Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P56851 (epididymal)
 11,273 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The rat S14 gene encodes a protein of unknown function and has an amino acid sequence unrelated to any published sequences. Expression of mRNA S14 and lipogenesis in liver, fat, and mammary gland are regulated coordinately by dietary and hormonal stimuli, suggesting that the S14 protein may be associated with lipogenesis. Antisera to synthetic peptides corresponding to portions of the deduced amino acid sequence of the protein were used to identify the protein and to compare its regulation with that of mRNA S14. Antisera specifically recognized the in vitro translation product of mRNA S14 as defined by its migration on two-dimensional gel electrophoresis. A product of identical Mr was identified on Western blots of liver homogenates from hyperthyroid, carbohydrate-fed rats. Subcellular fractionation showed that S14 protein is primarily cytosolic. The protein was detectable in tissues with abundant S14 gene expression, including hyperthyroid liver and epididymal fat and hypothyroid brown adipose tissue, whereas it was undetectable in hypothyroid liver and euthyroid kidney, testis, and spleen. Diurnal variation in hepatic mRNA S14 correlated with comparable changes in levels of the protein. Surprisingly, no S14 protein was observed in the livers of chronically (3 week) hypothyroid rats treated with triiodothyronine (T3) until 12 h had elapsed, despite attainment of maximal levels of mRNA S14 within 4 h. Rapid appearance of protein after T3 treatment was observed in both euthyroid and short term (4 day) hypothyroid rats, suggesting that long-term hypothyroidism is associated with a defect in the translational efficiency of mRNA S14.
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PMID:Identification of rat S14 protein and comparison of its regulation with that of mRNA S14 employing synthetic peptide antisera. 258 93

Diurnal changes in glycogen stores of adipose tissues and in vitro lipolytic activity of isolated epididymal fat cells, and their lipolytic responsiveness to epinephrine and theophylline were examined in rats adapted to a 2-h daily meal feeding (20.00-22.00 h; darkness between 20.00-08.00 h) for 3 weeks and in control rats fed ad libitum. The fat cells from both groups of animals showed the peak of lipolytic activity at the mid-dark period (03.00 h), but the peak values and the average values at 6 or 7 time points examined within the 24-h feeding cycle were significantly higher (p less than 0.025) in meal-fed rats. Basal, epinephrine-stimulated, and epinephrine-induced lipolysis of fat cells from control rats showed diurnal changes, and the rhythms and their amplitude were affected by meal feeding. Changes in lipolytic activity of fat cells did not seem to relate directly to those of glycogen stores in adipose tissue. The over-all 24-h means of lipolytic activity of fat cells were significantly increased (p less than 0.001) with meal feeding. Mean cell size of epididymal fat pads was significantly smaller (p less than 0.001) in meal-fed rats, but lipolytic responsiveness to the graded concentrations of epinephrine and theophylline in the incubation medium was significantly greater (p less than 0.001) in meal-fed rats than in rats fed ad libitum. Thus, these findings suggest that lipolytic activity of the cAMP-hormone sensitive lipase system in fat cells might be increased with meal feeding in rats. Furthermore, the present results may give a new idea to consider the discrepancy that many workers have not been able to observe the increase in body fat deposition with meal feeding, which has been frequently reported to enhance lipogenesis in rats.
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PMID:Diurnal changes in lipolytic activity of isolated fat cells and their increased responsiveness to epinephrine and theophylline with meal feeding in rats. 668 56