Cdc2キナーゼは,cis-Golgiマトリックスタンパク質GM130を直接リン酸化し,ミトーシスのGolgi断片化に必要とされる
M Lowe1, C Rabouille, N Nakamura
1Cell Biology Laboratory, Imperial Cancer Research Fund, London, United Kingdom.
Cell
|September 30, 1998
まとめ
ミトティック・ゴルギの断片化は,Cdc2キナーゼにより,Ser-25でGM130をリン酸化し,p115結合を阻害する. このプロセスはMEK1 MAPキナーゼ経路を必要としません.
科学分野:
- 細胞生物学 細胞生物学
- 分子生物学は分子生物学である.
- バイオケミストリー バイオケミストリー
背景:
- ミトス・ゴルギ分裂は,細胞分裂中の重要な出来事です.
- GM130とp115の相互作用の破壊は,ゴルギの断片化を誘導すると考えられている.
- 関連する正確な分子機構とシグナル伝達経路は,まだ完全に理解されていません.
研究 の 目的:
- ミトーシス中のGM130の破壊に責任を負う特定のキナーゼとリン酸化部位を特定する.
- ミトスのゴルギ分裂におけるMEK1-MAPキナーゼ経路の役割を調査する.
主な方法:
- 責任のあるキナーゼを特定するためのインビトロキナーゼアッセイ.
- サイト・ディレクテッド・ミュータゲネシスにより,GM130.0の重要なリン酸化部位を特定する.
- MEKの必要性を評価するためのインビトロおよびインビボ実験1.
主要な成果:
- GM130のセリン-25 (Ser-25) は,重要なリン酸化部位として特定されました.
- Cdc2キナーゼは,Ser-25.5でのGM130のリン酸化に責任を負う酵素として特定されました.
- MEK1はGM130のリン酸化やゴルギ分裂には必要ではないことが判明しました.
結論:
- Cdc2は,GM130をセル25で直接リン酸化し,ゴルギ分裂を引き起こします.
- MEK1-MAPキナーゼ経路は,ミトスのゴルギ分裂に不可欠ではありません.
- この研究は,基本的な細胞分裂プロセスにおけるキナーゼの直接的関与を明らかにしています.
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