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21.
Replicon rescue: a novel strategy to clone the genomic DNA flanking insertions of integrating shuttle vector DNA.
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T L McMahon Z Wilczynska C Barth D J Fraser L Pontes P R Fisher 《Nucleic acids research》1996,24(20):4096-4097
A novel cloning strategy, replicon rescue, was developed for cloning genes disrupted by plasmid insertions. After ligation to a tetracycline resistance cassette, fragments containing a bacterial origin of replication from the insertion are recovered in Escherichia coli because they replicate autonomously. Restriction enzymes for cloning are so chosen that the only legitimate two fragment ligation yielding TetR clones involves a fragment spanning the boundary of the insertion. Replicon rescue was used successfully firstly in a test system to clone the chromosomal orl from a Klebsiella aerogenes strain, and secondly to recover a disrupted gene from a phototaxis-deficient mutant of Dictyostelium. 相似文献
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Murielle Rinaldi-Carmona Francis Barth Michel Haulme David Shire Bernard Calandra Christian Congy Serge Martinez Jeanne Maruani Gervais Nliat Daniel Caput Pascual Ferrara Philippe Soubri Jean Claude Brelire Grard Le Fur 《FEBS letters》1994,350(2-3):240-244
SR141716A is the first selective and orally active antagonist of the brain cannabinoid receptor. This compound displays nanomolar affinity for the central cannabinoid receptor but is not active on the peripheral cannabinoid receptor. In vitro, SR141716A antagonises the inhibitory effects of cannabinoid receptor agonists on both mouse vas deferens contractions and adenylyl cyclase activity in rat brain membranes. After intraperitoneal or oral administration SR141716A antagonises classical pharmacological and behavioural effects of cannabinoid receptor agonists. This compound should prove to be a powerful tool for investigating the in vivo functions of the anandamide/cannabinoid system. 相似文献
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D. Baurecht F. G. Barth 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1993,173(3):309-319
We analyzed the response of the vibration sensitive lyriform organ on the metatarsus of female spiders (Cupiennius salei) to dummies of male courtship vibrations. One of the two representative slits studied is sharply tuned to 500 Hz. Only the other slit is sensitive enough at lower frequencies to represent the parameters contained in the behaviourally effective dummies:
- Amplitude. The physiological threshold is similar to the behavioural threshold. The stimulus acceleration amplitudes leading to a good synchronization between response and temporal stimulus pattern coincide with those effectively eliciting a behavioural response. The most frequent spike intervals remain nearly constant in this range. At acceleration amplitudes above the natural range, syllable and pause durations are misrepresented by the receptor response.
- Frequency. Varying the carrier frequency between 35–500 Hz changes the most frequent spike intervals. Interval histograms resulting from behaviourally effective stimuli (50–200 Hz), however, are similr for carrier frequencies differing by a factor of 2.
- Temporal pattern. Response duration reflects the temporal parameters of the stimulus. The most frequent spike interval only changes with temporal stimulus characteristics far off the natural range. The number of spikes during a syllable decreases in ongoing stimulus series. The quality of copying the temporal stimulus pattern remains unchanged, however.
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Summary In Cupiennius salei (Ctenidae), as in other spiders, the central nervous system is divided into the supraoesophageal ganglion or brain and the suboesophageal ganglia (Fig. 1). The two masses are interconnected by oesophageal connectives. The brain gives off four pairs of optic and one pair of cheliceral nerves. From the suboesophageal ganglia arise a pair of pedipalpal, four pairs of leg, and several pairs of opisthosomal nerves (Fig. 2).
1. Cell types. In the brain a total of 50900 cells were counted, in the suboesophageal ganglia 49000. They are all monopolar cells, found in the ganglion periphery and may be classified into four types: (a) Small globuli cells (nuclear diameter 6–7 m) forming a pair of compact masses in the protocerebrum (Fig. 10b); (b) Small and numerous cells (cell diameter 12–20 m) with processes forming the bulk of the neuropil in the brain and suboesophageal ganglia; (c) Neurosecretory cells (cell diameter ca. 45 m) in the brain and suboesophageal ganglia; (d) Large motor and interneurons (cell daimeter 40–112 m), mostly in the suboesophageal ganglia (Figs. 10a and c).
2. Suboesophageal mass. The cell bodies form a sheet of one to several cell layers on the ventral side of each ganglion and are arranged in groups. Three such groups were identified as motor neurons, four as interneurons. At the dorsal, dorso-lateral, and mid-central parts of the ganglion there are no cell somata. The fibre bundles arising from them form identifiable transverse commissural pathways (Fig. 9b). They form the fibrous mass in the central part of the suboesophageal mass.Neuropil is well-formed in association with the sensory terminations of all major nerves (Fig. 9a). As these proceed centrally they break up into five major sensory tracts forming five layers one above the other. There are six pairs of additional major longitudinal tracts arranged at different levels dorsoventrally (Fig. 8). They ascend into the brain through the oesophageal connectives and terminate mostly in the mushroom bodies and partly in the central body.
3. Protocerebrum. Fine processes of the globuli cells form the most important neuropil mass in the fibrous core, called the mushroom bodies. These consist of well developed glomeruli, hafts, and bridge which are interconnected with the optic masses of the lateral eyes and most fibre tracts from the brain and suboesophageal mass (Fig. 7). The median eye nerves form a small optic lamella and optic ganglia, connected to the central body through an optic tract. Each posterior median and posterior lateral eye nerve ends in large optic lamellae (Fig. 13a). These are connected through chiasmata to a large optic mass where fibres from globuli cells form conspicuous glomeruli. There are 10–12 large fibres (diameter 9 m) of unknown origin on each side, terminating in the optic lambella of the posterior lateral eye.The central body, another neuropil mass (Fig. 13b) in the protocerebrum, is well developed in Cupiennius and located transversely in its postero-dorsal region (Fig. 10d). It consists of two layers and is interconnected with optic masses of the median and lateral eyes through optic tracts. Fibre tracts from the brain and suboesophageal mass join the central body. 相似文献
27.
Effects of low-chloride solutions on action potentials of sheep cadiac purkinje fibers 总被引:2,自引:0,他引:2
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The rapid repolarization during phase 1 of the action potential of sheep cardiac purkinje fibers has been attributed to a time- and voltage-dependent chloride current. In part, this conclusion was based on experiments that showed a substantial slowing of phase 1 when larger, presumably impermeant, anions were substituted for chloride in tyrode’s solution. We have re- examined the electrical effects of low-chloride solutions. We recorded action potentials of sheep cardiac purkinje fibers in normal tyrode’s solution and in low-chloride solutions made by substituting sodium propionate, acetylglycinate, methylsulfate, or methanesulfonate for the NaCl of Tyrode’s solution. Total calcium was adjusted to keep calcium ion activity of test solutions equal to that of control solutions. Propionate gave qualitatively variable results in preliminary experiments; it was not tested further. Low-chloride solutions made with the other anions gave much more consistent results: phase 1 and the notch that often occurs between phases 1 and 2 were usually unaffected, and the action potential duration usually increased. The only apparent change in the resting potential was a transient 3-6 mV depolarization when low-chloride solution was first admitted to the chamber, and a symmetrical transient hyperpolarization when chloride was returned to normal. If a time- and voltage-dependent chloride current exists in sheep cardiac purkinje fibers, our results suggest that it plays little role in generating phase 1 of the action potential. 相似文献
28.
Map of plasmid RP4 derived by insertion of transposon C. 总被引:21,自引:0,他引:21
We have determined the location of 36 sites on plasmid RP4 into which transposon C (an 8.5 × 106 molecular weight DNA sequence conferring trimethoprim and streptomycin resistance) had spontaneously inserted itself. These were located by sucrose gradient analysis of EcoRI-generated and then, separately, the HindIII-generated DNA fragments from each RP4-TnC2 plasmid. RP4 has a single EcoRI-susceptible site and, suitably displaced from this, a HindIII-susceptible site, whereas TnC has, respectively, one and two sites for these two enzymes. Thus the sizes of the restriction fragments depend on the location and orientation of the inserted TnC.Some of the RP4-TnC clones had lost one of the RP4 characters: transferability (Tra), tetracycline (Tc) or kanamycin (Km) resistances, but no ampicillin (Ap) sensitive clones were detected. Insertions giving each of these phenotypic changes cluster together at positions on the circular RP4 map that presumably locate the genes responsible for the Tra+, Kmr and Tcr phenotypes. The Tra? plasmids were grouped into four classes on the basis of their conferred phage sensitivities and plasmid copy numbers. The gene giving Apr was located by its known proximity to a BamHI-susceptible site. All the plasmids analysed had TnC inserted with one particular orientation. TnC insertions giving no detectable phenotypic change were not randomly placed around RP4, but clustered into certain regions. Two large regions, one containing TnA, had no TnC insertions. Ligation experiments with restriction fragments from various RP4-TnC plasmids led to the conclusion that both these regions contain genes essential to the replication and maintenance of RP4. The location of the HindIII site of RP4 within the gene giving Kmr should prove valuable to the use of this plasmid as a cloning vehicle. 相似文献
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