Understanding vs. policies. Are you educating your people--or just training them?
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Biomedical subjects
Publications and source records attributed to T Dick.
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The expression of the chloramphenicol (Cm) - inducible Cm acetyltransferase gene (cat) of the staphylococcal plasmid pUB112 is regulated at the translational level. The leader mRNA preceding the cat coding sequence can form a stable hairpin structure, in which the cat Shine-Dalgarno sequence is masked. Previous work showed that translation of a short leader peptide terminating within the stem of the inhibitory secondary structure is required for basal Cm acetyltransferase (CAT) synthesis and its inducibility. In the present study we shortened this leader peptide by introducing ochre codons in its coding sequence and found that synthesis of the N-terminal part of the leader peptide, terminating directly 5' to the stem, is sufficient to mediate basal and inducible CAT synthesis. Amino acid substitution in this region of the leader peptide abolished inducibility. We suggest that the 5' region of the leader peptide coding sequence specifies a particularly Cm-sensitive translation that represents the Cm-sensor mechanism for cat gene induction.
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The gene for chloramphenicol (Cm) acetyltransferase (CAT) carried by the staphylococcal plasmid pUB112, whose expression can be stimulated by Cm, is preceded by a regulatory region containing two control elements. One of these consists of a Shine-Dalgarno (SD) sequence followed by an open reading frame coding for a leader peptide of nine amino acids. Previous work has shown that the SD sequence is essential for inducibility of Cm resistance by the antibiotic (Brückner and Matzura 1985). Here we demonstrate that fusion of the leader peptide coding sequence to a truncated 'lacZ gene results in synthesis of a leader peptide-beta-galactosidase fusion protein. Introduction of an ochre nonsense codon into the reading frame of the leader peptide sequence leads to considerable reduction of the basal expression and loss of inducibility of the cat gene. These results reveal that synthesis of the leader peptide is required for the basal and inducible expression of the cat gene and support the model of translational attenuation for its regulation.
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The purpose of this study was to analyze differences in the activity of medullary respiratory neurons in the unanesthetized, intact cat during wakefulness and non-rapid-eye-movement (NREM) sleep. We studied single respiratory neurons located within a 1-2 mm deep, 8-10 mm long zone that followed, and included in its dorsal aspect, the retrofacial and ambiguus nuclei. The analysis of variance was used to detect respiratory activity, and cycle-triggered histograms were plotted. The respiratory signal strength and consistency of the respiratory activity were quantified with the eta 2 statistic. We determined for each breath in wakefulness and NREM sleep the average discharge rate during the active phase of the cell, the number of action potentials during the active phase of the cell, and durations of both the cycle and inspiration. Differences in discharge rates and in the number of discharges between wakefulness and NREM sleep were tested with the t test. A bimodal distribution of eta 2 values for the population of neurons indicated there were two groups of respiratory cells: those with eta 2 values less than 0.3 and those with values greater than 0.3. The former we call weak respiratory cells; the latter, strong respiratory cells. Strong and weak cells were classified further as inspiratory or noninspiratory on the basis of the shape of their cycle-triggered histograms. Within the class of strong inspiratory cells, those with the highest eta 2 values 1) reached their peak discharge rate early, 2) discharged at high rates throughout inspiration, and 3) were inactive during expiration. The values of these variables diminished progressively in inspiratory cell groups with lower eta 2 values. Most cells were less active in NREM sleep than in wakefulness. Similar proportions of weak and strong cells and inspiratory and noninspiratory cells were affected by sleep. The reduction in sleep of the activity of strong inspiratory cells was consistent with a general relationship between this activity and the duration of inspiration. Lower discharge rates were associated with longer breaths; higher rates with shorter breaths. This relationship existed within both NREM sleep and wakefulness, and the plot of the relationship across these states formed a continuous function. The reduction in discharge rate in sleep was greater for weak than for strong inspiratory cells: the correlation coefficient between percent change in rate and eta 2 values was -0.636 for inspiratory cells, but it was not significant (-0.265) for noninspiratory cells.(ABSTRACT TRUNCATED AT 400 WORDS)
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This paper describes a prosthesis for patients who have had a partial amputation of the hand, or who have congenital absence of all or part of the hand. The prosthesis incorporates a new concept whereby the grip is operated by flexion and extension of the wrist. A covering for the prosthesis has been developed using a silicone polymer which produces a lifelike flexible glove. Thirteen patients have so far been fitted with this type of prosthesis, which can give good function and cosmesis.
The concerns of this study are taxonomic. We demonstrate a defining characteristic of respiratory neuronal activity. This characteristic is the degree or size of the respiratory component in the activity of a respiratory cell. The essential feature of respiratory activity is that it occurs in phase with some portion of the respiratory cycle. Therefore, neuronal activity can be arranged within a matrix in which the columns are fractions of the respiratory cycle and the rows are breaths and, as Netick and Orem (10) have shown, this matrix can be analyzed with an analysis of variance to determine whether the activity contains a respiratory component. However, the analysis of variance indicates nothing about the size of a statistically significant respiratory component. We hypothesized that the size of the respiratory component in the activity of different respiratory cells differed among cells but was a stable characteristic of any given cell. The index used to quantify the degree of respiratory activity was eta 2, the proportion of the total variance of the activity of a respiratory neuron consisting of the variance occurring across fractions of the respiratory cycle. This index theoretically depends on a) the range of activity levels across a respiratory cycle and the dispersion of activity levels over this range (parameters signifying the strength of the respiratory signal) and b) the variability in the activity of the cell across breaths (a parameter signifying the consistency of the respiratory activity). Theoretically, eta 2 values can vary from 0.0 to 1.0 indicating, respectively, that none or all of the variability in the activity of a cell across breaths is accounted for by a respiratory effect. eta 2 was used to analyze the size of the respiratory component in the activity of 32 medullary respiratory neurons recorded during nonrapid eye movement (NREM) sleep in chronic cats. These different respiratory cells had activity patterns with eta 2 values ranging from 0.1 to 0.9. However, the activity of a given cell produced eta 2 values that were consistent from sample to sample. Therefore, the eta 2 value of the activity of a cell was a defining, stable characteristic of that cell. The eta 2 values of the activity of the cells were strongly correlated with the consistency of their discharge pattern from breath to breath (r x,y = 0.975).(ABSTRACT TRUNCATED AT 400 WORDS)
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