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Journal of Virology, March 1999, p. 1990-1997, Vol. 73, No. 3
Department of Biochemistry and Molecular
Biology, University of North Dakota School of Medicine, Grand
Forks, North Dakota 58202
Received 16 September 1998/Accepted 30 November 1998
The goal of this study was to determine the minimal sequence within
the simian virus 40 (SV40) late promoter region, nucleotides (nt) 255 to 424, capable of phasing nucleosomes as measured by its ability to
confer the greatest endonuclease sensitivity on adjacent DNA sequences.
To identify the minimal sequence, a deletional analysis of the late
region was performed by utilizing a SV40 recombinant reporter system.
The reporter system consisted of a series of unique restriction sites
introduced into SV40 at nt 2666. The unique restriction sites allowed
the insertion of test sequences as well as measurement of conferred
endonuclease sensitivity. The results of the deletional analysis
demonstrated that constructs capable of conferring the greatest
nuclease sensitivities consistently included nt 255 to 280. The
activator protein 4 (AP-4) and GTIIC transcription factor binding
sequences lie within this region and were analyzed individually. Their
abilities to confer nuclease sensitivity upon the reporter nearly
matched that of the entire late domain. These results suggest that
transcription factors AP-4 and transcription-enhancing factor which
binds the GTIIC sequence are able to confer significant levels of
nuclease sensitivity and are likely involved in the formation of the
SV40 nucleosome-free region.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Chromatin Structure of the Simian Virus 40 Late
Promoter: a Deletional Analysis
*
Corresponding author. Mailing address: Department of
Biochemistry and Molecular Biology, University of North Dakota School of Medicine, Grand Forks, ND 58202. Phone: (701) 777-4708. Fax: (701)
777-2382. E-mail:
bmilavetz{at}mail.med.und.nodak.edu.
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