Literature DB >> 12947417

Condensed chromatin domains in the mammalian nucleus are accessible to large macromolecules.

Pernette J Verschure1, Ineke van der Kraan, Erik M M Manders, Deborah Hoogstraten, Adriaan B Houtsmuller, Roel van Driel.   

Abstract

Most chromatin in interphase nuclei is part of condensed chromatin domains. Previous work has indicated that transcription takes place primarily at the surface of chromatin domains, that is, in the perichromatin region. It is possible that genes inside chromatin domains are silenced due to inaccessibility to macromolecular components of the transcription machinery. We have tested the accessibility of chromatin domains in nuclei of living cells with proteins and dextrans of different molecular sizes. Our results show that chromatin domains are readily accessible to large macromolecules, including proteins with a molecular weight of several hundred kilodaltons. Therefore, the silencing of genes that are incorporated into such domains is not due to the physical inaccessibility of condensed chromatin domains to transcription factors.

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Year:  2003        PMID: 12947417      PMCID: PMC1326359          DOI: 10.1038/sj.embor.embor922

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


  29 in total

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Review 2.  DNA replication and nuclear architecture.

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Review 3.  Gene silencing, cell fate and nuclear organisation.

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5.  Action of DNA repair endonuclease ERCC1/XPF in living cells.

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6.  Rapid switching of TFIIH between RNA polymerase I and II transcription and DNA repair in vivo.

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8.  Localization of newly-synthesized DNA in a mammalian cell as visualized by high resolution autoradiography.

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Review 9.  Compartmentalization of eukaryotic gene expression: causes and effects.

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  42 in total

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3.  Evidence for short-range helical order in the 30-nm chromatin fibers of erythrocyte nuclei.

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4.  Dissecting chromatin interactions in living cells from protein mobility maps.

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Review 5.  Chromatin higher-order structure and dynamics.

Authors:  Christopher L Woodcock; Rajarshi P Ghosh
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Review 6.  Gene positioning.

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7.  Nuclear proteins: finding and binding target sites in chromatin.

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8.  Automated line scan analysis to quantify biosensor activity at the cell edge.

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9.  Mechanism of mRNA transport in the nucleus.

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10.  A glue for heterochromatin maintenance: stable SUV39H1 binding to heterochromatin is reinforced by the SET domain.

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