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171.
Howard A. Bern Robert Gunther Donald W. Johnson Richard S. Nishioka 《Acta zoologica》1973,54(1):15-19
- 1 Urotensin II (bladder-contracting activity) is present in the caudal spinal cords of teleosts, elasmobranchs, holosteans, and chondrosteans, in order of decreasing activity. It is questionably present in holocephalans and probably absent from lungfishes.
- 2 Cyclostomes and tailed amphibians show no evidence for any specific caudal urotensin II.
- 3 The pharmacological evidence parallels the cytological evidence for the occurrence of a caudal neurosecretory system.
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173.
Preferential expression of a plant cystatin at nematode feeding sites confers resistance to Meloidogyne incognita and Globodera pallida 总被引:2,自引:0,他引:2
The expression patterns of three promoters preferentially active in the roots of Arabidopsis thaliana have been investigated in transgenic potato plants in response to plant parasitic nematode infection. Promoter regions from the three genes, TUB-1, ARSK1 and RPL16A were linked to the GUS reporter gene and histochemical staining was used to localize expression in potato roots in response to infection with both the potato cyst nematode, Globodera pallida and the root-knot nematode, Meloidogyne incognita. All three promoters directed GUS expression chiefly in root tissue and were strongly up-regulated in the galls induced by feeding M. incognita. Less activity was associated with the syncytial feeding cells of the cyst nematode, although the ARSK1 promoter was highly active in the syncytia of G. pallida infecting soil grown plants. Transgenic potato lines that expressed the cystatin OcIDeltaD86 under the control of the three promoters were evaluated for resistance against Globodera sp. in a field trial and against M. incognita in containment. Resistance to Globodera of 70 +/- 4% was achieved with the best line using the ARSK1 promoter with no associated yield penalty. The highest level of partial resistance achieved against M. incognita was 67 +/- 9% using the TUB-1 promoter. In both cases this was comparable to the level of resistance achieved using the constitutive cauliflower mosaic virus 35S (CaMV35S) promoter. The results establish the potential for limiting transgene expression in crop plants whilst maintaining efficacy of the nematode defence. 相似文献
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176.
W. Ellis Penning Marit Mjelde Bernard Dudley Seppo Hellsten Jenica Hanganu Agnieszka Kolada Marcel van den Berg Sandra Poikane Geoff Phillips Nigel Willby Frauke Ecke 《Aquatic Ecology》2008,42(2):237-251
Aquatic macrophytes are one of the biological quality elements in the Water Framework Directive (WFD) for which status assessments
must be defined. We tested two methods to classify macrophyte species and their response to eutrophication pressure: one based
on percentiles of occurrence along a phosphorous gradient and another based on trophic ranking of species using Canonical
Correspondence Analyses in the ranking procedure. The methods were tested at Europe-wide, regional and national scale as well
as by alkalinity category, using 1,147 lakes from 12 European states. The grouping of species as sensitive, tolerant or indifferent
to eutrophication was evaluated for some taxa, such as the sensitive Chara spp. and the large isoetids, by analysing the (non-linear) response curve along a phosphorous gradient. These thresholds
revealed in these response curves can be used to set boundaries among different ecological status classes. In total 48 taxa
out of 114 taxa were classified identically regardless of dataset or classification method. These taxa can be considered the
most consistent and reliable indicators of sensitivity or tolerance to eutrophication at European scale. Although the general
response of well known indicator species seems to hold, there are many species that were evaluated differently according to
the database selection and classification methods. This hampers a Europe-wide comparison of classified species lists as used
for the status assessment within the WFD implementation process. 相似文献
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The association of the prion protein (PrP) with sphingolipid- and cholesterol-rich lipid rafts is instrumental in the pathogenesis of the neurodegenerative prion diseases. Although the glycosylphosphatidylinositol (GPI) anchor is an exoplasmic determinant of raft association, PrP remained raft-associated in human neuronal cells even when the GPI anchor was deleted or substituted for a transmembrane anchor indicating that the ectodomain contains a raft localization signal. The raft association of transmembrane-anchored PrP occurred independently of Cu(II) binding as it failed to be abolished by either deletion of the octapeptide repeat region (residues 51-90) or treatment of cells with a Cu(II) chelator. Raft association of transmembrane-anchored PrP was only abolished by the deletion of the N-terminal region (residues 23-90) of the ectodomain. This region was sufficient to confer raft localization when fused to the N terminus of a non-raft transmembrane-anchored protein and suppressed the clathrin-coated pit localization signal in the cytoplasmic domain of the amyloid precursor protein. These data indicate that the N-terminal region of PrP acts as a cellular raft targeting determinant and that residues 23-90 of PrP represent the first proteinaceous raft targeting signal within the ectodomain of a GPI-anchored protein. 相似文献
180.
Ernst H. Oliw Lena Hrnsten Howard Sprecher 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》1997,690(1-2):332-337
Prostaglandin H synthase-1 of ram vesicular glands metabolises 5,8,11-eicosatrienoic (Mead) acid to 13R-hydroxy-5,8,11-eicosatrienoic and to 11R-hydroxy-5,8,12-eicosatrienoic in a 5:1 ration. We wanted to determine the metabolism of this fatty acid by prostaglandin H synthase-2. Western blot showed that microsomes of sheep and rabbit placental cotyledons contained prostaglandin H synthase-2, while prostaglandin H synthase-1 could not be detected. Microsomes of sheep cotyledons metabolised [1-14C]5,8,11-eicosatrienoic acid to many polar metabolites and diclofenac (0.05 mM) inhibited the biosynthesis. The two major metabolites were identified as 13-hydroxy-5,8,11-eicosatrienoic and 11-hydroxy-5,8,12-eicosatrienoic acids. They were formed in a ratio of 3:2, which was not changed by aspirin (2 mM). 5,8,11-Eicosatrienoic acid is likely oxygenated by removal of the pro-S hydrogen at C-13 and insertion of molecular oxygen at either C-13 or C-11, which is followed by reduction of the peroxy derivatives to 13-hydroxy-5,8,11-eicosatrienoic and 11-hydroxy-5,8,12-eicosatrienoic acids, respectively. Prostaglandin H synthase-1 and -2 oxygenate 5,8,11-eicosatrienoic acid only slowly compared with arachidonic acid. 相似文献