Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3973
Title: Characterization of highly conserved G-quadruplex motifs as potential drug targets in Streptococcus pneumoniae
Authors: Mishra, Subodh Kumar
Jain, Neha
Shankar, Uma
Kumar, Amit
Keywords: antiinfective agent;guanine quadruplex;bacterial genome;circular dichroism;conserved sequence;drug effect;gel mobility shift assay;genetics;nucleotide sequence;pathogenicity;Streptococcus pneumoniae;thermodynamics;virulence;Anti-Bacterial Agents;Base Sequence;Circular Dichroism;Conserved Sequence;Electrophoretic Mobility Shift Assay;G-Quadruplexes;Genome, Bacterial;Streptococcus pneumoniae;Thermodynamics;Virulence
Issue Date: 2019
Publisher: Nature Publishing Group
Citation: Mishra, S. K., Jain, N., Shankar, U., Tawani, A., Sharma, T. K., & Kumar, A. (2019). Characterization of highly conserved G-quadruplex motifs as potential drug targets in streptococcus pneumoniae. Scientific Reports, 9(1) doi:10.1038/s41598-018-38400-x
Abstract: Several G-quadruplex forming motifs have been reported to be highly conserved in the regulatory regions of the genome of different organisms and influence various biological processes like DNA replication, recombination and gene expression. Here, we report the highly conserved and three potentially G-quadruplex forming motifs (SP-PGQs) in the essential genes (hsdS, recD, and pmrA) of the Streptococcus pneumoniae genome. These genes were previously observed to play a vital role in providing the virulence to the bacteria, by participating in the host-pathogen interaction, drug-efflux system and recombination- repair system. However, the presence and importance of highly conserved G-quadruplex motifs in these genes have not been previously recognized. We employed the CD spectroscopy, NMR spectroscopy, and electrophoretic mobility shift assay to confirm the adaptation of the G-quadruplex structure by the SP-PGQs. Further, ITC and CD melting analysis revealed the energetically favorable and thermodynamically stable interaction between a candidate G4 binding small molecule TMPyP4 and SP-PGQs. Next, TFP reporter based assay confirmed the regulatory role of SP-PGQs in the expression of PGQ harboring genes. All these experiments together characterized the SP-PGQs as a promising drug target site for combating the Streptococcus pneumoniae infection. © 2019, The Author(s).
URI: https://doi.org/10.1038/s41598-018-38400-x
https://dspace.iiti.ac.in/handle/123456789/3973
ISSN: 2045-2322
Type of Material: Journal Article
Appears in Collections:Department of Biosciences and Biomedical Engineering

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