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鉴定肺炎链球菌中高度保守的 G-四链体基序作为潜在的药物靶点。

Characterization of highly conserved G-quadruplex motifs as potential drug targets in Streptococcus pneumoniae.

机构信息

Discipline of Biosciences and Biomedical Engineering, Indian Institute of Technology Indore, Simrol, Indore, 453552, India.

Centre for Bio-design and Diagnostics, Translational Health Science and Technology Institute, Faridabad, Haryana, India.

出版信息

Sci Rep. 2019 Feb 11;9(1):1791. doi: 10.1038/s41598-018-38400-x.

DOI:10.1038/s41598-018-38400-x
PMID:30741996
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6370756/
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.

摘要

已经有报道称,在不同生物体基因组的调控区域存在多个高度保守的 G-四链体形成基序,这些基序影响着多种生物学过程,如 DNA 复制、重组和基因表达。在这里,我们报道了肺炎链球菌基因组中必需基因(hsdS、recD 和 pmrA)中高度保守的三个潜在 G-四链体形成基序(SP-PGQs)。这些基因先前被观察到在参与宿主-病原体相互作用、药物外排系统和重组-修复系统中对细菌的毒力起着至关重要的作用。然而,这些基因中高度保守的 G-四链体基序的存在和重要性以前尚未被认识到。我们采用 CD 光谱、NMR 光谱和电泳迁移率变动分析来证实 SP-PGQs 适应 G-四链体结构。此外,ITC 和 CD 熔融分析揭示了候选 G4 结合小分子 TMPyP4 与 SP-PGQs 之间具有能量有利和热力学稳定的相互作用。接下来,基于 TFP 报告基因的测定证实了 SP-PGQs 在含 PGQ 基因表达中的调节作用。所有这些实验共同表明,SP-PGQs 是对抗肺炎链球菌感染的有前途的药物靶标位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/ccaf1b52a4c6/41598_2018_38400_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/6c8e5d2919c2/41598_2018_38400_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/c60720bfaf6b/41598_2018_38400_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/ba714bf259de/41598_2018_38400_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/725b29ed5d6c/41598_2018_38400_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/00c9eb9df71c/41598_2018_38400_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/63d4d027a9d7/41598_2018_38400_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/ccaf1b52a4c6/41598_2018_38400_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/6c8e5d2919c2/41598_2018_38400_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/c60720bfaf6b/41598_2018_38400_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/ba714bf259de/41598_2018_38400_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/725b29ed5d6c/41598_2018_38400_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/00c9eb9df71c/41598_2018_38400_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/63d4d027a9d7/41598_2018_38400_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b45/6370756/ccaf1b52a4c6/41598_2018_38400_Fig7_HTML.jpg

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