Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/429346
Title: Role of Escherichia coli UvrD helicase in resolving G quadruplex DNA structures
Researcher: Shukla, Kaustubh
Guide(s): Nagaraju, Ganesh
Keywords: Biochemistry and Molecular Biology
Biology and Biochemistry
Life Sciences
University: Indian Institute of Science Bangalore
Completed Date: 2021
Abstract: G-quadruplex (G4) secondary structures have been implicated in various biological processes, including gene expression, DNA replication and telomere maintenance. However, unresolved G4 structures impede replication progression which can lead to the generation of DNA double-strand breaks and genome instability. Helicases have been shown to resolve G4 structures to facilitate faithful duplication of the genome. Escherichia coli UvrD (EcUvrD) helicase plays a crucial role in nucleotide excision repair, mismatch repair and in the regulation of homologous recombination. Here, we demonstrate a novel role of E. coli and Neisseria gonorrhoeae UvrD in resolving G4 tetraplexes. EcUvrD and N. gonorrhoeae UvrD were proficient in unwinding previously characterized tetramolecular G4 structures. Notably, EcUvrD was equally efficient in resolving tetramolecular and bimolecular G4 DNA that were derived from the potential G4-forming sequences from the genome of E. coli. Interestingly, in addition to resolving intermolecular G4 structures, EcUvrD was robust in unwinding intramolecular G4 structures. These data for the first time provide evidence for the role of UvrD in the resolution of G4 structures, which has implications for the in vivo role of UvrD helicase in G4 DNA resolution and genome maintenance. newline
Pagination: 
URI: http://hdl.handle.net/10603/429346
Appears in Departments:Biochemistry

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02_prelim pages.pdf157.04 kBAdobe PDFView/Open
03_table of contents.pdf46.71 kBAdobe PDFView/Open
04_abstract.pdf123.65 kBAdobe PDFView/Open
05_chapter 1.pdf1.36 MBAdobe PDFView/Open
06_annexure.pdf13.67 MBAdobe PDFView/Open
80_recommendation.pdf2.57 MBAdobe PDFView/Open
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