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

Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

7.2K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
7.2K
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

7.5K
Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
7.5K
Abnormal Proliferation02:23

Abnormal Proliferation

4.6K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.6K
Chromatin Position Affects Gene Expression02:35

Chromatin Position Affects Gene Expression

23.7K
Chromatin is the massive complex of DNA and proteins packaged inside the nucleus. The complexity of chromatin folding and how it is packaged inside the nucleus greatly influences  access to genetic information. Generally, the nucleus' periphery is considered transcriptionally repressive, while the cell's interior is considered a transcriptionally active area. 
Topologically Associated Domains (TADs)
The 3-dimensional positioning of chromatin in the nucleus influences the...
23.7K
Nucleosome Remodeling02:54

Nucleosome Remodeling

9.5K
Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
9.5K
The Nucleosome Core Particle01:12

The Nucleosome Core Particle

1.3K
Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their primary aim is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. On the other hand, they must allow polymerase enzymes to access histone-bound DNA during...
1.3K

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 Type II CDK6 Degrader Enables Cellular Targeting beyond the Limits of Type II Inhibition.

Journal of the American Chemical Society·2026
Same author

Cleavage of MEP-1 by DPF-3 reveals novel substrate specificity and its impact on reproductive fitness.

EMBO reports·2026
Same author

Charged molecular glue discovery enabled by targeted degron display.

Nature chemical biology·2026
Same author

The E3-ome gene-centric compendium reveals the human E3 ligase landscape.

Cell·2026
Same author

Chloroplast-encoded small subunit extensions reshape the Chlamydomonas chlororibosome.

bioRxiv : the preprint server for biology·2026
Same author

The human BAF chromatin remodeler processes nucleosomes bound by pioneer transcription factors OCT4-SOX2.

Molecular cell·2026
Same journal

Genome-wide rotational and translational phasing of nucleosomes with human transcription factors.

Molecular cell·2026
Same journal

Spliceosomal proofreading factors safeguard 3' splice-site fidelity and prevent proteotoxicity and inflammation.

Molecular cell·2026
Same journal

Cytosolic EZH2-IMPDH2 complexes regulate melanoma progression and metastasis via GTP.

Molecular cell·2026
Same journal

A bacterial reverse transcriptase: Protein-templated DNA synthesis fuels antiviral immunity.

Molecular cell·2026
Same journal

Tweezing apart ribosome heterogeneity.

Molecular cell·2026
Same journal

An NADPH safety valve: De novo lipogenesis buffers biguanide-induced reductive stress.

Molecular cell·2026
查看所有相关文章

相关实验视频

Updated: Sep 13, 2025

Yeast As a Chassis for Developing Functional Assays to Study Human P53
14:57

Yeast As a Chassis for Developing Functional Assays to Study Human P53

Published on: August 4, 2019

9.6K

核细胞体指定了对p53的辅因子访问.

Deyasini Chakraborty1, Colby R Sandate2, Luke Isbel3

  • 1Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland; University of Basel, Basel, Switzerland.

Molecular cell
|July 27, 2025
PubMed
概括
此摘要是机器生成的。

染色体结构决定了哪些辅助因子可以与转录因子p53.3相互作用. 核的参与会产生选择性屏障,影响DNA损伤反应和细胞循环调节.

关键词:
基因组调节 基因组调节转录 转录 是一种转录.转录辅助因子转录辅助因子

更多相关视频

High Sensitivity Measurement of Transcription Factor-DNA Binding Affinities by Competitive Titration Using Fluorescence Microscopy
06:38

High Sensitivity Measurement of Transcription Factor-DNA Binding Affinities by Competitive Titration Using Fluorescence Microscopy

Published on: February 7, 2019

8.9K
Purification of Ubiquitinated p53 Proteins from Mammalian Cells
10:55

Purification of Ubiquitinated p53 Proteins from Mammalian Cells

Published on: March 21, 2022

2.3K

相关实验视频

Last Updated: Sep 13, 2025

Yeast As a Chassis for Developing Functional Assays to Study Human P53
14:57

Yeast As a Chassis for Developing Functional Assays to Study Human P53

Published on: August 4, 2019

9.6K
High Sensitivity Measurement of Transcription Factor-DNA Binding Affinities by Competitive Titration Using Fluorescence Microscopy
06:38

High Sensitivity Measurement of Transcription Factor-DNA Binding Affinities by Competitive Titration Using Fluorescence Microscopy

Published on: February 7, 2019

8.9K
Purification of Ubiquitinated p53 Proteins from Mammalian Cells
10:55

Purification of Ubiquitinated p53 Proteins from Mammalian Cells

Published on: March 21, 2022

2.3K

科学领域:

  • 分子生物学分子生物学
  • 染色体生物学 染色体生物学
  • 生物化学 生物化学

背景情况:

  • 先驱转录因子 (TFs) 在染色体内结合DNA基因.
  • 了解结合于核体的TF如何与辅助因子相互作用至关重要.
  • 该p53TF调节关键的细胞过程,但经常结合难以接近的色素.

研究的目的:

  • 调查染色体结合的p53与ubiquitin蛋白酶体系统 (UPS) 的辅因子的相互作用.
  • 为了确定核细胞参与如何影响与p53.3结合的辅因子.

主要方法:

  • 在体外结合测试.
  • 细胞检测. 细胞检测.
  • 电子显微镜 (cryo-EM) 结构的确定.

主要成果:

  • E3 泛基因酶E6-E6AP无法在特定的超螺旋位置 (SHL) 结合核细胞参与的p53.
  • 双基因酶USP7在体外和细胞内成功地激活了与核细胞结合的p53.
  • 一个冷EM结构揭示了USP7与p53和核细胞结合.

结论:

  • 染色素作为p53辅因子相互作用的选择性屏障.
  • 辅助因子,TFs和染色质的兼容性由灵活的相互作用领域控制.