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.
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http://dx.doi.org/10.1093/nar/16.17.8509 | DOI Listing |
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Department of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, District of Columbia, United States.
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August 2023
Department of Genetics, the Silberman Institute, the Hebrew University of Jerusalem, Givat Ram, Jerusalem 91904, Israel. Electronic address:
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View Article and Find Full Text PDFFASEB J
March 2021
Energenesis Biomedical Co. Ltd, Taipei, Taiwan.
Adenine phosphoribosyltransferase (APRT) is the key enzyme involved in purine salvage by the incorporation of adenine and phosphoribosyl pyrophosphate to provide adenylate nucleotides. To evaluate the role of APRT in the repair processes of cutaneous wounds in healthy skin and in diabetic patients, a diabetic mouse model (db/db) and age-matched wild-type mice were used. Moreover, the topical application of adenine was assessed.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
July 2018
Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4L8, Canada;
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View Article and Find Full Text PDFPLoS One
September 2017
Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
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