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(Received for publication, May 28, 1996, and in revised form, July 15, 1996)
From the A purine/pyrimidine mirror repeat element
(M-PMR3) in the MUC1 promoter has been shown to form H-DNA
under in vitro conditions. We investigated this element for
biological function in the regulation of transcription of this
gene. Chloramphenicol acetyltransferase reporter-promoter
constructs were prepared in which the mirror repeat element (PMR3) was
intact, deleted, or modified, and their activities were evaluated by
transient transfection assays into the cell lines Capan-2, PANC1, and
HT-29. Deletion or modification of M-PMR3 increased expression of
chloramphenicol acetyltransferase activity in
MUC1-expressing cells; however, a role for an H-DNA
structure in this activity was not supported by the results.
Volume 271, Number 43,
Issue of October 25, 1996
pp. 26543-26546
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
,
§
and
Eppley Institute for Research in Cancer and
Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska
68198-6805 and the § Department of Biochemistry and
Molecular Biology, Mayo Foundation, Rochester, Minnesota 55905
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