Literature DB >> 710437

Degradation of the ribosomal genes by DNAse I in Physarum polycephalum.

J Stalder, T Seebeck, R Braun.   

Abstract

Treatment of nuclei from Physarum polycephalum with DNAse I leads to DNA fragments with a regular pattern of multiples of 10 nucleotides, when analyzed on gels under denaturing conditions as has been shown for other eukaryotes. Reports from Weintraub and Axel lead to the conclusion, that active genes are preferentially digested by DNAse I. When Physarum chromatin is degraded by DNAse I, the ribosomal genes are no longer available for hybridization with 19-S and 26-S rRNA and are thus preferentially destroyed. Degradation of chromatin from nuclei in mitosis, where no rRNA is synthesized and from nuclei in late G2 phase, where rRNA synthesis is maximal, leads to the same proportion of the ribosomal sequences being lost for hybridization. Therefore the preferential degradation of the ribosomal genes in Physarum by DNAse I probably does not reflect the actual momentary activity of these genes. This suggests that DNAse I treatment may distinguish between active chromatin and very strongly repressed chromatin.

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Year:  1978        PMID: 710437     DOI: 10.1111/j.1432-1033.1978.tb12616.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  12 in total

1.  Nuclear architecture, intranuclear DNA distribution, and nuclease digestion.

Authors:  C Nicolini; A Diaspro; L Vergani; M Bertolotto; P Germano
Journal:  Cell Biophys       Date:  1988-08

2.  Structure of plant nuclear and ribosomal DNA containing chromatin.

Authors:  B Leber; V Hemleben
Journal:  Nucleic Acids Res       Date:  1979-11-10       Impact factor: 16.971

3.  Properties of active nucleosomes as revealed by HMG 14 and 17 chromatography.

Authors:  S T Weisbrod
Journal:  Nucleic Acids Res       Date:  1982-03-25       Impact factor: 16.971

4.  Nuclease sensitivity of chromatin containing active genes: kinetic analyses utilizing continuous elution of digestion products from an ultrafiltration cell.

Authors:  K J Vavra; D S Pederson; M A Gorovsky
Journal:  Nucleic Acids Res       Date:  1981-11-11       Impact factor: 16.971

5.  Selective release of HMG nonhistone proteins during DNase digestion of Tetrahymena chromatin at different stages of the cell cycle.

Authors:  K Hamana; M Zama
Journal:  Nucleic Acids Res       Date:  1980-11-25       Impact factor: 16.971

6.  Accurate transcription of simian virus 40 chromatin in a HeLa cell extract.

Authors:  J N Brady; M Radonovich; N P Salzman
Journal:  J Virol       Date:  1982-12       Impact factor: 5.103

7.  DNase I sensitivity of ribosomal genes in isolated nucleosome core particles.

Authors:  C P Giri; M A Gorovsky
Journal:  Nucleic Acids Res       Date:  1980-01-11       Impact factor: 16.971

8.  Limited DNase I nicking as a probe of gene conformation.

Authors:  M Zasloff; R D Camerini-Otero
Journal:  Proc Natl Acad Sci U S A       Date:  1980-04       Impact factor: 11.205

9.  Accessibility of ribosomal genes to trimethyl psoralen in nuclei of Physarum polycephalum.

Authors:  H S Judelson; V M Vogt
Journal:  Mol Cell Biol       Date:  1982-03       Impact factor: 4.272

10.  Mouse hepatic metallothionein-I gene cleavage by micrococcal nuclease is enhanced after induction by cadmium.

Authors:  J Koropatnick; G Andrews; J D Duerksen; U Varshney; L Gedamu
Journal:  Nucleic Acids Res       Date:  1983-05-25       Impact factor: 16.971

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