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PMID: 2901725 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Identification of DNA sequences required for mouse APRT gene expression.

Nucleic acids research ·Vol. 16 ·No. 17 ·1988-09-12 ·Pages 8509-24

Dush MK, Briggs MR, Royce ME, Schaff DA, Khan SA, Tischfield JA, Stambrook PJ

Abstract

The mouse aprt promoter contains four GC boxes, which bind transcription factor Spl in vitro, and lacks both TATA and CCAAT boxes. Removal of the two most distal GC boxes of this promoter had little effect on APRT enzyme levels produced in a transient expression assay. Deletion of the distal three GC boxes resulted in a 50% reduction, and deletion of all GC boxes resulted in essentially complete loss of APRT activity. There are two predominant transcription start sites which are located within the region containing the GC boxes. The promoter behaved as a relatively strong promoter when compared to the RSV LTR promoter in a transient CAT assay, and operated in one orientation only. No upstream anti-sense transcripts were detected in either mouse CAK or liver cells, confirming that the mouse aprt promoter, unlike some other GC-rich promoters appears not to support bidirectional transcription.

MeSH Terms
Adenine Phosphoribosyltransferase/genetics,metabolism Animals Base Sequence Cell Line Chromosome Deletion Genes Genes, Homeobox Kinetics Mice Molecular Sequence Data Mutation Pentosyltransferases/genetics Plasmids Promoter Regions, Genetic Transcription, Genetic Transfection
Chemicals
Pentosyltransferases Adenine Phosphoribosyltransferase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Dush M K
Department of Anatomy and Cell Biology, University of Cincinnati College of Medicine, OH 45267.
Briggs M R
Royce M E
Schaff D A
Khan S A
Tischfield J A
Stambrook P J
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1988-09-12
Pages
8509-24
Language
English
Region
England
NLM ID
0411011
PMCID
PMC338573
Subset
IM
Grants
NCI NIH HHS · CA 36897 · United States
NIDDK NIH HHS · DK 38185 · United States
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