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Cited by 1,129

The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

ALTERATION OF NUCLEOSOME STRUCTURE AS A MECHANISM OF TRANSCRIPTIONAL REGULATION

Workman, J. L., Kingston, R. E.·1998·Annual Review of Biochemistry

Abstract

The nucleosome, which is the primary building block of chromatin, is not a static structure: It can adopt alternative conformations. Changes in solution conditions or changes in histone acetylation state cause nucleosomes and nucleosomal arrays to behave with altered biophysical properties. Distinct subpopulations of nucleosomes isolated from cells have chromatographic properties and nuclease sensitivity different from those of bulk nucleosomes. Recently, proteins that were initially identified as necessary for transcriptional regulation have been shown to alter nucleosomal structure. These proteins are found in three types of multiprotein complexes that can acetylate nucleosomes, deacetylate nucleosomes, or alter nucleosome structure in an ATP-dependent manner. The direct modification of nucleosome structure by these complexes is likely to play a central role in appropriate regulation of eukaryotic genes.

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Metadata

Authors
Workman, J. L., & Kingston, R. E.
Venue
Annual Review of Biochemistry
Published
1998-06
Volume
67
Issue
1
Pages
545-579
ISSN
  • 0066-4154 (ISSN-L)
  • 1545-4509
OpenAlex
W2132440338
Cited by
1,129
References
11
FWCI
6.69
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: ALTERATION OF NUCLEOSOME STRUCTURE AS A MECHANISM OF TRANSCRIPTIONAL REGULATION. https://app.cochat.ai/papers/10.1146/annurev.biochem.67.1.545
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Workman, J. L., & Kingston, R. E. (1998). ALTERATION OF NUCLEOSOME STRUCTURE AS A MECHANISM OF TRANSCRIPTIONAL REGULATION. Annual Review of Biochemistry. https://doi.org/10.1146/annurev.biochem.67.1.545

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.