Calcium control of glycogen synthase activities in mouse diaphragms, rat adipocytes and rat hepatocytes

The following article provides evidence that cellular calcium controls the activity of glycogen synthase in all three major glycogen storage tissues; muscle, fat, and liver. Depletion of cellular calcium resulted in a moderate increase of glycogen synthase %I activities in intact mouse diaphragms, in isolated rat adipocytes, and in rat hepatocytes. The increase in %I activity of glycogen synthase was more pronounced when the uridine di-phosphoglucose concentration in the glycogen synthase assay was lowered from 4.4 mM to 0.2 mM. Calcium depletion resulted in an approximately two-fold decrease in the Ka values for glucose-6-phosphate in all three tissues. The activities of glycogen synthase also correlated well with the content of cell-associated calcium in rat hepatocytes. The glucose-6-phosphate independent activities of glycogen synthase in extracts of calcium-replete and calcium-depleted tissue approached the same value following the exposure to crude phosphoprotein phosphatase. The activities of glycogen phosphorylase decreased in calcium-depleted tissues and cells. Insulin stimulated the activity of glycogen synthase in muscle and fat in the absence of added sugar and in the absence of extracellular calcium. It is concluded that glycogen synthase is under the control of calcium in the three main glycogen storage tissues. The actions of calcium are probably mediated through the actions of calcium-sensitive protein kinase(s).     

Size and fecundity variation in populations of Poecilia vivipara Block & Schneider (Teleostei; Poeciliidae) inhabiting an environmental gradient

The reproductive variables [female size (geometric centroid size), fecundity and offspring size (longest diameter of the embryo)] of the livebearer Poecilia vivipara in the quaternary lagoons of northern Rio de Janeiro State varied significantly among sites and were partially associated within and among sites. Mean female size was directly related to salinity. Fecundity (number of offspring) was directly related to female size both within and among sites. The female size × fecundity relationship, however, was not constant among sites. Offspring size was partially and directly associated with female size and salinity. The relationship between fecundity and female size was positively related with fecundity, suggesting a non-linear relationship of these variables when the total sample was considered. The results suggest that life-history differences among sites were more related to different predation regimes than to simple effects of plasticity caused by increased growth in saltwater environments.     

Fatty acid acylation of proteins in Physarum polycephalum

We have investigated the occurrence of protein-fatty acid acylation by metabolic incorporation of [3H]myristic and [3H]palmitic acids in Physarum polycephalum. We show that this organism contains fatty acylated proteins with mainly myristic acid covalently attached in alkali-stable linkages, probably amides. We find no evidence for ester-linked fatty acids, in contrast to the situation in vertebrate cells.