Updated on 2025/09/30

写真a

 
NAKAMURA NOBUHIRO
 
Organization
School of Life Science and Technology Associate Professor
Title
Associate Professor
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Research Interests

  • 細胞生物学

  • 生化学一般

  • Biochemistry in general

  • 分子生物学

Research Areas

  • Life Science / Molecular biology

  • Life Science / Cell biology

Education

  • Tokyo Institute of Technology   Bioscience and Biotechnology   Biological Sciences

    - 2003

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    Country: Japan

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  • Tokyo Institute of Technology   Graduate School of Bioscience and Biotechnology   Department of Biological Sciences

    - 2003

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  • Tokyo Institute of Technology   School of Bioscience and Biotechnology

    - 1998

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    Country: Japan

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Research History

  • Tokyo Institute of Technology   Associate Professor

    2010.10

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  • 東京工業大学 大学院生命理工学研究科 助手

    2003.4 - 2010.9

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  • 日本学術振興会 特別研究員

    2000.4 - 2003.3

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Professional Memberships

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Papers

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MISC

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Presentations

  • 免疫制御を担う新規受容体分子の肺血管内皮細胞のニコチン応答と炎症応答に及ぼす影響

    中村信大, 山田翔太

    喫煙科学研究財団第37回令和4年度研究助成発表会  2023.7 

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    Event date: 2023.7

    Language:Japanese   Presentation type:Oral presentation (general)  

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  • タバコ煙抽出液処理によるマウス肺血管内皮細胞におけるGタンパク質共役型受容体Adgrf5の発現変動

    山田 翔太, 中村 信大

    第45回日本分子生物学会年会  2022.12 

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    Event date: 2022.12

    Language:Japanese   Presentation type:Poster presentation  

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  • 細胞外マトリックス異常を伴うノックアウトマウスを用いたGPCR分子の新機能解明を目指した研究 Invited

    中村信大, 山田翔太

    第一回LiHubバイオマトリックスミニシンポジウム  2022.11 

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    Event date: 2022.11

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

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  • Targeted disruption of GPR116 (ADGRF5) impairs the integrity of the glomerular filtration barrier in mice Invited

    Nobuhiro Nakamura

    TOIN International Symposium on Biomedical Engineering 2022  2022.11 

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    Event date: 2022.11

    Language:English   Presentation type:Oral presentation (keynote)  

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  • 免疫制御を担う新規受容体分子の肺血管内皮細胞のニコチン応答と炎症応答に及ぼす影響

    中村 信大, 山田 翔太

    喫煙科学研究財団第36回令和3年度研究助成発表会  2022.7 

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    Event date: 2022.7

    Language:Japanese   Presentation type:Oral presentation (general)  

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  • Ubiquitination of syntaxin-6 by the E3 ubiquitin ligase MARCH2

    2020.9 

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    Event date: 2020.9

    Language:Japanese   Presentation type:Poster presentation  

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  • Increased expression of polyamine biosynthetic and catabolic enzymes in alveolar macrophages of Ig-Hepta knockout mice

    Hikaru ANDO, Donna Maretta Ariestanti, Shigehisa HIROSE, Nobuhiro NAKAMURA

    The 9th TOIN International Symposium on Biomedical Engineering 2014  2014.11 

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    Event date: 2014.11

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  • Early cardiac connexin acts as a Ca2+ hemichannel that regulates heart morphogenesis via NFATc4 activation

    Naznin Sultana, Kakon Nag, Akira Kato, Atsushi Kawakami, Koichi Kutsuzawa, Toshihiro Akaike, Shigehisa Hirose, Nobuhiro Nakamura

    The ISSCR 12th Annual Meeting  2014.6 

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    Event date: 2014.6

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  • Regulation of mitochondrial morphology by ubiquitination

    Nobuhiro Nakamura

    International Marine Biotechnology Symposium  2013.5 

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    Event date: 2013.5

    Language:English   Presentation type:Symposium, workshop panel (nominated)  

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  • USP19 deubiquitinating enzyme regulates stability of TEB4 ubiquitin ligase

    Nobuhiro NAKAMURA, Yuki EBISAWA, Shigehisa HIROSE

    Joint Meeting of JSDB 45th and JSCB 64th  2012.5 

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    Event date: 2012.5

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  • Regulation of mitochondrial morphology by ubiquitination Invited

    Nobuhiro Nakamura

    5th Conference of Korean Society for Mitochondrial Research and Medicine  2011.6 

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    Event date: 2011.6

    Language:English   Presentation type:Oral presentation (invited, special)  

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  • ミトコンドリア形態制御因子に相互作用する新規ユビキチン化酵素 MARCH-V の同定 Invited

    中村信大

    第30回日本分子生物学会年会・第80回日本生化学会大会合同大会  2007.12 

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    Event date: 2007.12

    Language:Japanese   Presentation type:Symposium, workshop panel (nominated)  

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  • Cloning and properties of a hypertonicity-inducible inward rectifier K+ channel from euryhaline eels

    Proceedings of the 23rd Taniguchi Foundation Biophysics Symposium  1998 

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    Presentation type:Poster presentation  

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  • Kdg1, a novel RING-finger membrane protein that localizes in the recycling endosome compartment.

    42nd american society for cell biology annual meeting  2002 

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  • Kdg1, a novel RING-finger membrane protein that localizes in the recycling endosome compartment.

    42nd american society for cell biology annual meeting  2002 

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  • Intracellular signaling Mechanism of G-protein coupled receptor ADGRF5

    Tomoya Sato, Masako Kato, Humimasa Kubo, Nobuhiro Nakamura

    13th Toin International Symposium on Biomedical Engineering  2018.10 

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    Language:English   Presentation type:Poster presentation  

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  • Regulatory mechanism of protein expression of human G-protein coupled recept

    2020.9 

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    Language:Japanese   Presentation type:Poster presentation  

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  • Deletion of Adgrf5 causes abnormal glomerular filtration barrier in mice

    2020.9 

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  • A549細胞におけるUSP30-AS1の発現制御とUSP30の発現への影響の解析

    松本 聖慈, 加藤 真子, 中村 信大

    第94回日本生化学大会  2021.11 

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  • The expression of zebrafish cx36.7 gene is regulated by GATA4 in early heart development

    Hisako Miyagi, Ippei Kasajima, Yumiko Tanaka, Keijiro Munakata, Kakon Nag, Naznin Sultana, Shigehisa Hirose, Nobuhiro Nakamura

    2014.5 

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  • Emphysema-like symptoms in lungs of Ig-Hepta/GPR116-deficient mice

    Donna Maretta Ariestanti, Akira Kato, Tomoya Takahashi, Shigehisa Hirose, Nobuhiro Nakamura

    7th international adhesion GPCR workshop  2014.6 

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  • Emphysema-like symptom in Ig-Hepta/Gpr116 knockout mice associated to alveolar macrophage activation

    Donna Maretta Ariestanti, Hikaru Ando, Shigehisa Hirose, Nobuhiro Nobuhiro Nakamura

    10th Toin International Symposium on Biomedical Engineering  2015.11 

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  • Regulation of cardiac-specific expression of the zebrafish cx36.7 gene

    Hisako Miyagi, Kakon Nag, Naznin Sultana, Keijiro Munakata, Shigehisa Hirose, Nobuhiro Nakamura

    Toin International Symposium on Biomedical Engineering  2015.11 

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  • A novel mechanism for the regulation of the expression of the mitochondrial deubiquitinating enzyme USP30

    Mizuho Muto, Masako Kato, Nobuhiro Nakamura

    11th Toin International Symposium on Biomedical Engineering  2016.10 

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  • Adgrf5 deficient mice exhibit bronchial asthma- and fibrosis-like phenotypes

    Fumimasa Kubo, Donna Maretta Ariestanti, Souta Oki, Rahmaningsih Mara Sabirin, Ryotarou Demizu, Nobuhiro Nakamura

    12th Toin International Symposium on Biomedical Engineering  2017.11 

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  • Adgrf5欠損マウスは気管支喘息および肺線維症様の表現型を現す

    久保 文雅, Donna Ariestanti, 沖 颯太, Rahmaningsih Sabirin, 出水 遼太郎, 中村 信大

    2017年度生命科学系学会合同年次大会  2017.12 

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  • Gタンパク質共役型受容体ADGRF5の欠損は肺血管内皮細胞における炎症性分子の発現と喘息に似た表現型を誘導する

    久保 文雅, Donna Ariestanti, 沖 颯太, 福澤拓, 出水 遼太郎, 佐藤朋哉, Rahmaningsih Sabirin, 広瀬茂久, 中村 信大

    第91回日本生化学会大会  2018.9 

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  • Kdg2, a novel multidomain protein involved in the regulation of recycling endosomal trafficking.

    HUPO 2nd & IUBMB XIX World Congress  2003 

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  • Kdg2, a novel multidomain protein involved in the regulation of recycling endosomal trafficking.

    HUPO 2nd & IUBMB XIX World Congress  2003 

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  • Cardiac expression of zebrafish connexin 36.7 is regulated by GATA4 transcription factor

    Hisako Miyagi, Ippei Kasajima, Yumiko Tanaka, Keijiro Munakata, Kakon Nag, Naznin Sultana, Shigehisa Hirose, Nobuhiro Nakamura

    8th International Symposium on Biomedical Engineering  2013.10 

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  • The deubiquitinating enzyme USP19 regulates the ERAD pathway by stabilizing the E3 ubiquitin ligases

    Kumi Harada, Shigehisa Hirose, Nobuhiro Nakamura

    8th International Symposium on Biomedical Engineering  2013.10 

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  • Regulation of the activity of USP19 deubiquitinating enzyme.

    Yuki Ebisawa, Nobuhiro Nakamura

    8th International Symposium on Biomedical Engineering  2013.10 

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  • Control of mitochondrial morphology by ubiquitination and deubiquitination Invited

    Nobuhiro NAKAMURA

    8th International Symposium on Biomedical Engineering  2013.10 

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    Language:English   Presentation type:Oral presentation (keynote)  

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  • Cloning and properties of a hypertonicity-inducible inward rectifier K+ channel from euryhaline eels

    Proceedings of the 23rd Taniguchi Foundation Biophysics Symposium  1998 

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    Presentation type:Poster presentation  

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Research Projects

  • 糸球体の血液濾過フィルターの恒常性維持機構:受容体分子ADGRF5と力学刺激の役割

    Grant number:24K09452  2024.4 - 2027.3

    日本学術振興会  科学研究費助成事業  基盤研究(C)

    中村 信大

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    Grant amount:\4550000 ( Direct Cost: \3500000 、 Indirect Cost:\1050000 )

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  • 新規ホルモンFNDC4とその受容体ADGRF5の血管内皮細胞の機能調節に及ぼす影響に関する研究

    2023.4 - 2024.3

    小柳財団  小柳財団・2023年度研究助成金 

    中村 信大

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    Authorship:Principal investigator 

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  • 免疫制御を担う新規受容体分子の肺血管内皮細胞のニコチン応答と炎症応答に及ぼす影響

    2021.4 - 2024.3

    喫煙科学研究財団  喫煙科学研究財団研究助成(一般研究) 

    中村信大

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  • オーファン受容体Adgrf5による糸球体濾過障壁の恒常性維持機構の解明

    Grant number:21K06167  2021.4 - 2024.3

    日本学術振興会  科学研究費助成事業  基盤研究(C)

    中村 信大

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    Grant amount:\3900000 ( Direct Cost: \3000000 、 Indirect Cost:\900000 )

    ①糸球体血管内皮細胞におけるADGRF5の細胞内シグナル伝達機構について明らかにするため、正常およびADGRF5ノックアウトマウス(以後、KOマウスと呼ぶ)から単離した糸球体および糸球体血管内皮細胞におけるKLF2、KLF4、eNOSの遺伝子発現量について定量PCR解析を行った。その結果、いずれの場合においても遺伝子発現量がKOマウスで上昇することを認めた。タンパク質レベルでもeNOSの発現量増加は確認できたが、eNOSのリン酸化レベルは変化が認められなかった。このことから、KOマウスではKLF2/4を発現誘導するシグナル経路が活性化していることが示唆された。またKOマウスではeNOSのリン酸化レベルが低下し、それを補うためにKLF2/4を介してeNOSの発現を上昇している可能性も考えられる。
    ②KOマウスの糸球体濾過機能異常のメカニズムを解明するために、血管内皮細胞表面に局在しタンパク質透過性を制御する分子の遺伝子発現について解析した。その結果、KOマウスにおけるグリコカリックス成分の遺伝子の発現量が顕著に減少していることを確認した。グリコカリックスの異常はタンパク尿を引き起こすことが報告されていることから、グリコカリックス成分の発現低下がのKOマウスにおけるタンパク尿の発症に寄与する可能性が示唆された。
    ③ADGRF5のリガンドとして新規ホルモン分子であるFNDC4を同定した。FNDC4は肝臓から分泌され、脂肪細胞のADGRF5に作用することでインスリン感受性を上昇させる効果があることを明らかにした。また、脂肪細胞においてFNDC4はADGRF5依存的に細胞内cAMP濃度の上昇を引き起こすことを認めた。

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  • Role of Gpr116 in maintenance of the glomerular filtration barrier in mice

    Grant number:16K07344  2016.4 - 2019.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (C)

    Nakamura Nobuhiro

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    Grant amount:\4680000 ( Direct Cost: \3600000 、 Indirect Cost:\1080000 )

    In this study, 1) we showed that Gpr116 is localized to the glomerular endothelial cells by immunoelectron microscopy. 2) We identified genes of which expression are altered in the glomerular endothelial cells of Gpr116-deficient mice. 3) We identified candidates of downstream signaling molecules, which are activated by Gpr116 overexpression. 4) We observed that several intracellular signaling pathways were activated to a lesser extent in Gpr116 overexpressing cells by shear stress.

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  • ゼブラフィッシュの心筋細胞分化の鍵を担う新規コネキシン分子の機能解析

    2013.4 - 2014.3

    武田科学振興財団  武田科学振興財団ライフサイエンス研究奨励 

    中村信大

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  • Roles of the organelle-specific ubiquitination regulators in protein degradation

    Grant number:24570209  2012.4 - 2015.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (C)

    NAKAMURA Nobuhiro

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    Grant amount:\5070000 ( Direct Cost: \3900000 、 Indirect Cost:\1170000 )

    Although protein quality control is essential for maintaining cellular function, its molecular mechanism is not fully understood. In this study, we performed the characterization of the endoplasmic-reticulum (ER) deubiquitinating enzyme USP19 and showed that USP19 stabilizes the ER-associated ubiquitinating enzyme MARCH6 via deubiquitination. It is known that MARCH6 has a role in protein quality control in the ER. In addition, the stabilization of MARCH6 increases its enzymatic activity and thereby promotes degradation of the mutant ABCB11, a substrate of MARCH6. These results suggest that USP19 is involved in the regulation of protein quality control in the ER.

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  • 細胞内Caシグナルのスイッチとなる新発見のコネキシンの生理機能と発現制御機構

    Grant number:12F02392  2012.4 - 2015.3

    日本学術振興会  科学研究費助成事業  特別研究員奨励費

    中村 信大, SULTANA Naznin, SULTANA N.

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    Grant amount:\2300000 ( Direct Cost: \2300000 )

    私たちは、ゼブラフィッシュおいてコネキシン36.7(Cx36.7)の機能不全が心筋の筋原繊維の配向の乱れを引き起こし、心臓形成と機能不全に至る事を明らかにしてきた。本研究では、コネキシン36.7(Cx36.7)の心筋前駆細胞特異的な発現の調節機構について明らかにする解析を行った。心筋細胞の分化誘導に関与する転写因子の発現パターンについて,心臓形成時のゼブラフィッシュ稚魚を用いてin situ hybridization法により調べ,Cx36.7の発現パターンを比較したところ,発現のタイミングと局在いずれにおいてGata4がCx36.7と一致することが分かった。そこで,Gata4の発現をアンチセンスモルフォリノにより特異的に抑制したところ,Cx36.7遺伝子のプロモーター活性が著しく下がることが分かった。同様な結果は,プロモーター内部のGata型転写因子の結合配列に変異を導入しても認められた。この結合配列がGata4との相互作用部位であることをin vitroのゲルシフト解析で確認した。以上の結果から,Cx36.7遺伝子の心筋細胞特異的な発現はGata4による転写制御によるところが大きいことが分かった。また、Cx36.7の下流のシグナル伝達について解析を行い、候補転写因子を一つ同定することが出きた。現在、この分子の機能解析を行っている。

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  • コネキシンを介したカルシウムシグナリングによる筋原繊維形成の分子機構の解析

    2012.4 - 2013.3

    倉田記念日立科学技術財団  倉田奨励金 

    中村 信大

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  • Cellular role and regulatory mechanism for a novel deubiquitinating enzyme in the endoplasmic reticulum

    Grant number:22770123  2010 - 2011

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Young Scientists (B)

    NAKAMURA Nobuhiro

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    Grant amount:\4030000 ( Direct Cost: \3100000 、 Indirect Cost:\930000 )

    This study has demonstrated that 1) USP19, a transmembrane deubiquitinating enzyme in the endoplasmic reticulum(ER), deubiquitinates not only typical substrates of ER-associated degradation(ERAD), but also ERAD ubiquitinating enzymes, and 2) the enzymatic activity of USP19 is dependent on the domain structures and processing of USP19. These results provide better understand of the molecular mechanism for the regulation of the ERAD pathway as well as the USP19 activity.

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  • Functional characterization of novel proteins involved in mitochondrial dynamics

    Grant number:20770156  2008 - 2009

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Young Scientists (B)

    NAKAMURA Nobuhiro

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    Grant amount:\4030000 ( Direct Cost: \3100000 、 Indirect Cost:\930000 )

    This study has demonstrated that 1) an enzymatic activity of human USP30, a novel mitochondrial deubiquitinating enzyme, is required for maintenance of mitochondrial morphology, and 2) mouse GGNBP1 is highly expressed in spermatogenic cells and induces Drp1-dependent mitochondrial fragmentation. These results provide better understand of the molecular mechanism of mitochondrial dynamics.

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  • 細胞内輸送システムに関与する新しい分子の細胞生物学的研究

    2004 - 2005

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    Grant type:Competitive

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  • Cell biological study for novel molecules involved in intracellular trafficking

    2004 - 2005

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    Grant type:Competitive

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