Complex formation of sphingomyelin synthase with glucosylceramide synthase increases sphingomyelin and decreases glucosylceramide levels
| Project/Area Number |
18K06635
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Review Section |
Basic Section 47030:Pharmaceutical hygiene and biochemistry-related
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| Research Institution | Teikyo University |
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Principal Investigator |
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| Project Period (FY) |
2018-04-01 – 2021-03-31
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| Project Status |
Completed (Fiscal Year 2020)
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| Budget Amount *help |
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2020: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2019: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2018: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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| Keywords | 脂質代謝酵素 / スフィンゴミエリン合成酵素 / ヘテロ複合体 / オリゴマー |
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| Outline of Final Research Achievements |
Sphingomyelin synthase 1 (SMS1) and glucosylceramide synthase (GlcT) are key enzymes that catalyze the conversion of ceramide (Cer) to sphingomyelin (SM) and glucosylceramide (GlcCer), respectively. GlcCer synthesis has been postulated to occur mainly in cis-Golgi, and SM synthesis is thought to occur in medial/trans-Golgi; however, SMS1 and GlcT are known to partially colocalize in cisternae, especially in medial/trans-Golgi. Here, we report that SMS1 and GlcT can form a heteromeric complex, in which the N terminus of SMS1 and the C terminus of GlcT are in close proximity. Deletion of the N-terminal sterile alpha motif of SMS1 reduced the stability of the SMS1/GlcT complex, resulting in a significant reduction in SM synthesis in vivo. In contrast, chemical-induced heterodimerization augmented SMS1 activity, depending on an increase in the amount and stability of the complex. These results suggest that formation of the SMS1/GlcT heteromeric complex increases SM synthesis.
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| Academic Significance and Societal Importance of the Research Achievements |
近年、SMはメタボリックシンドロームへの関与のみならず、機能性食品素材としても注目されている。このことは、SM量は生体内で適切にコントロールされるべきであり、体内でのSM量の過剰な産生および減少は、私たちの健康寿命を縮めることを示唆している。本研究は、SM産生の制御のメカニズムの一部を解明したという学術的な発見にとどまらず、SMのメタボリックシンドロームへの関与を解明する研究基盤へと繋がっていくことが期待される。
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Report
(4 results)
Research Products
(11 results)
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[Journal Article] Complex formation of sphingomyelin synthase 1 with glucosylceramide synthase increases sphingomyelin and decreases glucosylceramide levels2018
Author(s)
Yasuhiro Hayashi , Yoko Nemoto-Sasaki, Naoki Matsumoto, Kotaro Hama, Takashi Tanikawa, Saori Oka, Tadaaki Saeki, Tatsuya Kumasaka, Takanori Koizumi, Seisuke Arai, Ikuo Wada, Kazuaki Yokoyama, Takayuki Sugiura, and Atsushi Yamashita
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Journal Title
Journal of Biological Chemistry
Volume: 293
Issue: 45
Pages: 17505-17522
DOI
Related Report
Peer Reviewed
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