Skip Navigation

This Article
Right arrow Print PDF (2623K)
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 (49)
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Plumb, M.
Right arrow Articles by Stein, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Plumb, M.
Right arrow Articles by Stein, G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1983, Vol. 11, No. 22 7927-7945
© 1983


MOLECULAR BIOLOGY

Influence of DNA synthesis inhibition on the coordinate expression of core human hlstone genes during S phase

M. Plumb*, J. Stein+ and G. Stein*

*Department of Biochemistry and Molecular Biology Gainesville, FL 32610, USA +Department of Immunology and Medical Microbiology, University of Florida College of Medicine Gainesville, FL 32610, USA

Received July 18, 1983. Revised October 20, 1983. Accepted October 20, 1983.

Core hlstone mRNA metabolism has been examined 1n S phase HeLa cells recovering from UNA synthesis Inhibition by 1 mM hydroxyurea. Using cloned human hlstone genes as probes for hlstone mRNA quantitation, the response to and recovery from DNA synthesis Inhibition 1s shown to depend on the position of the cell with respect to the initiation of DNA replication. The incorporation of 3H-uridine Into multiple hlstone mRNAs in recovering cells does not exceed preinhibition levels, and as this Incorporation 1s maximal 1n early S phase, the synthesis of core hi stone mRNA is apparently related to the ordered replication of the genome. The total hlstone mRNA present in Interrupted S phase cells after recovery is not significantly different from that present in control cells, and a temporal and functional coupling between hi stone mRNA levels and the relative rate of DNA synthesis 1s maintained 1n perturbed cells.


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
W. F. Holmes, C. D. Braastad, P. Mitra, C. Hampe, D. Doenecke, W. Albig, J. L. Stein, A. J. van Wijnen, and G. S. Stein
Coordinate Control and Selective Expression of the Full Complement of Replication-dependent Histone H4 Genes in Normal and Cancer Cells
J. Biol. Chem., November 11, 2005; 280(45): 37400 - 37407.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
M. P. Markey, S. P. Angus, M. W. Strobeck, S. L. Williams, R. W. Gunawardena, B. J. Aronow, and E. S. Knudsen
Unbiased Analysis of RB-mediated Transcriptional Repression Identifies Novel Targets and Distinctions from E2F Action
Cancer Res., November 15, 2002; 62(22): 6587 - 6597.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
Z. Li and G. Childs
Temporal Activation of the Sea Urchin Late H1 Gene Requires Stage-Specific Phosphorylation of the Embryonic Transcription Factor SSAP
Mol. Cell. Biol., May 1, 1999; 19(5): 3684 - 3695.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
L Dailey, S B Roberts, and N Heintz
Purification of the human histone H4 gene-specific transcription factors H4TF-1 and H4TF-2.
Genes & Dev., December 1, 1988; 2(12b): 1700 - 1712.
[Abstract] [PDF]


Home page
ScienceHome page
E. O'Neill, C Fletcher, C. Burrow, N Heintz, R. Roeder, and T. Kelly
Transcription factor OTF-1 is functionally identical to the DNA replication factor NF-III
Science, September 2, 1988; 241(4870): 1210 - 1213.
[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.