Identification and characterisation of G-quadruplex DNA-forming sequences in the Pseudomonas aeruginosa genome

被引:4
作者
Evans, Lindsay [1 ]
Kotar, Anita [2 ]
Valentini, Martina [3 ]
Filloux, Alain [3 ]
Jamshidi, Shirin [4 ]
Plavec, Janez [2 ]
Rahman, Khondaker Miraz [4 ]
Vilar, Ramon [1 ]
机构
[1] Imperial Coll London, Dept Chem, White City Campus, London W12 OBZ, England
[2] Natl Inst Chem, Slovenian NMR Ctr, Hajdrihova 19, Ljubljana 1000, Slovenia
[3] Imperial Coll London, MRC Ctr Mol Microbiol & Infect, Dept Life Sci, South Kensington Campus, London SW7 2AZ, England
[4] Kings Coll London, Inst Pharmaceut Sci, Franklin Wilkins Bldg,150 Stamford St, London SE1 9NH, England
来源
RSC CHEMICAL BIOLOGY | 2023年 / 4卷 / 01期
基金
英国工程与自然科学研究理事会; 瑞士国家科学基金会; 英国生物技术与生命科学研究理事会;
关键词
ANTIBIOTIC-RESISTANCE; REGULATORY ROLES; BETA-LACTAM; MOTIFS; GENE; WIDE; RADIODURANS; PROMOTERS; BACTERIA;
D O I
10.1039/d2cb00205a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A number of Gram-negative bacteria such as Pseudomonas aeruginosa are becoming resistant to front-line antibiotics. Consequently, there is a pressing need to find alternative bio-molecular targets for the development of new drugs. Since non-canonical DNA structures such as guanine-quadruplexes (G4s) have been implicated in regulating transcription, we were interested in determining whether there are putative quadruplex-forming sequences (PQS) in the genome of Pseudomonas aeruginosa. Using bioinformatic tools, we screened 36 genes potentially relevant to drug resistance for the presence of PQS and 10 of these were selected for biophysical characterisation (i.e. circular dichroism and thermal difference UV/Vis spectroscopy). These studies showed that three of these G-rich sequences (linked to murE, ftsB and mexC genes) form stable guanine-quadruplexes which were studied by NMR spectroscopy; detailed analysis of one of the sequences (mexC) confirmed that it adopts a two-quartet antiparallel quadruplex structure in the presence of K+ ions. We also show by FRET melting assays that small molecules can stabilise these three new G4 DNA structures under physiological conditions. These initial results could be of future interest in the development of new antibiotics with alternative bio-molecular targets which in turn would help tackle antimicrobial resistance.
引用
收藏
页码:94 / 100
页数:7
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