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31.
We report a new technique using fluorescent probes to detect a mRNA and a protein simultaneously in the Drosophila embryo. For in situ hybridization, 3-hydroxy-N-2′-biphenyl-2-naphthalenecarboxamide phosphate ester (HNPP)/Fast Red TR was used as a fluorescent substrate for alkaline
phosphatase. It was possible to compare protein and mRNA expression on a cell by cell basis with a laser scanning confocal
microscope. We applied this technique to analyse the dynamics of Distal-less (Dll) enhancer activity in the thoracic limb primordium in the early Drosophila embryo. We stained embryos bearing the Dll early enhancer (Dll-304) fused to the Escherichia coli lacZ gene. LacZ mRNA was detectable in the ventral region of the limb primordium, and β-galactosidase protein in the dorsal region. In the
middle, both mRNA and protein were detectable. These results suggest that the Dll enhancer is activated in the ventral region of the limb primordium and that Dll-positive cells migrate from a ventral position to a dorsal one within a single limb primordium.
Received: 7 April 1997 / Accepted: 15 May 1997 相似文献
32.
33.
34.
Dye-flow apparatus to measure the variation in axial xylem permeability over a stem cross-section 总被引:1,自引:1,他引:0
R. E. BOOKER 《Plant, cell & environment》1984,7(8):623-628
Abstract Equipment and methodology are described that allows the radial variation in axial xylem permeability (hydraulic conductivity) over a tree cross-section to be measured and the flow paths to be identified by the strictly controlled flow of dye through a specimen. The apparatus can be calibrated so that the point-to-point variation of absolute permeability over a xylem cross-section can be calculated from the dye-flow patterns, which otherwise show only relative variations in permeability. The effect of using different dyes and dye concentrations on the penetration time and the shape of the dye patterns was investigated. The penetration time through the wood of identical end-matched specimens is appreciably longer for fixing dyes than for non-fixing dyes, and for the fixing dyes it depends strongly on the dye concentration. However, the dye patterns of the end-matched specimens were indistinguishable with fixing and non-fixing dyes, and independent of dye concentration. The fixing dye toluidine blue at 0.25% to 0.5% (w/w) was found most suitable as it yields a clear permanent pattern. 相似文献
35.
A highly sensitive fluorimetric assay using 3-O-methylfluorescein phosphate as substrate was used in the determination of K+-dependent phosphatase activity in preparations of rat skeletal muscle. The gastrocnemius muscle was chosen because of mixed fibre composition. Crude, detergent treated homogenate was used so as to avoid loss of activity during purification. K+-dependent phosphatase activities in the range 0.19–0.37 μmol · (g wet weight)−1 · min−1 were obtained, the value decreasing with age and K+-deficiency. Complete inhibition of the K+-dependent phosphatase was obtained with 10−3 M ouabain. Using a KSCN-extracted muscle enzyme the intimate relation between K+-dependent phosphatase activity and (Na+ + K+)-activated ATP hydrolysis could be demonstrated. A molecular activity of 620 min−1 was estimated from simultaneous determination of K+-dependent phosphatase activity and [3H]ouabain binding capacity using the partially purified enzyme preparation. The corresponding enzyme concentration in the crude homogenates was calculated and corresponded well with the number of [3H]ouabain binding sites measured in intact muscles or biopsies hereof. 相似文献
36.
The time-resolved fluorescence emission anisotropy of 12-(9-anthroyloxy)stearic acid (12-AS) and 1,6-diphenyl-1,3,5-hexatriene (DPH) have been measured in dipalmitoylphosphatidylcholine liposomes in the presence and absence of 40 mol% cholesterol at temperatures above and below the phase transition temperature (41°C). By using a synchronously-pumped mode-locked frequency-doubled dye laser and single photon counting detection with an excitation response function of 300 picosecond, rotational correlation times down to less than 1 nanosecond could be resolved. Whereas DPH showed only small changes in the limiting anisotropy on the addition of cholesterol, 12-AS showed significant increases in this parameter with the effect being potentiated at higher temperatures. This difference in behaviour has been attributed to a fluorophore-cholesterol interaction that resulted in a change in the fluorophore geometry. Not only do DPH and 12-AS sense different depolarizing rotations due to the different directions of their emission dipoles but also differ in their lipid interactions which alter their limiting anisotropies. The implication is that the comparison of steady-state anisotropy measurements between chemically identical fluorophores in different lipid environments may be complicated by molecular distortions that change the motions to which the steady-state fluorescence parameters will be sensitive. 相似文献
37.
Randi B. Silver Gustavo Frindt Lawrence G. Palmer 《The Journal of membrane biology》1992,125(1):13-24
Summary Changes in intracellular pH (pH
i
) were measured using the pH indicator, BCECF, in principal cells from split opened cortical collecting tubules (CCTs) derived from rabbits maintained on a normal diet. This monolayer preparation has the advantage of allowing us to visualize the morphological differences in the two major cell types in this nephron segment under transmitted light. The visual identification of the cell types was verified using emission measurements taken from single principal and intercalated cells in the opened tubule which had been exposed to fluorescein isothiocyanate (FITC)-labeled peanut lectin. We confirmed the existence of an amiloride-sensitive Na/H exchange process activated during intracellular acidosis in principal cells. In addition, the exchanger was active under basal conditions and over a wide range of pH
i
. Because the exchanger was active under basal conditions we tested the hypothesis that changes in intracellular Na (Na
i
) would alter pH
i
in a predictable way. Maneuvers designed to alter Na
i
were without significant effects within a 10-min time frame. Specifically, addition of 100 m ouabain to increase Na
i
or exposure of the tubules to 10–5
m amiloride to decrease luminal Na entry and reduce Na
i
did not have an effect on pH
i
. In some experiments we did observe however, after a 30-min exposure to ouabain, a small decrease in pH
i
. These results suggest that Na/H exchange is a major regulator of pH
i
in principal cells. However, regulation of Na transport by changes in pH
i
in principal cells of rabbit CCT via the activity of a Na/H exchanger do not seem to contribute to the feedback control of Na transport.This work was supported by U.S. Public Health Service grants DK27847 to L.G. Palmer and DK11489 to E.E. Windhager. 相似文献
38.
Fluorescent microscopy was proved to be effective for structural identification of permineralized plant tissues in calcite
nodules from the Upper Cretaceous of Hokkaido, Japan. A minute, scale-like projection on the bract of a fossil Taxodiaceous
cone is identified as a true ovuliferous scale because it is bordered with a continuous epidermis that exhibits prominent
fluorescence. The presence of the ovuliferous scale suggests that the fossil is aTaiwania archetype. 相似文献
39.
40.
31P-Nuclear-magnetic-resonance spectra of maize (Zea mays L.) root tips, that had been induced to extrude large amounts of H+ in response to fusicoccin (FC) in the presence of potassium salts, indicate that the cytoplasmic pH does not become higher than that of controls. In fact, the cytoplasmic pH may become slightly (approx. 0.1 pH unit) lower in cells extruding H+. Estimations of the buffer capacity of the cells show that without active intracellular pH regulation, H+ extrusion caused by FC would cause the intracellular pH to rise by at least 0.6 pH unit h-1. Our results indicate that intracellular pH is tightly regulated even during extreme rates of acid extrusion, and that a rise in cytoplasmic pH is not the signal linking H+ extrusion with enhanced organic-acid synthesis or other intracellular responses to H+ pumping.Abbreviations FC
fusicoccin
- Pi
inorganic phosphate
- NMR
nuclear magnetic resonance
-
chemical shift
- MDP
methylene diphosphonic acid 相似文献