Okamoto Kengo

オカモトケンゴ | Okamoto Kengo

Affiliation and department：
Job title： Lecturer
Homepage URL (1)： http://www.takasaki-u.ac.jp/p_yaku/1567/

Research field (2)： Cell biology , Molecular biology

Research keywords (1)： molecular and developmental cell bioloby

Research theme for competitive and other funds (4)：

Papers (13)：

Okamoto K, Tanaka Y, Ogasawara S, Obuse C, Nakayama J, Yano H, Tsuneoka M. KDM2A-dependent reduction of rRNA transcription on glucose starvation requires HP1 in cells, including triple-negative breast cancer cells. Oncotarget. 2019. 10. 46. 4743-4760
Kengo Okamoto, Yuji Tanaka, Makoto Tsuneoka. SF-KDM2A binds to ribosomal RNA gene promoter, reduces H4K20me3 level, and elevates ribosomal RNA transcription in breast cancer cells. INTERNATIONAL JOURNAL OF ONCOLOGY. 2017. 50. 4. 1372-1382
Yuji Tanaka, Hirohisa Yano, Sachiko Ogasawara, Sho-ichi Yoshioka, Hiromi Imamura, Kengo Okamoto, Makoto Tsuneoka. Mild Glucose Starvation Induces KDM2A-Mediated H3K36me2 Demethylation through AMPK To Reduce rRNA Transcription and Cell Proliferation. MOLECULAR AND CELLULAR BIOLOGY. 2015. 35. 24. 4170-4184
Makoto Tsuneoka, Yuji Tanaka, Kengo Okamoto. A CxxC Domain That Binds to Unmethylated CpG Is Required for KDM2A to Control rDNA Transcription. YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN. 2015. 135. 1. 11-21
Yuji Tanaka, Toshiyuki Umata, Kengo Okamoto, Chikashi Obuse, Makoto Tsuneoka. CxxC-ZF Domain Is Needed for KDM2A to Demethylate Histone in rDNA Promoter in Response to Starvation. CELL STRUCTURE AND FUNCTION. 2014. 39. 1. 79-92

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MISC (15)：

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Professional career (1)：

Association Membership(s) (3)：

日本薬学教育学会 , THE JAPANESE BIOCHEMICAL SOCIETY , 日本分子生物学会

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