All nuclear RNA synthesis is repressed during the mitotic phase of the cell cycle. In addition, RNA polymerase II (RNAP II), nascent RNA and many transcription factors disengage from DNA during mitosis. It has been proposed that mitotic transcription repression and disengagement of factors are due to either mitotic chromatin condensation or biochemical modifications to the transcription machinery. In this study, we investigate the requirement for chromatin condensation in establishing mitotic transcription repression and factor loss, by analyzing transcription and RNAP II localization in mitotic cells infected with herpes simplex virus type 1. We find that virus-infected cells enter mitosis and that mitotic viral DNA is maintained in a nucleosome-free and noncondensed state. Our data show that RNAP II transcription is repressed on cellular genes that are condensed into mitotic chromosomes and on viral genes that remain nucleosome free and noncondensed. Although RNAP II may interact indirectly with viral DNA during mitosis, it remains transcriptionally unengaged. This study demonstrates that mitotic repression of transcription and loss of transcription factors from mitotic DNA can occur independently of nucleosomal chromatin condensation.
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10 July 2000
Article|
July 10 2000
Mitotic Transcription Repression in Vivo in the Absence of Nucleosomal Chromatin Condensation
Charlotte A. Spencer,
Charlotte A. Spencer
aDepartment of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, Alberta, Canada T6G 1Z2
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Michael J. Kruhlak,
Michael J. Kruhlak
bDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, Alberta, Canada T2N 4N1
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Heather L. Jenkins,
Heather L. Jenkins
aDepartment of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, Alberta, Canada T6G 1Z2
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Xuejun Sun,
Xuejun Sun
aDepartment of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, Alberta, Canada T6G 1Z2
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David P. Bazett-Jones
David P. Bazett-Jones
bDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, Alberta, Canada T2N 4N1
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Charlotte A. Spencer
aDepartment of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, Alberta, Canada T6G 1Z2
Michael J. Kruhlak
bDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, Alberta, Canada T2N 4N1
Heather L. Jenkins
aDepartment of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, Alberta, Canada T6G 1Z2
Xuejun Sun
aDepartment of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, Alberta, Canada T6G 1Z2
David P. Bazett-Jones
bDepartment of Cell Biology and Anatomy, University of Calgary, Calgary, Alberta, Canada T2N 4N1
The online version of this article contains supplemental material.
Abbreviations used in this paper: 3-D, three-dimensional; DAPI, 4′,6-diamidine-2-phenylindole; ESI, electron spectroscopic imaging; HSV-1, herpes simplex virus type 1; MOI, multiplicity of infection; RNAP, RNA polymerase.
Received:
February 07 2000
Revision Requested:
May 04 2000
Accepted:
May 25 2000
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 2000 The Rockefeller University Press
2000
The Rockefeller University Press
J Cell Biol (2000) 150 (1): 13–26.
Article history
Received:
February 07 2000
Revision Requested:
May 04 2000
Accepted:
May 25 2000
Citation
Charlotte A. Spencer, Michael J. Kruhlak, Heather L. Jenkins, Xuejun Sun, David P. Bazett-Jones; Mitotic Transcription Repression in Vivo in the Absence of Nucleosomal Chromatin Condensation. J Cell Biol 10 July 2000; 150 (1): 13–26. doi: https://doi.org/10.1083/jcb.150.1.13
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