Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0038187 (starvation)
 24,951 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

It has previously been shown that the phenylalanine codon UUC encoding residue 8 of the Escherichia coli argI gene product, ornithine transcarbamylase, is misread as leucine at a high frequency during phenylalanine starvation. However, no misreading of the UUU encoding residue 3 was observed under these conditions. Using oligonucleotide-directed, site-specific mutagenesis, we have constructed mutants where these codons have been changed. Using these mutant argI genes we see a high level of mistranslation at position 8 during phenylalanine starvation whether the codon is UUU or UUC. With either codon at position 3 we see no leucine substitution. We also constructed a gene with a leucine codon at position 3. The product of this latter mutated gene is stable and active, indicating that preferential turnover of mistranslated protein is not obscuring an otherwise high rate of misreading. This would seem to indicate that it is the context rather than the particular phenylalanine codon which is important in determining these misreading levels.
Mol Gen Genet 1989 Sep
PMID:Context specific misreading of phenylalanine codons. 268 41

1. Rats submitted to starvation or water deprivation showed a decrease in LH and prolactin serum levels. 2. 5-HT was increased without changes in DA and NA in cerebral cortex of starved rats. 3. Neurotransmitters did not change in hypothalamus of starved rats but water deprivation decreased NA and increased 5-HT.
Gen Pharmacol 1989
PMID:Starvation and dehydration: effect on hypothalamic monoamines and serum LH and prolactin. 270 68

Whole and acid-separated serum samples from fed, starved, and refed Tilapia were analyzed for insulin-like growth factors 1 (IGF-1) and 2 (IGF-2) using human fetal brain radioreceptorassay (RRA-IGF-1), rat liver membrane radioreceptorassay (RRA-IGF-2), and radioimmunoassay (RIA-IGF-1). Triidothyronine (T3) and thyroxine (T4) levels were measured by commercial kits for RIA. For serum separation, acid Sephadex G-50 and G-100 and neutral Sephadex G-200 columns were used. Whole serum and separated serum cross-reacted in RRA-IGF-1, but only slightly in RRA-IGF-2. IGF activity eluted in two peaks after acid G-50 chromatography. Peak I eluted at the void volume, and peak II eluted with an apparent molecular weight of approximately 7 kDa. The 7 kDa activity did not cross-react in RIA-IGF-1 excluding identity with human intact or truncated IGF-1, but did suggest the presence of an IGF-1 variant form. Whole serum was separated over a neutral G-200 column, and all activity eluted at the void volume indicated an apparent molecular weight equal to or greater than 250 kDa. No IGF-binding activity was displayed by either whole serum or peak I after acid G-50 chromatography. Despite significant changes in body weight, an influence of starvation and refeeding on serum IGF activity could not be established. No correlation was seen between serum IGF and T3 and T4 levels.
Gen Comp Endocrinol 1989 May
PMID:The study of insulin-like growth factors in Tilapia, Oreochromus mossambicus. 271 23

To determine its map position, the sSP gene was cloned into plasmid pBR322 and the recombinant plasmid was integrated into the chromosome of a polA mutant at the site of the sSP gene by homologous recombination. The chromosomal location of Ampr was then determined by P1 phage-mediated transduction. Thus, the sSP gene was mapped between gltB and glnF at min 69.5 on the Escherichia coli chromosome. Strains were constructed in which the sSP gene was brought under the control of the lac regulatory system. This indicated that the stringent starvation protein (SSP) is dispensable for growth, at least under normal culture conditions.
Mol Gen Genet 1988 Mar
PMID:Genetic mapping of the Escherichia coli gene for the stringent starvation protein and its dispensability for normal cell growth. 283 36

In the freshwater pulmonate snail Lymnaea stagnalis glycogen synthesis in the glycogen storage cells (GC) is stimulated by increasing external glucose concentrations. On the other hand, a hyperglycemic factor from the CNS inhibits glycogen synthesis and stimulates glycogen breakdown in these cells. This CNS factor may be involved in the physiological control of glycogen mobilization. In the present study the interaction between the inhibiting effect of the CNS factor and the stimulating effect of increasing glucose concentrations on glycogen synthesis in isolated GC was investigated. The results, analyzed by determination of the Michaelis-Menten parameters for saturation kinetics, suggest that the CNS factor increases the glucose concentration required for half-maximal stimulation of glycogen synthesis, but does not influence the maximum rate of synthesis (competitive type of inhibition). The role of the hyperglycemic factor during conditions of glycogen breakdown was investigated by extirpation of the cerebral ganglia (-CG), which contain the main release sites of the factor. Extirpation did not affect the hemolymph glucose concentration or the glycogen levels in the GC during starvation. However, -CG animals showed reduced levels of the hyperglycemia normally associated with exposure to anaerobic conditions.
Gen Comp Endocrinol 1985 Aug
PMID:The hyperglycemic factor of the CNS of the freshwater snail Lymnaea stagnalis: interaction with glucose stimulation of glycogen synthesis and evidence for its release during anaerobiosis. 286 93

The pepN gene codes for aminopeptidase N whose expression is regulated at the transcriptional level by anaerobiosis and phosphate starvation. To define and characterize the functional region of the pepN promoter (pepNp), various promoter fragments were fused to the malPQ operon of Escherichia coli and transferred to the chromosome. The expression of the single copy operon fusion was measured by assaying the amylomaltase activity. Sequences upstream from the canonical promoter elements, located 110 to 60 bp preceding the transcription start site, are important for promoter functioning. This region plays a role in the expression of the two divergent promoters pepNp and pncBp. The regulation of pepNp under phosphate starvation was conserved in the various constructs in which pepNp is functional. However, no particular sequence specific for phosphate regulation was detected. In addition, the regulation of pncBp by Pi starvation was demonstrated.
Mol Gen Genet 1987 Dec
PMID:Deletion analysis of the promoter region of the Escherichia coli pepN gene, a gene subject in vivo to multiple global controls. 289 44

The effect of confinement and severe starvation on the plasma thyroxine (T4) and triiodothyronine (T3) concentrations was determined in emperor penguins (Aptenodytes forsteri). During their annual cycle, emperor penguins fast freely for periods of up to 4 months and may thus represent a unique subject to study endocrine adaptations to fasting. Plasma T4 concentrations progressively decreased following capture and confinement of naturally fasting penguins, and within 15-20 days stabilized at levels three times lower than in free-living penguins. A transient fourfold increase in plasma T3 concentration developed within the day following confinement in parallel with a rise in daily body mass loss. Both plasma T3 concentration and mass loss subsided to normal levels within 15 days. The decrease in plasma T4 concentration is in accordance with the well-known inhibitory effect of stress on thyroid function in birds and mammals, whereas the transient increase in plasma T3 concentration seems related to enhancement of energy expenditure as a consequence of restlessness. Starvation severe enough to exhaust fat stores and to activate protein catabolism induced a 6- and 5 to 10-fold fall in plasma T4 and T3, respectively. This is in marked contrast with maintenance of plasma thyroid levels during long-term natural fasting associated with protein sparing (R. Groscolas and J. Leloup (1986) Gen. Comp. Endocrinol. 63, 264-274). Surprisingly, there was a final reincrease in plasma T4 concentration in very lean penguins. These results suggest that the effect of starvation on plasma thyroid hormones seems to depend on how much protein catabolism is activated and demonstrate the acute sensitivity of thyroid hormone balance to stress in penguins.
Gen Comp Endocrinol 1989 Jan
PMID:The effect of severe starvation and captivity stress on plasma thyroxine and triiodothyronine concentrations in an antarctic bird (emperor penguin). 292 Aug 94

The effect of starvation on the corticosterone responses of immature cockerels to acute, novel stress has been determined. The marked corticosterone responses of fed birds to either horizontal treadmill exercise (0.04 km/hr) or intravenous adrenocorticotrophic hormone (ACTH) administration (P less than 0.001 in both cases) were reduced by starvation (P less than 0.01 and P less than 0.001, respectively). This reduction did not appear to be due to either feedback inhibition of corticosterone on the hypothalamus or pituitary, or to reduced adrenal responsiveness to endogenous ACTH. Starvation significantly elevated the basal level of circulating corticosterone (P less than 0.001), but the magnitude of this elevation and the level of corticosterone attained were less (P less than 0.05) in birds that were accustomed to starvation. This habituation of adrenocortical activity may be due to reduced pituitary ACTH secretion, and was specific in that the corticosterone responses to novel stressors were unaffected.
Gen Comp Endocrinol 1985 Jul
PMID:Adrenocortical responses to novel stressors in acutely or repeatedly starved chickens. 299 Oct 76

In order to clone the Escherichia coli gene for the stringent starvation protein (SSP), we determined its N-terminal sequence as well as the sequence of two peptide fragments obtained by cyanogen bromide cleavage of the protein. We then chemically synthesized four sets of oligodeoxyribonucleotide mixtures that represented possible codon combinations for parts of these amino acid sequences. The synthetic oligonucleotides were labelled with 32P at their 5'-termini and used as hybridization probes to detect DNA fragments containing the complementary sequences. Genomic Southern hybridization of E. coli chromosomal DNA gave up to ten DNA fragments hybridizing with each probe but only a few hybridized with two or more of the probes. The latter fragments were cloned in pBR322. By determining partial base sequences with a rapid method and examining proteins encoded by the DNA fragments, we were able to show that we had isolated a clone containing the complete SSP structural gene.
Mol Gen Genet 1985
PMID:Cloning of the Escherichia coli gene for the stringent starvation protein. 300 20

Starvation for phenylalanine led to leucine misincorporation frequencies of 0.1 and 0.6 at UUC codons in the argI transcript of Escherichia coli, but no detectable misincorporation at a UUU codon. Under similar starvation conditions the relative synthesis of full sized MS2 coat protein, encoded by the RNA virus or a DNA copy, is greatly reduced, preventing analysis of the protein. This reduction in amount is unaffected by a rpsL mutation.
Mol Gen Genet 1986 Jul
PMID:Mistranslation during phenylalanine starvation. 301 46


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