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Molecular and Cellular Biology, June 1999, p. 4065-4078, Vol. 19, No. 6
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Ku Antigen-DNA Conformation Determines the
Activation of DNA-Dependent Protein Kinase and DNA Sequence-Directed
Repression of Mouse Mammary Tumor Virus Transcription
Ward
Giffin,1
Wenrong
Gong,1
Caroline
Schild-Poulter,1 and
Robert
J. G.
Haché1,2,*
Departments of
Medicine1 and Biochemistry, Microbiology
and Immunology,2 The Loeb Health Research
Institute at the Ottawa Hospital, University of Ottawa, Ottawa,
Ontario, Canada
Received 30 September 1998/Returned for modification 5 February
1999/Accepted 15 March 1999
Mouse mammary tumor virus (MMTV) transcription is repressed by
DNA-dependent protein kinase (DNA-PK) through a DNA sequence element,
NRE1, in the viral long terminal repeat that is a sequence-specific DNA
binding site for the Ku antigen subunit of the kinase. While Ku is an
essential component of the active kinase, how the catalytic subunit of
DNA-PK (DNA-PKcs) is regulated through its association with
Ku is only beginning to be understood. We report that activation of
DNA-PKcs and the repression of MMTV transcription from NRE1 are dependent upon Ku conformation, the manipulation of DNA structure by Ku, and the contact of Ku80 with DNA. Truncation of one copy of the
overlapping direct repeat that comprises NRE1 abrogated the repression
of MMTV transcription by Ku-DNA-PKcs. Remarkably, the
truncated element was recognized by Ku-DNA-PKcs with
affinity similar to that of the full-length element but was unable to
promote the activation of DNA-PKcs. Analysis of
Ku-DNA-PKcs interactions with DNA ends, double- and
single-stranded forms of NRE1, and the truncated NRE1 element revealed
striking differences in Ku conformation that differentially affected
the recruitment of DNA-PKcs and the activation of kinase activity.
*
Corresponding author. Mailing address: The Loeb Health
Research Institute, 725 Parkdale Ave., Ottawa, Ontario, Canada K1Y 4K9.
Phone: (613) 798-5555, ext. 6283. Fax: (613) 761-5036. E-mail: rhache{at}lri.ca.
Molecular and Cellular Biology, June 1999, p. 4065-4078, Vol. 19, No. 6
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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