Literature DB >> 18485894

DNase I footprinting of the nucleosome in whole nuclei.

D Z Staynov1.   

Abstract

DNase I was used to footprint the 147 bp DNA fragment of the nucleosome in whole chicken erythrocyte nuclei. It was found that the higher-order structure imposes an additional protection on nucleosomes at sites close to the entry and exit points of the linker DNA, around the dyad axis (site S 0). The observed protection is extended up to 20 bp on either side of S 0. It is partial (approximately 50%) and most probably reflects a full protection of different regions in alternatively oriented nucleosomes. These are the same regions which interact with linker histones. The results strongly support the findings by simulation of DNase I digests of unlabelled oligonucleosome fragments in the 30 nm fibre that in all nucleosomes sites S -5 to S -3 and S +3 to S +5 ara on the outside of the fibre exposed to DNase I.

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Year:  2008        PMID: 18485894     DOI: 10.1016/j.bbrc.2008.05.024

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  2 in total

1.  Coupling transcription factor occupancy to nucleosome architecture with DNase-FLASH.

Authors:  Jeff Vierstra; Hao Wang; Sam John; Richard Sandstrom; John A Stamatoyannopoulos
Journal:  Nat Methods       Date:  2013-11-03       Impact factor: 28.547

2.  DNA of a circular minichromosome linearized by restriction enzymes or other reagents is resistant to further cleavage: an influence of chromatin topology on the accessibility of DNA.

Authors:  Sławomir Kumala; Yasmina Hadj-Sahraoui; Joanna Rzeszowska-Wolny; Ronald Hancock
Journal:  Nucleic Acids Res       Date:  2012-07-30       Impact factor: 16.971

  2 in total

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