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関連する概念動画

Positive Regulator Molecules01:45

Positive Regulator Molecules

To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
Positive Regulator Molecules02:39

Positive Regulator Molecules

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.
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

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...
S-Cdk Initiates DNA Replication02:38

S-Cdk Initiates DNA Replication

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 replication.
Inhibition of CDK Activity02:34

Inhibition of CDK Activity

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...
S-Cdk Initiates DNA Replication02:38

S-Cdk Initiates DNA Replication

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 replication.

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関連する実験動画

Updated: Jun 21, 2026

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

サイクリンE-CDK2なしの細胞増殖

Juan Méndez1

  • 1Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.

Cell
|August 28, 2003
PubMed
まとめ

マウスはサイクリンE1とE2なしで発達できるが,これらのタンパク質は細胞サイクル進行に不可欠である. 具体的には,サイクリンE1とE2は,マウス細胞のエンドレプリケーションと退出静止に不可欠です.

科学分野:

  • 細胞生物学 細胞生物学
  • 発達生物学 発達生物学とは
  • 分子遺伝学 分子遺伝学

背景:

  • サイクリンは,細胞循環の重要な調節因子である.
  • サイクリンEタンパク質 (E1およびE2) は,細胞増殖に役割を果たすことが知られている.
  • 哺乳類の胚発達と細胞サイクル終了におけるサイクリンE1とE2の特定の必要性は,完全に解明されていません.

研究 の 目的:

  • マウスの胚発達におけるサイクリンE1とE2の役割を調査する.
  • 繊維細胞増殖におけるサイクリンE1とE2の機能を決定する.
  • サイクリンE1とE2のエンドレプリケーションおよび静止状態からの脱出の必要性を評価する.

主な方法:

  • サイクリンE1とサイクリンE2の両方の遺伝子が欠けているマウスの世代 (ダブルノックアウト).
  • ダブル・ノックアウト胚から得られた線維芽細胞の培養と分析.
  • 野生型およびノックアウト型細胞における細胞増殖,エンドレプリケーション,静止状態からの脱出の評価.

主要な成果:

  • サイクリンE1とE2が欠けているマウスは,胚の発達を完了することができます.
  • ダブル・ノックアウト胚の線維芽細胞は,in vitroでは正常な増殖を示しています.

さらに関連する動画

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

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
12:26

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

Published on: May 3, 2018

関連する実験動画

Last Updated: Jun 21, 2026

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

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

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
12:26

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

Published on: May 3, 2018

  • サイクリンE1とE2は,エンドレプリケーションと静止状態から活性細胞サイクルへの移行に不可欠です.

    • 結論:

    • サイクリンE1とE2は,胚の発達や基礎線維芽細胞の増殖に不可欠ではありません.
    • これらの特定のサイクリンは,細胞周期の特殊なプロセス,すなわちエンドレプリケーションと静止状態からの脱出において重要な役割を果たします.