Topoisomerase 1 inhibits MYC promoter activity by inducing G-quadruplex formation

Author:

Keller Josephine Geertsen12,Hymøller Kirstine Mejlstrup1,Thorsager Maria Eriksen1,Hansen Noriko Y1,Erlandsen Jens Uldum1,Tesauro Cinzia1,Simonsen Anne Katrine W1,Andersen Anne Bech1,Vandsø Petersen Kamilla1,Holm Lise Lolle34,Stougaard Magnus25,Andresen Brage Storstein34ORCID,Kristensen Peter6,Frøhlich Rikke1,Knudsen Birgitta R1ORCID

Affiliation:

1. Department of Molecular Biology and Genetics, Aarhus University , 8000 Aarhus C , Denmark

2. Department of Clinical Medicine, Aarhus University , 8000 Aarhus C , Denmark

3. Department of Biochemistry and Molecular Biology, University of Southern Denmark , 5230 Odense M , Denmark

4. Villum Center for Bioanalytical Sciences, University of Southern Denmark , 5230 Odense M , Denmark

5. Department of Pathology, Aarhus University Hospital , 8000 Aarhus C , Denmark

6. Faculty of Engineering and Science, Department of Chemistry and Bioscience, Aalborg University , 9220 Aalborg , Denmark

Abstract

Abstract We have investigated the function of human topoisomerase 1 (TOP1) in regulation of G-quadruplex (G4) formation in the Pu27 region of the MYC P1 promoter. Pu27 is among the best characterized G4 forming sequences in the human genome and it is well known that promoter activity is inhibited upon G4 formation in this region. We found that TOP1 downregulation stimulated transcription from a promoter with wildtype Pu27 but not if the G4 motif in Pu27 was interrupted by mutation(s). The effect was not specific to the MYC promoter and similar results were obtained for the G4 forming promoter element WT21. The other major DNA topoisomerases with relaxation activity, topoisomerases 2α and β, on the other hand, did not affect G4 dependent promoter activity. The cellular studies were supported by in vitro investigations demonstrating a high affinity of TOP1 for wildtype Pu27 but not for mutant sequences unable to form G4. Moreover, TOP1 was able to induce G4 formation in Pu27 inserted in double stranded plasmid DNA in vitro. This is the first time TOP1 has been demonstrated capable of inducing G4 formation in double stranded DNA and of influencing G4 formation in cells.

Funder

Novo Nordisk Foundation

Independent Research Fund Denmark

Publisher

Oxford University Press (OUP)

Subject

Genetics

Reference50 articles.

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