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  • 1
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Plant Physiology and Plant Molecular Biology 53 (2002), S. 247-273 
    ISSN: 1040-2519
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Notes: Abstract Salt and drought stress signal transduction consists of ionic and osmotic homeostasis signaling pathways, detoxification (i.e., damage control and repair) response pathways, and pathways for growth regulation. The ionic aspect of salt stress is signaled via the SOS pathway where a calcium-responsive SOS3-SOS2 protein kinase complex controls the expression and activity of ion transporters such as SOS1. Osmotic stress activates several protein kinases including mitogen-activated kinases, which may mediate osmotic homeostasis and/or detoxification responses. A number of phospholipid systems are activated by osmotic stress, generating a diverse array of messenger molecules, some of which may function upstream of the osmotic stress-activated protein kinases. Abscisic acid biosynthesis is regulated by osmotic stress at multiple steps. Both ABA-dependent and -independent osmotic stress signaling first modify constitutively expressed transcription factors, leading to the expression of early response transcriptional activators, which then activate downstream stress tolerance effector genes.
    Type of Medium: Electronic Resource
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  • 2
    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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  • 3
    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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  • 4
    Electronic Resource
    Electronic Resource
    Copenhagen : Munksgaard International Publishers
    Physiologia plantarum 112 (2001), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Low temperature, drought and salinity are major adverse environmental factors that limit plant productivity. Understanding the mechanisms by which plants perceive and transduce these stress signals to initiate adaptive responses is essential for engineering stress-tolerant crop plants. Molecular and biochemical studies suggest that abiotic stress signaling in plants involves receptor-coupled phosphorelay, phosphoinositol-induced Ca2+ changes, mitogen-activated protein kinase cascades and transcriptional activation of stress-responsive genes. In addition, protein posttranslational modifications and adapter or scaffold-mediated protein-protein interactions are also important in abiotic stress signal transduction. Most of these signaling modules, however, have not been genetically established to function in plant abiotic stress signal transduction. To overcome the scarcity of abiotic stress-specific phenotypes for conventional genetic screens, molecular genetic analysis using stress-responsive promoter-driven reporter is suggested as an alternative approach to genetically dissect abiotic stress signaling networks in plants.
    Type of Medium: Electronic Resource
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  • 5
    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.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Under salt-stress conditions, Arabidopsis salt overly sensitive (sos) mutants show hypersensitive root growth. The sos gene products are involved in ion transport and signalling processes. To analyse salt-stress-responsive genes whose transcripts are regulated by the SOS signalling pathway, we used a 22K Agilent oligoarray and quantitative real-time polymerase chain reaction analyses. The amounts of transcripts of the major salt-inducible genes (RD29A/COR78, RD17/COR47, COR15A, KIN1, and RD22) in sos mutants were similar to those in the wild-type plants. These results indicate that the SOS3/SOS2 signalling pathway is independent of the DRE/CRT, ABRE, and MYC/MYB pathways. In sos2 mutants, the expression levels of 27 and 48 genes were up-regulated at least double under 2-h and 5-h salt stress conditions, respectively. Among the genes regulated by SOS2, we detected several encoding myb family transcription factors, AP2 transcription factors, and some ethylene-related, auxin-induced, and defence-related genes. On the other hand, expression levels of very few genes were different between sos3 mutant and wild-type plants. This observation indicates that the downstream SOS2 affects the regulation of stress-responsive genes much more strongly than the upstream SOS3. The gene expression profiles of sos2 and sos3 mutants were not identical. This indicates that SOS2 and SOS3 have individual roles in salt stress responses in addition to common roles.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 212 (1996), S. 101-106 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract N,N,N,N-tetrabutylsuccinylamide (TBSA) in a diluent composed of 50% trimethylbenzene (TMB) and 50% kerosene (OK) can extract uranyl (II) ion from nitric acid solution. The results of extraction study suggested the formation of the 1∶2∶1 uranyl (II) ion, nitrate ion and N,N,N,N-tetrabutylsuccinylamide complex as extracted specis. The values of thermodynamic functions have been calculated.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature biotechnology 21 (2003), S. 81-85 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] High concentrations of Na+ in saline soils inhibit plant growth and reduce agricultural productivity. We report here that CaMV 35S promoter driven overexpression of the Arabidopsis thaliana SOS1 gene, which encodes a plasma membrane Na+/H+ antiporter, improves plant salt tolerance in A. thaliana. ...
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-2048
    Keywords: Atriplex ; Gene expression ; NaCl regulation ; Halophyte ; Plasma-membrane H+-ATPase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An Atriplex nummularia L. cDNA probe encoding the partial sequence of an isoform of the plasma-membrane H+ -ATPase was isolated, and used to characterize the NaCl regulation of mRNA accumulation in cultured cells of this halophyte. The peptide (447 amino acids) translated from the open reading frame has the highest sequence homology to the Nicotiana plumbaginifolia plasma-membrane H+-ATPase isoform pma4 (greater than 80% identity) and detected a transcript of approximately 3.7 kb on Northern blots of both total and poly(A)+ RNA. The mRNA levels were comparable in unadapted cells, adapted cells (cells adapted to and growing in 342 mM NaCl) and deadapted cells (cells previously adapted to 342 mM NaCl that are now growing without salt). Increased mRNA abundance was detected in deadapted cells within 24 h after exposure to NaCl but not in unadapted cells with similar salt treatments. The NaCl up-regulation of message abundance in deadapted cells was subject to developmental control. Analogous to those reported for glycophytes, the plasma-membrane H+-ATPase are encoded by a multigene family in the halophyte.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-2048
    Keywords: Arabinogalactan protein ; Cell expansion ; Extracellular matrix ; Nicotiana ; Plasma membrane ; Salt stress
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cultured cells of tobacco (Nicotiana tabacum L.) adapted to 428 mM NaCl exhibited a reduced rate of cell enlargement, which is probably due to decreased cell-wall extensibility. Arabinogalactan-protein (AGP) has been implicated as a cell-wall-loosening factor (Schopfer 1990). Levels of plasma membrane and extracellular AGPs that react with Yariv reagent were measured and compared between NaCl-adapted and unadapted tobacco cells. Unadapted cells contained a very high level of AGPs on the plasma membrane, which amounted to 0.16 μg·μg−1 membrane protein. In contrast, AGPs were virtually undetectable on the plasma membrane of NaCl-adapted cells. Accumulation of AGPs was also decreased in culture media of NaCl-adapted cells. These data support the hypothesis that AGPs participate in cell expansion. Possible mechanisms of the proposed cell-expansion role of AGPs are discussed.
    Type of Medium: Electronic Resource
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