Woojin An
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View article: Functional unfolding of the integrin αX transmembrane helix
Functional unfolding of the integrin αX transmembrane helix Open
In biological membranes, proteins face a fundamentally different environment than in water. To avoid untenable lipid contacts with polar backbone atoms, they use the continuous hydrogen bonding achieved by α-helices or β-barrels to travers…
View article: Exploring the Sustainability of Sports OTT Service
Exploring the Sustainability of Sports OTT Service Open
In South Korea, Generation Z’s influence on the growth of sports over-the-top (OTT) services is significant. For sustainable growth, OTT service providers need to focus on converting existing users into loyal customers. In this context, un…
View article: VprBP regulates osteoclast differentiation via an epigenetic mechanism involving histone H2A phosphorylation
VprBP regulates osteoclast differentiation via an epigenetic mechanism involving histone H2A phosphorylation Open
View article: Promoter hypermethylation as a novel regulator of ANO1 expression and function in prostate cancer bone metastasis
Promoter hypermethylation as a novel regulator of ANO1 expression and function in prostate cancer bone metastasis Open
View article: <scp>MMP</scp>‐9‐dependent proteolysis of the histone <scp>H3</scp> N‐terminal tail: a critical epigenetic step in driving oncogenic transcription and colon tumorigenesis
<span>MMP</span>‐9‐dependent proteolysis of the histone <span>H3</span> N‐terminal tail: a critical epigenetic step in driving oncogenic transcription and colon tumorigenesis Open
Matrix metalloproteinase 9 (MMP‐9) is a member of the MMP family and has been recently identified as a nuclear protease capable of clipping histone H3 N‐terminal tails (H3NT). This MMP‐9 ‐dependent H3NT proteolysis is critical for establis…
View article: Non-canonical MLL1 activity regulates centromeric phase separation and genome stability
Non-canonical MLL1 activity regulates centromeric phase separation and genome stability Open
View article: VprBP/DCAF1 Triggers Melanomagenic Gene Silencing through Histone H2A Phosphorylation
VprBP/DCAF1 Triggers Melanomagenic Gene Silencing through Histone H2A Phosphorylation Open
Vpr binding protein (VprBP), also known as DDB1- and CUL4-associated factor1 (DCAF1), is a recently identified atypical kinase and plays an important role in downregulating the transcription of tumor suppressor genes as well as increasing …
View article: VprBP/DCAF1 triggers melanomagenic gene silencing through histone H2A phosphorylation
VprBP/DCAF1 triggers melanomagenic gene silencing through histone H2A phosphorylation Open
Background Melanoma is the most aggressive form of skin cancer arising from pigment-producing melanocytes and is often associated with dysregulation of epigenetic factors targeting histones. VprBP, also known as DCAF1, is a recently identi…
View article: VprBP/DCAF1 triggers melanomagenic gene silencing through histone H2A phosphorylation
VprBP/DCAF1 triggers melanomagenic gene silencing through histone H2A phosphorylation Open
Background Melanoma is the most aggressive form of skin cancer arising from pigment-producing melanocytes and is often associated with dysregulation of epigenetic factors targeting histones. VprBP, also known as DCAF1, is a recently identi…
View article: DCAF1/VprBP triggers melanomagenic gene silencing through histone H2A phosphorylation
DCAF1/VprBP triggers melanomagenic gene silencing through histone H2A phosphorylation Open
View article: Phosphorylation and stabilization of EZH2 by DCAF1/VprBP trigger aberrant gene silencing in colon cancer
Phosphorylation and stabilization of EZH2 by DCAF1/VprBP trigger aberrant gene silencing in colon cancer Open
Our recent work has shown that DCAF1 (also known as VprBP) is overexpressed in colon cancer and phosphorylates histone H2AT120 to drive epigenetic gene inactivation and oncogenic transformation. We have extended these observations by inves…
View article: VprBP/DCAF1 regulates p53 function and stability through site-specific phosphorylation
VprBP/DCAF1 regulates p53 function and stability through site-specific phosphorylation Open
VprBP (also known as DCAF1) is a recently identified kinase that is overexpressed in cancer cells and serves as a major determinant for epigenetic gene silencing and tumorigenesis. The role of VprBP in driving target gene inactivation has …
View article: DNMT and EZH2 inhibitors synergize to activate therapeutic targets in hepatocellular carcinoma
DNMT and EZH2 inhibitors synergize to activate therapeutic targets in hepatocellular carcinoma Open
View article: mAM Facilitates Conversion by ESET of Dimethyl to Trimethyl Lysine 9 of Histone H3 to Cause Transcriptional Repression
mAM Facilitates Conversion by ESET of Dimethyl to Trimethyl Lysine 9 of Histone H3 to Cause Transcriptional Repression Open
Methylation of histone tails plays an important role in chromatin structure and function. Previously, we reported that ESET/SETDB1 is a histone methyltransferase (HMTase). Here, we show that SETDB1 tightly associates with the human homolog…
View article: VprBP directs epigenetic gene silencing through histone H2A phosphorylation in colon cancer
VprBP directs epigenetic gene silencing through histone H2A phosphorylation in colon cancer Open
Histone modification is aberrantly regulated in cancer and generates an unbalanced state of gene transcription. VprBP, a recently identified kinase, phosphorylates histone H2A on threonine 120 (T120) and is involved in oncogenic transcript…
View article: Author response for "VprBP directs epigenetic gene silencing through histone H2A phosphorylation in colon cancer"
Author response for "VprBP directs epigenetic gene silencing through histone H2A phosphorylation in colon cancer" Open
View article: Author response for "VprBP directs epigenetic gene silencing through histone H2A phosphorylation in colon cancer"
Author response for "VprBP directs epigenetic gene silencing through histone H2A phosphorylation in colon cancer" Open
View article: MMP-2 is a novel histone H3 N-terminal protease necessary for myogenic gene activation
MMP-2 is a novel histone H3 N-terminal protease necessary for myogenic gene activation Open
View article: Insight Into Pathological Integrin αIIbβ3 Activation From Safeguarding The Inactive State
Insight Into Pathological Integrin αIIbβ3 Activation From Safeguarding The Inactive State Open
View article: Linker Histone H1.2 Cooperates with Cul4A and PAF1 to Drive H4K31 Ubiquitylation-Mediated Transactivation
Linker Histone H1.2 Cooperates with Cul4A and PAF1 to Drive H4K31 Ubiquitylation-Mediated Transactivation Open
Increasing evidence suggests that linker histone H1 can influence distinct cellular processes by acting as a gene-specific regulator. However, the mechanistic basis underlying such H1 specificity and whether H1 acts in concert with other c…
View article: A <i>HOTAIR</i> regulatory element modulates glioma cell sensitivity to temozolomide through long-range regulation of multiple target genes
A <i>HOTAIR</i> regulatory element modulates glioma cell sensitivity to temozolomide through long-range regulation of multiple target genes Open
Temozolomide (TMZ) is a frequently used chemotherapy for glioma; however, chemoresistance is a major problem limiting its effectiveness. Thus, knowledge of mechanisms underlying this outcome could improve patient prognosis. Here, we report…
View article: Epigenetic Modification as a Regulatory Mechanism for Spatiotemporal Dynamics of ANO1 Expression in Salivary Glands
Epigenetic Modification as a Regulatory Mechanism for Spatiotemporal Dynamics of ANO1 Expression in Salivary Glands Open
Anoctamin1 (ANO1), a calcium activated chloride channel, is known to play a critical role in salivary secretion. In the salivary gland, ANO1 is expressed exclusively in the acinar cells, with no expression in the ductal cells. However, the…
View article: p32 is a negative regulator of p53 tetramerization and transactivation
p32 is a negative regulator of p53 tetramerization and transactivation Open
p53 is a sequence‐specific transcription factor, and proper regulation of p53 transcriptional activity is critical for orchestrating different tumor‐suppressive mechanisms. p32 is a multifunctional protein which interacts with a large numb…
View article: DNMT and HDAC inhibitors modulate MMP-9-dependent H3 N-terminal tail proteolysis and osteoclastogenesis
DNMT and HDAC inhibitors modulate MMP-9-dependent H3 N-terminal tail proteolysis and osteoclastogenesis Open
View article: Regulation of Breast Cancer-Induced Osteoclastogenesis by MacroH2A1.2 Involving EZH2-Mediated H3K27me3
Regulation of Breast Cancer-Induced Osteoclastogenesis by MacroH2A1.2 Involving EZH2-Mediated H3K27me3 Open
View article: MacroH2A1.2 inhibits prostate cancer-induced osteoclastogenesis through cooperation with HP1α and H1.2
MacroH2A1.2 inhibits prostate cancer-induced osteoclastogenesis through cooperation with HP1α and H1.2 Open
View article: H3K27me1 is essential for MMP-9-dependent H3N-terminal tail proteolysis during osteoclastogenesis
H3K27me1 is essential for MMP-9-dependent H3N-terminal tail proteolysis during osteoclastogenesis Open
View article: Membrane Anchoring of α-Helical Proteins: Role of Tryptophan
Membrane Anchoring of α-Helical Proteins: Role of Tryptophan Open
The function of membrane proteins relies on a defined orientation of protein relative to lipid. In apparent correlation to protein anchoring, tryptophan residues are enriched in the lipid headgroup region. To characterize the thermodynamic…
View article: Role of remodeling and spacing factor 1 in histone H2A ubiquitination-mediated gene silencing
Role of remodeling and spacing factor 1 in histone H2A ubiquitination-mediated gene silencing Open
Significance Histone H2AK119 ubiquitination (H2Aub), as mediated by Polycomb repressive complex 1 (PRC1), is a prevalent modification which has been linked to gene silencing. We report that remodeling and spacing factor 1 (RSF1), a subunit…
View article: Correction for Kim et al., “Vpr-Binding Protein Antagonizes p53-Mediated Transcription via Direct Interaction with H3 Tail”
Correction for Kim et al., “Vpr-Binding Protein Antagonizes p53-Mediated Transcription via Direct Interaction with H3 Tail” Open