Literature DB >> 6197951

Non-random effect on RNA synthesis in liver chromatin by administration of dimethylnitrosamine to mice.

M Klaude, A von der Decken.   

Abstract

The effect of dimethylnitrosamine on functional activities of liver chromatin was studied in mice. After a single dose of dimethylnitrosamine injected i.v. (25 mg/kg body wt, 45 min before sacrifice) liver nuclei were isolated and incubated with micrococcal nuclease (EC 3.1.4.7) to an acid-solubility of 2.5% of total DNA. Chromatin was fractionated into a 1,200 g pellet P1, 102,000 g pellet P2 and supernatant fraction S2. Chromatin-bound RNA polymerase I plus III activity decreased 15% in the P1 and 25% in the P2 fraction. No changes in activity were observed in the S2 fraction. Chromatin-bound RNA polymerase II activity decreased 19% in the P1, 49% in the P2 and 32% in the S2 fraction. Heparin stimulated RNA polymerase II activity decreased 10% in the P1 and 44% in the P2 fraction. Formation of initiation in nuclear lysates with RNA polymerase from Escherichia coli increased after administration of dimethylnitrosamine suggesting an increase in the number of sites available for the start of new RNA chains. The results show that limited digestion of nuclei with endonuclease cleaves chromatin regions which are more affected by dimethylnitrosamine than the total chromatin suggesting a non-random effect of the hepatotoxin on chromatin. Modifications of the DNA template by dimethylnitrosamine is indicated by the change in number of initiation complexes.

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Year:  1983        PMID: 6197951     DOI: 10.1007/bf01239205

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  30 in total

1.  An improved method for the quantitative isolation of rat liver nuclear RNA polymerases.

Authors:  F L Yu
Journal:  Biochim Biophys Acta       Date:  1975-07-07

2.  The mechanism by which heparin stimulates transcription in isolated rat liver nuclei. Polyribonucleotide elongation rates and the number of transcribing RNA polymerase molecules present.

Authors:  B E Coupar; C J Chesterton
Journal:  Eur J Biochem       Date:  1977-10-03

3.  Two functional states of the RNA polymerases in the rat hepatic nuclear and nucleolar fractions.

Authors:  F L Yu
Journal:  Nature       Date:  1974-09-27       Impact factor: 49.962

4.  Initiation by the DNA-dependent RNA polymerase.

Authors:  D D Anthony; E Zeszotek; D A Goldthwait
Journal:  Proc Natl Acad Sci U S A       Date:  1966-09       Impact factor: 11.205

5.  Fractionation of hen oviduct chromatin into transcriptionally active and inactive regions after selective micrococcal nuclease digestion.

Authors:  K S Bloom; J N Anderson
Journal:  Cell       Date:  1978-09       Impact factor: 41.582

6.  Quantification of hepatic transcribing RNA polymerase molecules, polyribonucleotide elongation rates and messenger RNA complexity in fed and fasted rats.

Authors:  B E Coupar; J A Davies; C J Chesterton
Journal:  Eur J Biochem       Date:  1978-03-15

7.  Control of transcription and translation by low molecular weight peptides (deprimerones) from chromatin and poly(A)-messenger RNA. Implication in the mechanism of carcinogenesis.

Authors:  M Hillar; J Przyjemski
Journal:  Biochim Biophys Acta       Date:  1979-09-27

8.  The stability of methyl and ethyl phosphotriesters in DNA in vivo.

Authors:  K V Shooter; T A Slade
Journal:  Chem Biol Interact       Date:  1977-12       Impact factor: 5.192

9.  Reduced transcription activity of rat liver chromatin after protein restriction and selective digestion of nuclei with micrococcus nuclease.

Authors:  S Aström; E K Arrhenius; A von der Decken
Journal:  J Nutr       Date:  1981-07       Impact factor: 4.798

10.  Effect of a single dose of dimethylnitrosamine on biosynthesis of nucleic acid and protein in rat liver and kidney.

Authors:  B W Stewart; P N Magee
Journal:  Biochem J       Date:  1971-12       Impact factor: 3.857

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