Jove
Visualize
联系我们
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

相关概念视频

PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

5.4K
The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
5.4K
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

5.5K
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...
5.5K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

4.6K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
4.6K
MAPK Signaling Cascades01:07

MAPK Signaling Cascades

7.9K
Mitogen-activated protein kinase, or MAPK pathway, activates three sequential kinases to regulate cellular responses such as proliferation, differentiation, survival, and apoptosis. The canonical MAPK pathway starts with a mitogen or growth factor binding to an RTK. The activated RTKs stimulate Ras, which recruits Raf or MAP3 Kinase (MAPKKK), the first kinase of the MAPK signaling cascade. Raf further phosphorylates and activates MEK or MAP2 Kinases (MAPKK), which in turn phosphorylates MAP...
7.9K
The JAK-STAT Signaling Pathway01:20

The JAK-STAT Signaling Pathway

12.1K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as  SH2...
12.1K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

6.3K
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,...
6.3K

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 author

A diagnostic performance study of multiplex polymerase chain reaction-based targeted next-generation sequencing for the accurate identification of <i>Mycobacterium</i> tuberculosis in bronchoalveolar lavage fluid.

Frontiers in cellular and infection microbiology·2026
Same author

Predictors of intermaxillary fixation (IMF) after open reduction and internal fixation (ORIF) in maxillofacial fractures: A retrospective cohort study.

National journal of maxillofacial surgery·2026
Same author

From Diagnostic Concordance to Implementation-grade Lung Ultrasound in Critical Care.

Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine·2026
Same author

An Expanded T2-FLAIR Mismatch Phenotype in IDH-Mutant Astrocytomas.

Journal of magnetic resonance imaging : JMRI·2026
Same author

Desflurane combined with ciprofol or esketamine improves postoperative symptoms without compromising early neurocognitive recovery after intracranial aneurysm endovascular coiling.

Frontiers in medicine·2026
Same author

A novel composite model of PTSD induced by social bullying: validation via multidimensional behavioral and molecular biomarkers.

Molecular psychiatry·2026

相关实验视频

Updated: Jan 17, 2026

Real-Time Monitoring of Aurora kinase A Activation using Conformational FRET Biosensors in Live Cells
06:29

Real-Time Monitoring of Aurora kinase A Activation using Conformational FRET Biosensors in Live Cells

Published on: July 30, 2020

3.4K

BRD4 调节了 Aurora B 激酶活性.

Ballachanda N Devaiah1, Dan Cheng1, Amit K Singh1

  • 1Experimental Immunology Branch, NCI, NIH, Bethesda, MD 20892, USA.

bioRxiv : the preprint server for biology
|September 19, 2025
PubMed
概括

odomain 4 (BRD4) 通过抑制 Aurora B 激酶活性来控制线粒分裂. 基激活酸化BRD4,使其从染色质中释放出来,使Aurora B在转化阶段发挥作用.

科学领域:

  • 分子生物学分子生物学
  • 细胞生物学 细胞生物学
  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.

背景情况:

  • odomain 4 (BRD4) 是染色质结构和转录的关键调节者.
  • BRD4在癌症和免疫反应中起着重要作用.
  • 与其他转录调节剂不同的是,BRD4在早期线粒分裂期间仍然与染色质结合.

研究的目的:

  • 为了研究BRD4在调节线粒分裂中的作用.
  • 为了阐明BRD4和Aurora B激酶之间的相互作用.
  • 了解BRD4的线粒功能是如何调节的.

主要方法:

  • 研究了BRD4和Aurora B激酶之间的直接相互作用.
  • 评估了BRD4结合对奥罗拉B激酶活性的影响.
  • 检查了基因素H3和MCAK的酸化.
  • 分析了JNK激活在BRD4从染色质释放中的作用.

主要成果:

  • BRD4 直接与 Aurora B 激酶活性结合并抑制它.
  • 结合BRD4可以防止Aurora B的自酸化,以及组织蛋白H3和MCAK的酸化.
关键词:
极光 B 极光 B 极光这是一种BRD4激酶.在JNK中,JNK就是JNK.线粒分裂 (mitosis) 是一种发生在细胞的过程.甲基基因素的基因素是甲基基因素的基因.

更多相关视频

Author Spotlight: Integrating BRET-Based Assays and Rare Mutation Analysis to Decipher RAF Kinase Regulation in Live Cells
06:44

Author Spotlight: Integrating BRET-Based Assays and Rare Mutation Analysis to Decipher RAF Kinase Regulation in Live Cells

Published on: March 1, 2024

1.7K
Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
07:49

Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods

Published on: July 17, 2019

6.5K

相关实验视频

Last Updated: Jan 17, 2026

Real-Time Monitoring of Aurora kinase A Activation using Conformational FRET Biosensors in Live Cells
06:29

Real-Time Monitoring of Aurora kinase A Activation using Conformational FRET Biosensors in Live Cells

Published on: July 30, 2020

3.4K
Author Spotlight: Integrating BRET-Based Assays and Rare Mutation Analysis to Decipher RAF Kinase Regulation in Live Cells
06:44

Author Spotlight: Integrating BRET-Based Assays and Rare Mutation Analysis to Decipher RAF Kinase Regulation in Live Cells

Published on: March 1, 2024

1.7K
Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
07:49

Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods

Published on: July 17, 2019

6.5K
  • 转基因激活酸化BRD4,导致其在转基因阶段从染色质中暂时释放.
  • 极光B活性与BRD4结合相反相关,与JNK激活直接相关.
  • 结论:

    • BRD4在线粒分裂过程中直接控制Aurora B激酶活性.
    • 通过JNK介导的BRD4酸化是将其从染色质释放的关键步骤,允许Aurora B激活.
    • 这揭示了涉及BRD4,Aurora B和JNK的线粒分裂的新型调节机制.