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Y Natori

Publications and source records attributed to Y Natori.

At least 163 records · Page 9Linked to original sources

Turnover of rat liver 28 S ribosomal RNA: nicking as the initial step of degradation.

The large ribosomal subunits of rat liver contain small amount of minor RNA components which migrate through polyacrylamide gels between the two major rRNAs, and some 28 S rRNA molecules contain hidden nicks which can be revealed by heat treatment. The minor RNA components were isolated, labeled in vitro with 125I, and hybridized with nucleolar DNA from rat liver. The hybridization-competition experiments with 28 S RNA established that the minor RNA components and 28 S rRNA have a common DNA origin. When RNA components were isolated from rats that had received [14C]orotate and [3H]orotate, 1 week and 16 h, respectively, before sacrifice, the 14C : 3H ratio was the highest in the minor components, followed by the nicked RNA, and the intact 28 S rRNA showed the lowest ratio. We also found that partial hepatectomy decreases and the actinomycin C-treatment increases the amount of the minor RNA components as well as the nicked 28 S RNA. From these observations, we conclude that the initial step of degradation of 28 S rRNA in vivo is the nick formation and that the nicked RNA subsequently gives rise to the minor components.

Animals↗

Induction of globin gene expression in cultured erythroleukemia cells by butyric acid.

Butyric acid induces erythroid differentiation of cultured Friend leukemia cells when added to the culture medium. A high level of globin messenger RNA (mRNA) was detected in Friend leukemia cells treated with butyric acid by a liquid hybridization method using radioactive DNA complementary to reticulocyte globin mRNA. The content of globin mRNA molecules induced in the cytoplasm of the butyric acid-treated Friend leukemia cells paralleled the hemoglobin content determined by the benzidine staining method. Therefore, this hemoglobin synthesis may be most reasonably explained in terms of transcriptional activation of globin genes, as previously proposed in the case of dimethylsulfoxide, another inducer of erythroid differentiation. Induced accumulation of globin mRNA in the nuclei also supports this interpretation.

Animals↗

Molecular-size-dependent degradation of liver cytosolic proteins in vitro.

Degradation of rat liver cytosolic proteins at a neutral pH in the presence of 0.1% SDS was demonstrated by SDS-acrylamide gel electrophoresis. This proteolysis in vitro mimics molecular-size-dependent proteolysis in vivo; larger proteins were degraded more rapidly than smaller ones. Evidence is presented that the proteolysis is not due to contaminating lysosomal cathepsins in the cytosol.

Animals↗

The state of lysosomes and protein turnover in rat liver. Effect of excess vitamin A.

Administration of excess vitamin A to rats induces labilization of liver lysosomal membranes, as shown by the release of lysosomal cathepsins upon tissue homogenization. The effect of lysosomal labilization on liver protein turnover was investigated. The apparent turnover rate of liver proteins in the hypervitaminotic animals, as measured by a double isotope-labeling technique (Glass and Doyle (1972) J, Biol. Chem, 247, 5234-5242), was found to be the same as that in control animals. Neutral and alkaline fructose-1, 6-biphosphatase [EC 3.3.3.11] activities in the liver were also found to be unchanged in hypervitaminosis A. These data indicate that the rate of intracellular protein degradation is not determined by the level of "free cathepsins. Protein synthesis in the livers of the hypervitaminotic animals was partially imparied, as shown by the shift of polysomal profiles toward lighter aggregates.

Amino Acids↗

The state of messenger ribonucleic acid and ribosomes in the cytoplasm of ethionine-treated rat liver.

The administration of ethionine to female rats causes breakdown of hepatic polysomes. The state of mRNA and monomeric ribosomes after the polysome dissociation was studied. The mRNA was selectively labeled with [14C] orotate after a low dose of actinomycin D. Sucrose density gradient centrifugation of Triton X-100-treated cytoplasm revealed an accumulation of heterodisperse radioactive material with very large S values. This material was converted to smaller S values with deoxycholate treatment and was extremely sensitive to mild ribonuclease treatment. Since this material was banded at around 1.43 g/cm3 in CsCl gradient centrifugation and contained RNA with a distribution of S values characteristic of polysomal mRNA, this material was identified as mRNA-containing ribonucleoprotein particles. The monomeric ribosomes were shown to be dissociated into subunits in the presence of 0.5 M KCl, indicating that these lacked nascent polypeptide chains. When the animals were recovered from the ethionine treatment by subsequent administration of adenine and methionine, the heterodisperse ribonucleoprotein particles and monomeric ribosomes appeared to be utilized for the reformation of polysomes.

Animals↗