Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Min-Hye Jeong is active.

Publication


Featured researches published by Min-Hye Jeong.


PLOS ONE | 2013

Agrobacterium tumefaciens -Mediated Transformation of the Lichen Fungus, Umbilicaria muehlenbergii

Sook-Young Park; Min-Hye Jeong; Hai-Ying Wang; Jung A Kim; Nan-Hee Yu; Sungbeom Kim; Yong Hwa Cheong; Seogchan Kang; Yong-Hwan Lee; Jae-Seoun Hur

Transformation-mediated mutagenesis in both targeted and random manners has been widely applied to decipher gene function in diverse fungi. However, a transformation system has not yet been established for lichen fungi, severely limiting our ability to study their biology and mechanism underpinning symbiosis via gene manipulation. Here, we report the first successful transformation of the lichen fungus, Umbilicaria muehlenbergii, via the use of Agrobacterium tumefaciens. We generated a total of 918 transformants employing a binary vector that carries the hygromycin B phosphotransferase gene as a selection marker and the enhanced green fluorescent protein gene for labeling transformants. Randomly selected transformants appeared mitotically stable, based on their maintenance of hygromycin B resistance after five generations of growth without selection. Genomic Southern blot showed that 88% of 784 transformants contained a single T-DNA insert in their genome. A number of putative mutants affected in colony color, size, and/or morphology were found among these transformants, supporting the utility of Agrobacterium tumefaciens-mediated transformation (ATMT) for random insertional mutagenesis of U. muehlenbergii. This ATMT approach potentially offers a systematic gene functional study with genome sequences of U. muehlenbergii that is currently underway.


PLOS ONE | 2014

Lichen Secondary Metabolites in Flavocetraria cucullata Exhibit Anti-Cancer Effects on Human Cancer Cells through the Induction of Apoptosis and Suppression of Tumorigenic Potentials

Thanh Thi Nguyen; Somy Yoon; Yi Yang; Ho-Bin Lee; Soon-Ok Oh; Min-Hye Jeong; Jong-Jin Kim; Sung-Tae Yee; Florin Crişan; Cheol Moon; Kwang Youl Lee; Kyung Keun Kim; Jae-Seoun Hur; Hangun Kim

Lichens are symbiotic organisms which produce distinct secondary metabolic products. In the present study, we tested the cytotoxic activity of 17 lichen species against several human cancer cells and further investigated the molecular mechanisms underlying their anti-cancer activity. We found that among 17 lichens species, F. cucullata exhibited the most potent cytotoxicity in several human cancer cells. High performance liquid chromatography analysis revealed that the acetone extract of F. cucullata contains usnic acid, salazinic acid, Squamatic acid, Baeomycesic acid, d-protolichesterinic acid, and lichesterinic acid as subcomponents. MTT assay showed that cancer cell lines were more vulnerable to the cytotoxic effects of the extract than non-cancer cell lines. Furthermore, among the identified subcomponents, usnic acid treatment had a similar cytotoxic effect on cancer cell lines but with lower potency than the extract. At a lethal dose, treatment with the extract or with usnic acid greatly increased the apoptotic cell population and specifically activated the apoptotic signaling pathway; however, using sub-lethal doses, extract and usnic acid treatment decreased cancer cell motility and inhibited in vitro and in vivo tumorigenic potentials. In these cells, we observed significantly reduced levels of epithelial-mesenchymal transition (EMT) markers and phosphor-Akt, while phosphor-c-Jun and phosphor-ERK1/2 levels were only marginally affected. Overall, the anti-cancer activity of the extract is more potent than that of usnic acid alone. Taken together, F. cucullata and its subcomponent, usnic acid together with additional component, exert anti-cancer effects on human cancer cells through the induction of apoptosis and the inhibition of EMT.


PLOS ONE | 2016

Inhibitory Activity of (+)-Usnic Acid against Non-Small Cell Lung Cancer Cell Motility

Yi Yang; Thanh Thi Nguyen; Min-Hye Jeong; Florin Crişan; Young Hyun Yu; Hyung-Ho Ha; Kyung Hee Choi; Hye Gwang Jeong; Tae Cheon Jeong; Kwang Youl Lee; Kyung Keun Kim; Jae-Seoun Hur; Hangun Kim

Lichens are symbiotic organisms that produce various unique chemicals that can be used for pharmaceutical purposes. With the aim of screening new anti-cancer agents that inhibit cancer cell motility, we tested the inhibitory activity of seven lichen species collected from the Romanian Carpathian Mountains against migration and invasion of human lung cancer cells and further investigated the molecular mechanisms underlying their anti-metastatic activity. Among them, Alectoria samentosa, Flavocetraria nivalis, Alectoria ochroleuca, and Usnea florida showed significant inhibitory activity against motility of human lung cancer cells. HPLC results showed that usnic acid is the main compound in these lichens, and (+)-usnic acid showed similar inhibitory activity that crude extract have. Mechanistically, β-catenin-mediated TOPFLASH activity and KITENIN-mediated AP-1 activity were decreased by (+)-usnic acid treatment in a dose-dependent manner. The quantitative real-time PCR data showed that (+)-usnic acid decreased the mRNA level of CD44, Cyclin D1 and c-myc, which are the downstream target genes of both β-catenin/LEF and c-jun/AP-1. Also, Rac1 and RhoA activities were decreased by treatment with (+)-usnic acid. Interestingly, higher inhibitory activity for cell invasion was observed when cells were treated with (+)-usnic acid and cetuximab. These results implied that (+)-usnic acid might have potential activity in inhibition of cancer cell metastasis, and (+)-usnic acid could be used for anti-cancer therapy with a distinct mechanisms of action.


Polar Biology | 2014

Diversity of endophytic fungi associated with bryophyte in the maritime Antarctic (King George Island)

Nan Hee Yu; Jung A Kim; Min-Hye Jeong; Yong Hwa Cheong; Soon Gyu Hong; Jae Sung Jung; Young Jin Koh; Jae-Seoun Hur

Abstract Bryophytes comprise one of the richest microfungal microhabitats in the Antarctic environment. The maritime Antarctic is very vulnerable to rapid environmental change caused by global warming. The aim of this study was to investigate the importance of bryophytes as a microhabitat for fungal species in the maritime Antarctic by surveying endophytic fungal diversity from several bryophytes including Andreaea sp., Barbilophozia hatcheri, Chorisodontium aciphyllum, Polytrichum alpinum, Polytrichumstrictum, Sanionia uncinata, and Warnstorfia sarmentosa. We collected 13 bryophyte samples at four localities on Barton Peninsula, King George Island. In total, 31 endophytic fungi morphotypes were isolated from bryophyte tissues by a thorough surface sterilization method. Using internal transcribed spacer sequence analysis, 16 endophytic fungal strains belonging to Ascomycota (12), Basidiomycota (1), Oomycota (1), and Zygomycota (2) phyla were obtained. Our results suggest the presence of a diverse range of fungal species even in a very limited area, and those bryophytes play an important role in conserving fungal diversity in this harsh environment. Growth rate measurements at a wide range of temperatures confirmed that most of the fungal strains were both mesophilic and psychrotolerant. This is the first report of endophytic fungi in Antarctic moss tissue by fluorescence in situ hybridization.


Genome Announcements | 2014

Draft Genome Sequence of Lichen-Forming Fungus Cladonia metacorallifera Strain KoLRI002260

Sook-Young Park; Jae Young Choi; Gir-Won Lee; Jung A Kim; Soon-Ok Oh; Min-Hye Jeong; Nan-Hee Yu; Soonok Kim; Yong-Hwan Lee; Jae-Seoun Hur

ABSTRACT The lichen-forming fungus Cladonia metacorallifera strain KoLRI002260 is capable of producing a number of secondary metabolites, including usnic, didymic, and squamatic acids, which have antitumor, antioxidant, and antibiotic activities. The draft genome assembly has a size of 36,682,060 bp, with a G+C content of 44.91%, and consists of 30 scaffolds.


PLOS ONE | 2015

Lichen Secondary Metabolite, Physciosporin, Inhibits Lung Cancer Cell Motility.

Yi Yang; So-Yeon Park; Thanh Thi Nguyen; Young Hyun Yu; Tru Van Nguyen; Eun Gene Sun; Jayalal Udeni; Min-Hye Jeong; Iris Pereira; Cheol Moon; Hyung-Ho Ha; Kyung Keun Kim; Jae-Seoun Hur; Hangun Kim

Lichens produce various unique chemicals that can be used for pharmaceutical purposes. To screen for novel lichen secondary metabolites showing inhibitory activity against lung cancer cell motility, we tested acetone extracts of 13 lichen samples collected in Chile. Physciosporin, isolated from Pseudocyphellaria coriacea (Hook f. & Taylor) D.J. Galloway & P. James, was identified as an effective compound and showed significant inhibitory activity in migration and invasion assays against human lung cancer cells. Physciosporin treatment reduced both protein and mRNA levels of N-cadherin with concomitant decreases in the levels of epithelial-mesenchymal transition markers such as snail and twist. Physciosporin also suppressed KITENIN (KAI1 C-terminal interacting tetraspanin)-mediated AP-1 activity in both the absence and presence of epidermal growth factor stimulation. Quantitative real-time PCR analysis showed that the expression of the metastasis suppressor gene, KAI1, was increased while that of the metastasis enhancer gene, KITENIN, was dramatically decreased by physciosporin. Particularly, the activity of 3’-untranslated region of KITENIN was decreased by physciosporin. Moreover, Cdc42 and Rac1 activities were decreased by physciosporin. These results demonstrated that the lichen secondary metabolite, physciosporin, inhibits lung cancer cell motility through novel mechanisms of action.


Genome Announcements | 2014

Draft Genome Sequence of Umbilicaria muehlenbergii KoLRILF000956, a Lichen-Forming Fungus Amenable to Genetic Manipulation

Sook-Young Park; Jae Young Choi; Gir-Won Lee; Min-Hye Jeong; Jung A Kim; Soon-Ok Oh; Yong-Hwan Lee; Jae-Seoun Hur

ABSTRACT Umbilicaria muehlenbergii strain KoLRILF000956 is amenable to Agrobacterium tumefaciens-mediated transformation (ATMT), making it the only known genetically tractable lichen-forming fungus to date. We report another advancement in lichen genetics, a draft genome assembly for U. muehlenbergii with a size of 34,812,353 bp and a GC content of 47.12%, consisting of seven scaffolds.


Genome Announcements | 2013

Draft Genome Sequence of Cladonia macilenta KoLRI003786, a Lichen-Forming Fungus Producing Biruloquinone.

Sook-Young Park; Jae Young Choi; Jung A Kim; Min-Hye Jeong; Soonok Kim; Yong-Hwan Lee; Jae-Seoun Hur

ABSTRACT The lichen-forming fungus Cladonia macilenta strain KoLRI003786 is capable of producing an acetylcholinesterase inhibitor, biruloquinone, which effectively prevents neurodegeneration in Alzheimers disease. Laying the foundation to unravel the biruloquinone biosynthetic pathway, we present the 37.11-Mb draft genome sequence of strain KoLRI003786.


Journal of Natural Products | 2018

Bioactive α-Pyrone Derivatives from the Endolichenic Fungus Dothideomycetes sp. EL003334

Gil Soo Kim; Wonmin Ko; Jong Won Kim; Min-Hye Jeong; Sung-Kyun Ko; Jae-Seoun Hur; Hyuncheol Oh; Jae-Hyuk Jang; Jong Seog Ahn

Two new α-pyrones, dothideopyrones E (1) and F (2), were isolated from a culture of the endolichenic fungus Dothideomycetes sp. EL003334. Their structures were elucidated by spectroscopic data analysis. Their absolute configurations were established by the modified Moshers method. Compound 2 inhibited nitric oxide (NO) production with IC50 values of 15.0 ± 2.8 μM in lipopolysaccharide (LPS)-induced BV2 cells. Compound 2 diminished the protein expression levels of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). Additionally, 2 decreased the mRNA expression levels of pro-inflammatory cytokines, such as tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6.


The Journal of Antibiotics | 2018

Anti-inflammatory phomalichenones from an endolichenic fungus Phoma sp.

Jong Won Kim; Wonmin Ko; Eun Kim; Gil Soo Kim; Gwi Ja Hwang; Sangkeun Son; Min-Hye Jeong; Jae-Seoun Hur; Hyuncheol Oh; Sung-Kyun Ko; Jae-Hyuk Jang; Jong Seog Ahn

Four new compounds, phomalichenones A–D (1–4), and seven known compounds (5–11) were isolated from the cultures of an endolichenic fungus Phoma sp. EL002650. Their structures were determined by the analysis of their spectroscopic data (NMR and MS). Compounds 1 and 6 inhibited nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages. In addition, compound 1 diminished the protein expression levels of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), and decreased the mRNA expression levels of pro-inflammatory cytokines, such as tumor necrosis factor-α (TNF-α), interleukin(IL)-1β, and IL-6.

Collaboration


Dive into the Min-Hye Jeong's collaboration.

Top Co-Authors

Avatar

Jae-Seoun Hur

Sunchon National University

View shared research outputs
Top Co-Authors

Avatar

Jung A Kim

Sunchon National University

View shared research outputs
Top Co-Authors

Avatar

Anna S. Kondratiuk

Sunchon National University

View shared research outputs
Top Co-Authors

Avatar

Hangun Kim

Sunchon National University

View shared research outputs
Top Co-Authors

Avatar

Kyung Keun Kim

Chonnam National University

View shared research outputs
Top Co-Authors

Avatar

Sook-Young Park

Sunchon National University

View shared research outputs
Top Co-Authors

Avatar

Yi Yang

Sunchon National University

View shared research outputs
Top Co-Authors

Avatar

Yong-Hwan Lee

Seoul National University

View shared research outputs
Top Co-Authors

Avatar

Jae Young Choi

Seoul National University

View shared research outputs
Top Co-Authors

Avatar

Soon-Ok Oh

Sunchon National University

View shared research outputs
Researchain Logo
Decentralizing Knowledge