Literature DB >> 566162

Changes of nucleosome frequency in nucleolar and non-nucleolar chromatin as a function of transcription: an electron microscopic study.

U Scheer.   

Abstract

The morphology of nucleolar and non-nucleolar (lampbrush chromosome loops) chromatin was studied in the electron microscope during states of reduced transcriptional activity in amphibian oocytes (Xenopus laevis, Triturus alpestris, T. cristatus). Reduced transcriptional activity was observed in maturing stages of oocyte development and after treatment with an inhibitor, actinomycin D. Strands of nucleolar chromatin appear smooth and thin, and contain only few, if any, nucleosomal particles in the transcribed units. This is true whether they are densely or only sparsely covered with lateral ribonucleoprotein fibrils. This smooth and non-nucleosomal character is also predominant in the interspersed, apparently nontranscribed rDNA spacer regions. During inactivation, however, nucleolar chromatin frequently and progressively assumes a beaded appearance in extended fibril-free--that is, apparently nontranscribed--regions. In either full-grown oocytes or late after drug treatment, most of the nucleolar chromatin is no longer smooth and thin, but rather shows a beaded configuration indistinguishable from inactive non-nucleolar chromatin. In many chromatin strands, transitions of fibril-associated regions of smooth character into beaded regions without lateral fibrils are seen. Similarly, in the non-nucleolar chromatin of the retracting lampbrush chromosome loops, reduced transcriptional activity is correlated with a change from smooth to beaded morphology. Here, however, beaded regions are also commonly found interspersed between the more or less distant bases of the lateral fibrils, the putative transcriptional complexes. In both sorts of chromatin, detergents (in particular Sarkosyl) that remove most of the chromatin proteins including histones from the DNA axis but leave the RNA polymerases of the transcriptional complexes attached were used to discriminate between polymerases and nucleosomal particles. The results suggest that nucleosomes are absent in heavily transcribed chromatin regions but are reformed after inactivation. In contrast to the findings with inactivated nucleolar genes, in lampbrush chromosome loops the beaded nucleosomal configuration appears to be assumed also in regions within transcriptional units that, perhaps temporarily, are not involved in transcription.

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Year:  1978        PMID: 566162     DOI: 10.1016/0092-8674(78)90327-6

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  44 in total

Review 1.  Survey and summary: transcription by RNA polymerases I and III.

Authors:  M R Paule; R J White
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

Review 2.  Lampbrush chromosomes and associated bodies: new insights into principles of nuclear structure and function.

Authors:  Garry T Morgan
Journal:  Chromosome Res       Date:  2002       Impact factor: 5.239

3.  Mitotic repression of RNA polymerase II transcription is accompanied by release of transcription elongation complexes.

Authors:  G G Parsons; C A Spencer
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

4.  Nucleosome rearrangement in human chromatin during UV-induced DNA- reapir synthesis.

Authors:  M J Smerdon; M W Lieberman
Journal:  Proc Natl Acad Sci U S A       Date:  1978-09       Impact factor: 11.205

5.  Transcription patterns of amplified Dytiscus genes coding for ribosomal RNA after injection into Xenopus oocyte nuclei.

Authors:  M F Trendelenburg; H Zentgraf; W W Franke; J B Gurdon
Journal:  Proc Natl Acad Sci U S A       Date:  1978-08       Impact factor: 11.205

6.  Transcription of adenovirus 2 major late and peptide IX genes under conditions of in vitro nucleosome assembly.

Authors:  T Matsui
Journal:  Mol Cell Biol       Date:  1987-04       Impact factor: 4.272

7.  Comparison on the structure and transcriptional capability of growing phase and stationary yeast chromatin: a model for reversible gene activation.

Authors:  D Lohr; G Ide
Journal:  Nucleic Acids Res       Date:  1979       Impact factor: 16.971

8.  Differences in the circular dichroism spectra of of eu- and heterochromatin fractions from rat liver.

Authors:  G H Moyer; E Kay; G E Austin
Journal:  Nucleic Acids Res       Date:  1979-04       Impact factor: 16.971

9.  Visualization of Transcription in early mouse embryos.

Authors:  M E Hughes; K Bürki; S Fakan
Journal:  Chromosoma       Date:  1979-08-10       Impact factor: 4.316

10.  RNA polymerase II pauses at the 5' end of the transcriptionally induced Drosophila hsp70 gene.

Authors:  T O'Brien; J T Lis
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

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