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CUT&Tag技术揭示了结核分枝杆菌在应对氧化应激时非常规的G-四链体景观。

CUT&Tag reveals unconventional G-quadruplex landscape in Mycobacterium tuberculosis in response to oxidative stress.

作者信息

Maurizio Ilaria, Ruggiero Emanuela, Zanin Irene, Conflitti Marta, Nicoletto Giulia, Provvedi Roberta, Richter Sara N

机构信息

Department of Molecular Medicine, University of Padua, Padua, Italy.

Department of Biology, University of Padua, Padua, Italy.

出版信息

Nat Commun. 2025 Aug 6;16(1):7253. doi: 10.1038/s41467-025-62485-4.

DOI:10.1038/s41467-025-62485-4
PMID:40770179
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12328624/
Abstract

Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis, remains a global health threat due to increasing drug resistance and high mortality rates. To combat tuberculosis effectively, novel therapeutic targets are urgently needed. G-quadruplexes (G4s) represent promising candidates for this purpose. In this study, we successfully apply the cleavage under targets and tagmentation (CUT&Tag) technique for the first time in bacteria, mapping the G4 landscape in Mtb under standard and oxidative stress conditions, the latter mimicking the environment Mtb faces within macrophages. We validate the CUT&Tag protocol using an antibody against the RNA polymerase β-subunit, confirming its association with actively transcribed genes. Employing the anti-G4 antibody BG4, we discovered that Mtb G4s, unlike their eukaryotic counterparts, predominantly locate within gene coding sequences and consist of two-guanine tract motifs. Notably, oxidative stress increases G4 formation, correlating with reduced gene expression. Our findings provide the first evidence of G4 formation in Mtb cells and suggest their potential role in bacterial survival within macrophages. This study demonstrates the successful application of CUT&Tag in bacteria and unveils an unconventional G4 landscape in Mtb, offering new insights into bacterial stress response mechanisms and potential therapeutic targets.

摘要

结核分枝杆菌(Mtb)是结核病的病原体,由于耐药性增加和高死亡率,仍然是全球健康的一大威胁。为了有效对抗结核病,迫切需要新的治疗靶点。G-四链体(G4s)有望成为这样的靶点。在本研究中,我们首次在细菌中成功应用了靶向切割与转座酶标签法(CUT&Tag)技术,绘制了在标准条件和氧化应激条件下Mtb中的G4图谱,后者模拟了Mtb在巨噬细胞内面临的环境。我们使用抗RNA聚合酶β亚基的抗体验证了CUT&Tag方案,证实了其与活跃转录基因的关联。使用抗G4抗体BG4,我们发现Mtb中的G4与真核生物中的不同,主要位于基因编码序列内,由双鸟嘌呤链基序组成。值得注意的是,氧化应激会增加G4的形成,这与基因表达降低相关。我们的研究结果首次证明了Mtb细胞中G4的形成,并表明它们在巨噬细胞内细菌存活中的潜在作用。本研究证明了CUT&Tag在细菌中的成功应用,并揭示了Mtb中一种非常规的G4图谱,为细菌应激反应机制和潜在治疗靶点提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/a3d3fcc2596f/41467_2025_62485_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/f917488a85cd/41467_2025_62485_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/fd41c6809900/41467_2025_62485_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/f9707520ecf1/41467_2025_62485_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/e1acbf7a29a3/41467_2025_62485_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/a3d3fcc2596f/41467_2025_62485_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/f917488a85cd/41467_2025_62485_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/fd41c6809900/41467_2025_62485_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/f9707520ecf1/41467_2025_62485_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/e1acbf7a29a3/41467_2025_62485_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b05/12328624/a3d3fcc2596f/41467_2025_62485_Fig5_HTML.jpg

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