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Jaehoon Kim

Korea Advanced Institute of Science and Technology · 生化学・遺伝学・分子生物学

研究室紹介

Professor Jaehoon Kim's research lab focuses on epigenetic regulation, particularly the molecular mechanisms of histone modifications and their roles in gene regulation and disease. The lab investigates the enzymatic activities and functional interactions of ubiquitin ligases and deubiquitinases, such as yRad6, yBre1, RNF40/RNF20, and hFBH1, in chromatin remodeling and DNA damage response. Using biochemical reconstitution, structural analysis, and computational modeling, the lab explores how post-translational modifications of histones—especially H2B ubiquitylation and H3K4 methylation—regulate chromatin dynamics and cellular identity. The lab also applies machine learning to enhance sensing technologies, particularly for low-concentration gas detection, demonstrating interdisciplinary innovation in both biology and data science.

epigeneticshistone modificationubiquitin ligasechromatin dynamicsmachine learning in sensing

Research Overview

Papers
140
Total Citations
8,744
Papers (5y)
34
Primary Field
生化学・遺伝学・分子生物学

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
34total
2021
2022
2023
2024
2025
Citations per year (5y)
360total
20212022202320242025

Selected Papers

15
1
Article|535 citations·2009
RAD6-Mediated Transcription-Coupled H2B Ubiquitylation Directly Stimulates H3K4 Methylation in Human Cells
Jaehoon Kim, Mohamed Guermah, Robert K. McGinty, Jung‐Shin Lee, Zhanyun Tang, Thomas A. Milne, Ali Shilatifard, Tom W. Muir, Robert G. Roeder
SJR Q1CellOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology
2
Article|318 citations·2005
The Human Homolog of Yeast BRE1 Functions as a Transcriptional Coactivator through Direct Activator Interactions
Jaehoon Kim, Sandra B. Hake, Robert G. Roeder
SJR Q1Molecular CellOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology
3
Article|286 citations·2010
The Human PAF1 Complex Acts in Chromatin Transcription Elongation Both Independently and Cooperatively with SII/TFIIS
Jaehoon Kim, Mohamed Guermah, Robert G. Roeder
SJR Q1CellOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology
4
Article|143 citations·2013
The n-SET Domain of Set1 Regulates H2B Ubiquitylation-Dependent H3K4 Methylation
Jaehoon Kim, Jung‐Ae Kim, Robert K. McGinty, Uyen Nguyen, Tom W. Muir, C. David Allis, Robert G. Roeder
SJR Q1Molecular CellOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology
5
Article|130 citations·2009
Direct Bre1-Paf1 Complex Interactions and RING Finger-independent Bre1-Rad6 Interactions Mediate Histone H2B Ubiquitylation in Yeast
Jaehoon Kim, Robert G. Roeder
SJR Q1Journal of Biological ChemistryOA

Recent yeast genetic studies have implicated the ubiquitin-conjugating enzyme and ubiquitin ligase functions of yRad6 and yBre1, respectively, in H2B ubiquitylation. However, there have been no corresponding biochemical analyses demonstrating intrinsic enzyme activities of yRad6 and yBre1 or related mechanistic details. Here, we describe a robust in vitro chromatin ubiquitylation assay that involves purified H2B ubiquitylation factors and natural nucleosomes. Our results indicate that yRad6 has

Molecular BiologyBiochemistry, Genetics and Molecular Biology
6
Article|80 citations·2024
The secreted protein Amuc_1409 from Akkermansia muciniphila improves gut health through intestinal stem cell regulation
E. S. Kang, Jaehoon Kim, Young Eun Kim, Hana Lee, Kwang Bo Jung, Dong‐Ho Chang, Youngjin Lee, Shinhye Park, Eun-Young Lee, Eun‐Ji Lee, Ho Bum Kang, Moon-Young Rhyoo
SJR Q1Nature CommunicationsOA

Akkermansia muciniphila has received great attention because of its beneficial roles in gut health by regulating gut immunity, promoting intestinal epithelial development, and improving barrier integrity. However, A. muciniphila-derived functional molecules regulating gut health are not well understood. Microbiome-secreted proteins act as key arbitrators of host-microbiome crosstalk through interactions with host cells in the gut and are important for understanding host-microbiome relationships.

Molecular BiologyBiochemistry, Genetics and Molecular Biology
7
Article|75 citations·2002
The Novel Human DNA Helicase hFBH1 Is an F-box Protein
Jaehoon Kim, Jeong‐Hoon Kim, Sung Hak Lee, Do‐Hyung Kim, Hoyoung Kang, Sung-Ho Bae, Zhen‐Qiang Pan, Yeon‐Soo Seo
SJR Q1Journal of Biological ChemistryOA

We have identified a novel DNA helicase in humans that belongs to members of the superfamily I helicase and found that it contains a well conserved F-box motif at its N terminus. We have named the enzyme hFBH1 (human F-box DNA helicase 1). Recombinant hFBH1, containing glutathione S-transferase at the N terminus, was expressed in Sf9 cells and purified. In this report, we show that hFBH1 exhibited DNA-dependent ATPase and DNA unwinding activities that displace duplex DNA in the 3' to 5' directio

Molecular BiologyBiochemistry, Genetics and Molecular Biology
8
Article|74 citations·2020
Finding Hidden Signals in Chemical Sensors Using Deep Learning
Soo‐Yeon Cho, Youhan Lee, Sangwon Lee, Hohyung Kang, Jaehoon Kim, Jaehoon Kim, Jung‐Hoon Choi, Jin Hwa Ryu, Heeeun Joo, Hee‐Tae Jung, Jihan Kim, Jihan Kim
SJR Q1Analytical Chemistry

Achieving high signal-to-noise ratio in chemical and biological sensors enables accurate detection of target analytes. Unfortunately, below the limit of detection (LOD), it becomes difficult to detect the presence of small amounts of analytes and extract useful information via any of the conventional methods. In this work, we examine the possibility of extracting “hidden signals” using deep neural network to enhance gas sensing below the LOD region. As a test case system, we conduct experiments

Biomedical EngineeringEngineering
9
Article|48 citations·2020
H2B ubiquitylation enhances H3K4 methylation activities of human KMT2 family complexes
Minjung Kwon, Kihyun Park, Kwangbeom Hyun, Jeong‐Heon Lee, Linjiao Zhou, Young‐Wook Cho, Kai Ge, David G. Skalnik, Tom W. Muir, Jaehoon Kim
SJR Q1Nucleic Acids ResearchOA

In mammalian cells, distinct H3K4 methylation states are created by deposition of methyl groups by multiple complexes of histone lysine methyltransferase 2 (KMT2) family proteins. For comprehensive analyses that directly compare the catalytic properties of all six human KMT2 complexes, we employed a biochemically defined system reconstituted with recombinant KMT2 core complexes (KMT2CoreCs) containing minimal components required for nucleosomal H3K4 methylation activity. We found that each KMT2C

Molecular BiologyBiochemistry, Genetics and Molecular Biology
10
Article|43 citations·2017
Binding to RNA regulates Set1 function
Pierre Luciano, Jongcheol Jeon, Abdessamad El-Kaoutari, Drice Challal, Amandine Bonnet, Mara Barucco, Tito Candelli, Frédéric Jourquin, Pascale Lesage, Jaehoon Kim, Domenico Libri, Vincent Géli
SJR Q1Cell DiscoveryOA

Abstract The Set1 family of histone H3 lysine 4 (H3K4) methyltransferases is highly conserved from yeast to human. Here we show that the Set1 complex (Set1C) directly binds RNA in vitro through the regions that comprise the double RNA recognition motifs (dRRM) and N-SET domain within Set1 and its subunit Spp1. To investigate the functional relevance of RNA binding, we performed UV RNA crosslinking (CRAC) for Set1 and RNA polymerase II in parallel with ChIP-seq experiments. Set1 binds nascent tra

Molecular BiologyBiochemistry, Genetics and Molecular Biology
11
Review|38 citations·2020
Epigenetic modification and a role for the E3 ligase RNF40 in cancer development and metastasis
Junjiang Fu, Li Liao, Kyathegowdanadoddi Srinivasa Balaji, Chunli Wei, Jaehoon Kim, Jiangzhou Peng
SJR Q1OncogeneOA

RNF40 (OMIM: 607700) is a really interesting new gene (RING) finger E3 ubiquitin ligase containing multiple coiled-coil domains and a C-terminal RING finger motif, which engage in protein-DNA and protein-protein interactions. RNF40 encodes a polypeptide of 1001 amino acids with a predicted molecular mass of 113,678 Da. RNF40 and its paralog RNF20 form a stable heterodimer complex that can monoubiquitylate histone H2B at lysine 120 as well as other nonhistone proteins. Cancer is a major public he

Molecular BiologyBiochemistry, Genetics and Molecular Biology
12
Article|35 citations·2017
FAS-associated factor-1 positively regulates type I interferon response to RNA virus infection by targeting NLRX1
Jaehoon Kim, Min-Eun Park, Chamilani Nikapitiya, Tae‐Hwan Kim, Md Bashir Uddin, Hyun‐Cheol Lee, Eunhee Kim, Jin Yeul, Jae U. Jung, Chul‐Joong Kim, Jong‐Soo Lee
SJR Q1PLoS PathogensOA

FAS-associated factor-1 (FAF1) is a component of the death-inducing signaling complex involved in Fas-mediated apoptosis. It regulates NF-κB activity, ubiquitination, and proteasomal degradation. Here, we found that FAF1 positively regulates the type I interferon pathway. FAF1gt/gt mice, which deficient in FAF1, and FAF1 knockdown immune cells were highly susceptible to RNA virus infection and showed low levels of inflammatory cytokines and type I interferon (IFN) production. FAF1 was bound comp

ImmunologyImmunology and Microbiology
13
Article|35 citations·2017
Rubicon Modulates Antiviral Type I Interferon (IFN) Signaling by Targeting IFN Regulatory Factor 3 Dimerization
Jaehoon Kim, Tae‐Hwan Kim, Hyun‐Cheol Lee, Chamilani Nikapitiya, Md Bashir Uddin, Min-Eun Park, Prabuddha S. Pathinayake, Eun Seo Lee, Kiramage Chathuranga, Thilina U. B. Herath, W. A. Gayan Chathuranga, Jong‐Soo Lee
SJR Q1Journal of VirologyOA

ABSTRACT Rubicon is part of a Beclin-1-Vps34-containing autophagy complex. Rubicon induces antimicrobial responses upon Toll-like receptor (TLR) stimulation and functions as a feedback inhibitor to prevent unbalanced proinflammatory responses depending on dectin-1 signaling. However, the role played by Rubicon during antiviral immune responses, particularly the type I interferon (IFN) responses, remains largely unknown. Here, we report that Rubicon acts as a negative regulator for virus-triggere

ImmunologyImmunology and Microbiology
14
Article|34 citations·2018
ATP Binding to Rad5 Initiates Replication Fork Reversal by Inducing the Unwinding of the Leading Arm and the Formation of the Holliday Junction
Soochul Shin, Kwangbeom Hyun, Jaehoon Kim, Sungchul Hohng
SJR Q1Cell ReportsOA

Replication fork reversal is one of the major pathways for reactivating stalled DNA replication. Many enzymes with replication fork reversal activity have DNA-unwinding activity as well, but none of the fork reversal enzymes in the SWI/SNF family shows a separate DNA-unwinding activity, raising the question of how they initiate the remodeling process. Here, we found ATP binding to Rad5 induces the unwinding of the leading arm of the replication fork and proximally positions the leading and laggi

Molecular BiologyBiochemistry, Genetics and Molecular Biology
15
Article|31 citations·2011
Nucleosomal H2B ubiquitylation with purified factors
Jaehoon Kim, Robert G. Roeder
SJR Q1MethodsOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology

Research Areas

Molecular BiologyComputer Networks and CommunicationsImmunologyPulmonary and Respiratory MedicineElectrical and Electronic EngineeringHematology

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