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Your search keyword '"Kang, Joo-Young"' showing total 27 results
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27 results on '"Kang, Joo-Young"'

21. KDM2B is a histone H3K79 demethylase and induces transcriptional repressionviasirtuin‐1‐mediated chromatin silencing

Author

Kang, Joo‐Young, primary, Kim, Ji‐Young, additional, Kim, Kee‐Beom, additional, Park, Jin Woo, additional, Cho, Hana, additional, Hahm, Ja Young, additional, Chae, Yun‐Cheol, additional, Kim, Daehwan, additional, Kook, Hyun, additional, Rhee, Sangmyeong, additional, Ha, Nam‐Chul, additional, and Seo, Sang‐Beom, additional

Published
2018
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26. Inhibition of FoxO1 acetylation by INHAT subunit SET/TAF‐Iβ induces p21 transcription.

Author

Chae, Yun-Cheol, Kim, Kee-Beom, Kang, Joo-Young, Kim, Se-Ryeon, Jung, Hyeon-Soo, and Seo, Sang-Beom

Abstract

Post‐translational modification of forkhead family transcription factor, FoxO1, is an important regulatory mode for its diverse activities. FoxO1 is acetylated by HAT coactivators and its transcriptional activity is decreased via reduced DNA binding affinity. Here, we report that SET/TAF‐Iβ inhibited p300‐mediated FoxO1 acetylation in an INHAT domain‐dependent manner. SET/TAF‐Iβ interacted with FoxO1 and activated transcription of FoxO1 target gene, p21. Moreover, SET/TAF‐Iβ inhibited acetylation of FoxO1 and increased p21 transcription induced by oxidative stress. Our results suggest that SET/TAF‐Iβ inhibits FoxO1 acetylation and activates its transcriptional activity toward p21.SET/TAF‐Iβ inhibits FoxO1 acetylation. SET/TAF‐Iβ interacts with FoxO1 in INHAT domain dependent manner. Recruitment of FoxO1 on p21 promoter is increased by SET/TAF‐Iβ. SET/TAF‐Iβ induces p21 transcription and apoptosis under oxidative stress. [ABSTRACT FROM AUTHOR]

Published
2014
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27. KDM2B is a histone H3K79 demethylase and induces transcriptional repression via sirtuin-1-mediated chromatin silencing.

Author

Kang JY, Kim JY, Kim KB, Park JW, Cho H, Hahm JY, Chae YC, Kim D, Kook H, Rhee S, Ha NC, and Seo SB

Subjects
Chromatin genetics, F-Box Proteins genetics, Homeodomain Proteins genetics, Humans, Jumonji Domain-Containing Histone Demethylases genetics, K562 Cells, Myeloid Ecotropic Viral Integration Site 1 Protein genetics, Sirtuin 1 genetics, Chromatin metabolism, F-Box Proteins metabolism, Gene Silencing, Homeodomain Proteins biosynthesis, Jumonji Domain-Containing Histone Demethylases metabolism, Myeloid Ecotropic Viral Integration Site 1 Protein biosynthesis, Sirtuin 1 metabolism, Transcription, Genetic
Abstract

The methylation of histone H3 lysine 79 (H3K79) is an active chromatin marker and is prominent in actively transcribed regions of the genome; however, demethylase of H3K79 remains unknown despite intensive research. Here, we show that KDM2B, also known as FBXL10 and a member of the Jumonji C family of proteins known for its histone H3K36 demethylase activity, is a di- and trimethyl H3K79 demethylase. We demonstrate that KDM2B induces transcriptional repression of HOXA7 and MEIS1 via occupancy of promoters and demethylation of H3K79. Furthermore, genome-wide analysis suggests that H3K79 methylation levels increase when KDM2B is depleted, which indicates that KDM2B functions as an H3K79 demethylase in vivo. Finally, stable KDM2B-knockdown cell lines exhibit displacement of NAD + -dependent deacetylase sirtuin-1 (SIRT1) from chromatin, with concomitant increases in H3K79 methylation and H4K16 acetylation. Our findings identify KDM2B as an H3K79 demethylase and link its function to transcriptional repression via SIRT1-mediated chromatin silencing.-Kang, J.-Y., Kim, J.-Y., Kim, K.-B., Park, J. W., Cho, H., Hahm, J. Y., Chae, Y.-C., Kim, D., Kook, H., Rhee, S., Ha, N.-C., Seo, S.-B. KDM2B is a histone H3K79 demethylase and induces transcriptional repression via sirtuin-1-mediated chromatin silencing.

Published
2018
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