Skip Navigation

This Article
Right arrow Print PDF (4877K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (114)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Weisbrod, S. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Weisbrod, S. T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1982, Vol. 10, No. 6 2017-2042
© 1982


MOLECULAR BIOLOGY

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

Stuart T. Weisbrod*

Laboratory of Molecular Biology, Medical Research Council Centre Hills Road, Cambridge CB2 2QH, UK

Received December 1, 1981. Revised February 10, 1982. Accepted February 22, 1982.

Nucleosomes fran actively transcribed genes (active nucleosomes) contain nonhistone proteins HMG 14 and 17 and are preferentially sensitive to digestion by DNAse I. Active nucleosomes isolated by chromatography on an HMG 14 and 17 glass bead affinity column were analyzed with respect to overall structure, accessory nonhistone components and modifications to the ENA and histones. the experiments lead to the following conclusions: The DNR in the active nucleosome is undermethylated compared to bulk DNA; topoisomerase I is a non-stoichiometric component of the active nucleosomes fraction; the level of histone acetylation is enriched in active nucleosames, but the extent of enrichment cannot account for HMG binding; and the two histone H3 molecules in the active nucleosome can dimerize more readily and are, therefore, probably closer together than those in the bulk of the nucleosomes. Additionally it is shown that HMG 14 and 17 prefer to bind to single- vs. double-stranded nucleic acids. The role of HMG 14 and 17 in producing a highly DNAse I sensitive structure and correspondingly helping to facilitate transcription is discussed in terms of these properties.


*Present address: Cold Spring Harbor Laboratory, P.O. Box 100, Cold Spring Harbor, NY 11724, USA


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
D. A. Hill, C. L. Peterson, and A. N. Imbalzano
Effects of HMGN1 on Chromatin Structure and SWI/SNF-mediated Chromatin Remodeling
J. Biol. Chem., December 16, 2005; 280(50): 41777 - 41783.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. Yu, E. Khan, M. A. Khaleque, J. Lee, G. Laco, G. Kohlhagen, S. Kharbanda, Y.-C. Cheng, Y. Pommier, and A. Bharti
Phosphorylation of DNA Topoisomerase I by the c-Abl Tyrosine Kinase Confers Camptothecin Sensitivity
J. Biol. Chem., December 10, 2004; 279(50): 51851 - 51861.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. R. Kramer, G. Fragoso, W. Pennie, H. Htun, G. L. Hager, and R. R. Sinden
Transcriptional State of the Mouse Mammary Tumor Virus Promoter Can Affect Topological Domain Size in Vivo
J. Biol. Chem., October 1, 1999; 274(40): 28590 - 28597.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
F. Carrier, P. T. Georgel, P. Pourquier, M. Blake, H. U. Kontny, M. J. Antinore, M. Gariboldi, T. G. Myers, J. N. Weinstein, Y. Pommier, et al.
Gadd45, a p53-Responsive Stress Protein, Modifies DNA Accessibility on Damaged Chromatin
Mol. Cell. Biol., March 1, 1999; 19(3): 1673 - 1685.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
B M Shykind, J Kim, L Stewart, J J Champoux, and P A Sharp
Topoisomerase I enhances TFIID-TFIIA complex assembly during activation of transcription.
Genes & Dev., February 1, 1997; 11(3): 397 - 407.
[Abstract] [PDF]


Home page
Cold Spring Harb Symp Quant BiolHome page
A. Varshavsky, L. Levinger, O. Sundin, J. Barsoum, E. Ozkaynak, P. Swerdlow, and D. Finley
Cellular and SV40 Chromatin: Replication, Segregation, Ubiqiritination, Nuclease-hypersensitive Sites, HMG-containing Nueleosomes, and Heterochromatin-specific Protein
Cold Spring Harb Symp Quant Biol, January 1, 1983; 47(0): 511 - 528.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.