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S-Cdk Initiates DNA Replication02:38

S-Cdk Initiates DNA Replication

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The cell cycle is a series of events leading to DNA duplication followed by the division of cell content to form two daughter cells. The cell cycle progresses in four stages—the cell increases in size (gap 1 or G1-phase), duplicates its DNA (synthesis or S-phase), prepares to divide (gap 2 or G2-phase), and divides (mitosis or M-phase).
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of...
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Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

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The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
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DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

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In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
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Negative Regulator Molecules01:23

Negative Regulator Molecules

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Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
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Positive Regulator Molecules02:39

Positive Regulator Molecules

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Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
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The Cell Cycle Control System01:28

The Cell Cycle Control System

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The cell cycle regulation directs how a cell proceeds from one phase to the next and begins mitosis. The cell cycle control system includes intracellular regulatory molecules and external triggers. They provide "stop" or "advance" signals and operate at specific cell cycle stages termed checkpoints to ensure that a particular process is completed before the cell advances to the next phase.
Cyclins and cyclin-dependent kinases (Cdks) are the primary cell cycle regulators and...
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  2. G2停止中に Cdk4/6の活性が要求され,ストレス誘発性エンドレプリケーションを防止する.
  1. ホーム
  2. G2停止中に Cdk4/6の活性が要求され,ストレス誘発性エンドレプリケーションを防止する.

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Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
12:02

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols

Published on: June 6, 2017

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G2停止中に CDK4/6の活性が要求され,ストレス誘発性エンドレプリケーションを防止する.

Connor McKenney1,2,3, Yovel Lendner1,2, Adler Guerrero Zuniga1,2,3

  • 1Department of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Science (New York, N.Y.)
|May 2, 2024

PubMed で要約を見る

まとめ
この要約は機械生成です。

細胞分裂には,サイクリン依存キナーゼ (CDK) による細胞周期調節が不可欠である. この研究は,CDK4/6がG2状態を維持し,細胞周期の不可逆性を挑戦し,ストレス後の全ゲノム倍増を示しています.

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Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis
08:33

Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis

Published on: December 5, 2017

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Author Spotlight: Visualizing Single-Stranded DNA During DNA Repair for Therapeutic Insights
08:30

Author Spotlight: Visualizing Single-Stranded DNA During DNA Repair for Therapeutic Insights

Published on: December 22, 2023

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関連する実験動画

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
12:02

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols

Published on: June 6, 2017

27.3K
Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis
08:33

Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis

Published on: December 5, 2017

14.3K
Author Spotlight: Visualizing Single-Stranded DNA During DNA Repair for Therapeutic Insights
08:30

Author Spotlight: Visualizing Single-Stranded DNA During DNA Repair for Therapeutic Insights

Published on: December 22, 2023

2.4K

科学分野:

  • 細胞生物学
  • 分子生物学
  • 遺伝学

背景:

  • 細胞周期の進行は,サイクリン依存キナーゼ (CDKs) によって緊密に制御されます.
  • CDK4/ 6とCDK2は,ミトゲンシグナルに反応して,G1からS相への移行を制御する.
  • 確立された見解は,細胞サイクル不可逆性の制限後のポイントを仮定します.

研究 の 目的:

  • G2受容細胞における細胞周期調節体の役割を調査する.
  • 細胞サイクルの不可逆性の概念と 制限点以降のミトゲンへの要求に異議を唱える
  • G2 脱出とそれ以降のゲノムイベントの背後にあるメカニズムを解明する.

主な方法:

  • G2受容細胞における細胞周期調節の分析
  • G2状態の維持におけるCDK4/6とCDK2の役割を調査する.
  • ストレス誘発のG2脱出を ストレス誘発のタンパク質キナーゼによって 媒介する

主要な成果:

  • CDK4/ 6媒介メカニズムは,通常G1で活性化され,G2受容細胞では細胞サイクル終了を防ぐために必要である.
  • CDK4/6は,細胞周期の可塑性を示すG2状態を維持する役割を果たします.
  • リボトキシカル・ストレスは,ストレスを誘発したタンパク質キナーゼを通じたG2の脱出を誘発し,ストレスの軽減時に全ゲノムの倍増につながります.
  • 結論:

    • 細胞循環は完全に不可逆的ではなく,制限点を超えてミトゲンが必要になる可能性があります.
    • CDK4/6はG2停止を維持する新しい機能を持っています.
    • ストレスによる細胞サイクル終了は,全ゲノム倍増につながり,細胞プロイディに影響を及ぼします.