Jove
Visualize
联系我们

相关概念视频

Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.8K
DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
5.8K
The DNA Replication Fork01:02

The DNA Replication Fork

36.1K
An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication...
36.1K
DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

9.2K
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...
9.2K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

10.0K
Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
10.0K
Replication in Eukaryotes01:29

Replication in Eukaryotes

14.0K
In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
14.0K
Negative Regulator Molecules01:23

Negative Regulator Molecules

35.5K
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.
35.5K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same journal

Brain Network Connectivity Predicts Survival in Diffuse Midline Glioma.

Cancer discovery·2026
Same journal

First-in-human testing of a mutant KRAS vaccine for pancreatic cancer interception in high-risk cohorts.

Cancer discovery·2026
Same journal

CDK8 Inhibition Releases the Muscle Differentiation Block in Fusion-driven Alveolar Rhabdomyosarcoma.

Cancer discovery·2026
Same journal

CDK8 inhibition induces Mediator trapping and impairment of the EWSR1::FLI1 transcriptional program in Ewing sarcoma.

Cancer discovery·2026
Same journal

SEZ6-Targeted ADC Shows Preliminary Efficacy in Small Cell Lung Cancer.

Cancer discovery·2026
Same journal

Nonprofit Acquires Abandoned Leukemia Drug Supply.

Cancer discovery·2026
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关实验视频

Updated: Jul 21, 2025

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

27.4K

药物阻止复制比想象中的更晚.

    Cancer discovery
    |July 25, 2023
    PubMed
    概括

    循环素依赖性激酶4/6 (CDK4/6) 抑制剂通过阻止细胞复制,在乳腺癌治疗中表现有前途. 需要进一步的研究来确认不可逆转的细胞衰老,并防止疾病复发.

    科学领域:

    • 在瘤学瘤学.
    • 细胞生物学 细胞生物学

    背景情况:

    • 包括palbociclib在内的循环素依赖性激酶4/6 (CDK4/6) 抑制剂正在成为乳腺癌的有前途的治疗策略.
    • 新出现的数据表明,这些抑制剂可以在细胞周期的后期阶段逆转细胞复制,比以前理解的,这表明扩大临床益处的潜力.

    研究的目的:

    • 研究CDK4/6抑制剂在结合化疗时诱导不可逆细胞衰老的疗效.
    • 为了解决进一步研究的需要,以确认CDK4/6抑制剂加上化疗方案的长期益处和安全性.

    主要方法:

    • 这项研究的重点是分析现有数据和关于CDK4/6抑制剂在乳腺癌治疗中的机制的持续研究.
    • 评估治疗细胞中细胞复制的潜力和疾病复发的风险.

    主要成果:

    • 初步数据表明,CDK4/6抑制剂可以在细胞循环的先进阶段停止细胞复制,这可能导致更好的治疗结果.
    • 仍然存在对治疗细胞的稳定性和由于不完全衰老而导致疾病复发的风险的担忧.

    结论:

    • CDK4/6抑制剂代表了乳腺癌治疗的重大进展,具有更广泛的临床应用的潜力.
    • 进一步的研究至关重要,以验证不可逆转的细胞衰老的诱导,并减轻使用CDK4/6抑制剂和化疗治疗的患者瘤复发的风险.

    更多相关视频

    Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
    07:27

    Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase

    Published on: April 29, 2010

    13.7K
    Author Spotlight: Investigating the Motion Dynamics of the Eukaryotic Replisome Components at the Single-Molecule Level
    10:11

    Author Spotlight: Investigating the Motion Dynamics of the Eukaryotic Replisome Components at the Single-Molecule Level

    Published on: July 26, 2024

    1.1K

    相关实验视频

    Last Updated: Jul 21, 2025

    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

    27.4K
    Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
    07:27

    Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase

    Published on: April 29, 2010

    13.7K
    Author Spotlight: Investigating the Motion Dynamics of the Eukaryotic Replisome Components at the Single-Molecule Level
    10:11

    Author Spotlight: Investigating the Motion Dynamics of the Eukaryotic Replisome Components at the Single-Molecule Level

    Published on: July 26, 2024

    1.1K