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Kwang-Woo Jung 3 Articles
Functional Characterization of DNA N‑Glycosylase Ogg1 and Ntg1 in DNA Damage Stress of Cryptococcus neoformans
Kwang-Woo Jung , Sunhak Kwon , Jong-Hyun Jung , Sangyong Lim , Yong-Sun Bahn
J. Microbiol. 2023;61(11):981-992.   Published online December 6, 2023
DOI: https://doi.org/10.1007/s12275-023-00092-y
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AbstractAbstract PDF
Reactive oxygen species induce DNA strand breaks and DNA oxidation. DNA oxidation leads to DNA mismatches, resulting in mutations in the genome if not properly repaired. Homologous recombination (HR) and non-homologous end-joining (NHEJ) are required for DNA strand breaks, whereas the base excision repair system mainly repairs oxidized DNAs, such as 8-oxoguanine and thymine glycol, by cleaving the glycosidic bond, inserting correct nucleotides, and sealing the gap. Our previous studies revealed that the Rad53-Bdr1 pathway mainly controls DNA strand breaks through the regulation of HRand NHEJ-related genes. However, the functional roles of genes involved in the base excision repair system remain elusive in Cryptococcus neoformans. In the present study, we identified OGG1 and NTG1 genes in the base excision repair system of C. neoformans, which are involved in DNA oxidation repair. The expression of OGG1 was induced in a Hog1-dependent manner under oxidative stress. On the other hand, the expression of NTG1 was strongly induced by DNA damage stress in a Rad53-independent manner. We demonstrated that the deletion of NTG1, but not OGG1, resulted in elevated susceptibility to DNA damage agents and oxidative stress inducers. Notably, the ntg1Δ mutant showed growth defects upon antifungal drug treatment. Although deletion of OGG1 or NTG1 did not increase mutation rates, the mutation profile of each ogg1Δ and ntg1Δ mutant was different from that of the wild-type strain. Taken together, we found that DNA N-glycosylase Ntg1 is required for oxidative DNA damage stress and antifungal drug resistance in C. neoformans.

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  • Fungal DNA damage repair: from model to driver of virulence and AMR
    Callum Parkin, Adam G. Bainbridge, Johannes Gregor Matthias Rack
    Bioscience Reports.2026;[Epub]     CrossRef
  • Mechanistic Insights into Wildlife Cancer and Conservation Strategies Under the One Health Framework
    Qiangqiang Wang, Xiaoxuan Feng, Yurun Su, Naiwen Zhang, Yevheniia Dudnyk, Hongxuan He
    Veterinary Sciences.2026; 13(8): 815.     CrossRef
A Signature-Tagged Mutagenesis (STM)-based murine-infectivity assay for Cryptococcus neoformans
Kwang-Woo Jung , Kyung-Tae Lee , Yong-Sun Bahn
J. Microbiol. 2020;58(10):823-831.   Published online September 29, 2020
DOI: https://doi.org/10.1007/s12275-020-0341-8
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  • 4 Download
  • 2 Web of Science
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AbstractAbstract PDF
Signature-tagged mutagenesis (STM) is a high-throughput genetic technique that can be used to investigate the function of genes by constructing a large number of mutant strains with unique DNA identification tags, pooling them, and screening them for a particular phenotypic trait. STM was first designed for the identification of genes that contribute to the virulence or infectivity of a pathogen in its host. Recently, this
method
has also been applied for the identification of mutants with specific phenotypes, such as antifungal drug resistance and proliferation. In the present study, we describe an STM
method
for the identification of genes contributing to the infectivity of Cryptococcus neoformans using a mutant library, in which each strain was tagged with a unique DNA sequence.

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  • Genome-wide phenotypic profiling of transcription factors and identification of novel targets to control the virulence of Vibrio vulnificus
    Dayoung Sung, Garam Choi, Minji Ahn, Hokyung Byun, Tae Young Kim, Hojun Lee, Zee-Won Lee, Ji Yong Park, Young Hyun Jung, Ho Jae Han, Sang Ho Choi
    Nucleic Acids Research.2025;[Epub]     CrossRef
  • Zinc-binding domain mediates pleiotropic functions of Yvh1 in Cryptococcus neoformans
    Jae-Hyung Jin, Myung Kyung Choi, Hyun-Soo Cho, Yong-Sun Bahn
    Journal of Microbiology.2021; 59(7): 658.     CrossRef
Microbial radiation-resistance mechanisms
Kwang-Woo Jung , Sangyong Lim , Yong-Sun Bahn
J. Microbiol. 2017;55(7):499-507.   Published online June 30, 2017
DOI: https://doi.org/10.1007/s12275-017-7242-5
  • 1,147 View
  • 3 Download
  • 53 Crossref
AbstractAbstract PDF
Organisms living in extreme environments have evolved a wide range of survival strategies by changing biochemical and physiological features depending on their biological niches. Interestingly, organisms exhibiting high radiation resistance have been discovered in the three domains of life (Bacteria, Archaea, and Eukarya), even though a naturally radiationintensive environment has not been found. To counteract the deleterious effects caused by radiation exposure, radiation- resistant organisms employ a series of defensive systems, such as changes in intracellular cation concentration, excellent DNA repair systems, and efficient enzymatic and non-enzymatic antioxidant systems. Here, we overview past and recent findings about radiation-resistance mechanisms in the three domains of life for potential usage of such radiationresistant microbes in the biotechnology industry.

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