induced accumulation of osmotin mRNA was accompanied by a large increase in endogenous ABA levels. Increasing accumulation of osmotin protein was also observed during a longer exposure (7 days) to salt. Upon treatment with NaCl. osmotin mRNA levels increased in both root and leaf tissues. with an additional longer transcript induced in roots. No induction of osmotin mRNA was observed upon salt or water stress of the tomato ABA-deficient mutant sitiens. Treatment of sitiens with exogenous ABA induced osmotin mRNA accumulation to the level normally found in salt-treated wild-type plants. However, salt stress alone enhanced accumulation of osmotin mRNA in plants of another tomato mutant (flacca) which is also impaired in ABA synthesis. In tobacco plants carrying an osmotin promoter/β-glucuronidase (GUS) fusion gene, NaCl induction of GUS could be only partially blocked by the ABA inhibitor fluoridone. In flacca plants simultaneous treatment with NaCl and ABA resulted in higher levels of osmotin transcript compared to those following treatment with NaCl alone. No accumulation of osmotin protein was observed after short- or long-term osmotic treatments of the mutants. Our results support previous evidence that osmotin gene expression may be triggered in part through ABA and in part through a separate pathway of gene activation.
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  • 9
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: H6 is an Atriplex nummularia gene having high sequence homology with the algal caltractin (a basal-body-associated calcium-binding protein) gene. Recombinant H6 was expressed at high levels in Escherichia coli. The recombinant protein exhibited an ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid-induced mobility shift during sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and it was able to bind 45Ca2-. An H6 cDNA probe detected three RNA transcripts of 1.3, 2.2 and 2.4 kb, respectively. The levels of these transcripts were regulated by different environmental cues and during developmental stages. The steady state levels of the 1.3-kb mRNA decreased after touch and heat treatments. Expression of the 2.2-kb message correlated with cell proliferation activity. In cultured cells, the highest level of the 2.2-kb message preceeded the peak of mitotic cell division activity. In plants, the 2.2-kb message was detected only in shoot tips that contained meristematic tissues. The 2.4-kb message was detected exclusively in heat-shocked cells. The relationship among the three transcripts is discussed in the context of the possible role of H6 in mediating developmental and environmental signals.
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 48 (1980), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Addition of plant growth regulators (5 nM NAA and 5μM BAP) to a defined basal medium stimulated adventitious bud formation of Douglas fir (Pseudotsuga menziesii [Mirb.] Franco) cotyledon explants in culture. Cytoplasmic soluble proteins synthesized during early stages of adventitious bud formation were analyzed by electrophoresis of 3H- and 14C-leucine labeled proteins on SDS polyacrylamide gels. Increased synthesis of low molecular weight proteins (16,000 to 20,000 daltons) was detected after 2 days in culture and reached a maximal level at day 4. When cotyledon explants cultured on bud medium for 2 days were transferred to callus medium (which suppressed adventitious bud formation), suppression of the synthesis of low molecular weight proteins was also observed, suggesting that these proteins may be associated with early stages of adventitious bud formation.
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