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

Nucleotide Excision Repair01:38

Nucleotide Excision Repair

3.8K
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
3.8K
DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

9.3K
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...
9.3K
Base Excision Repair01:54

Base Excision Repair

22.9K
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
22.9K
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

12.9K
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
12.9K
Epigenetic Regulation01:37

Epigenetic Regulation

3.1K
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
3.1K
Overview of DNA Repair02:25

Overview of DNA Repair

31.6K
In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
31.6K

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

CD47 monoclonal antibody enhances the inhibitory effect of anti-HER2 chimeric antigen receptor macrophages on ovarian cancer.

Oncology letters·2026
Same author

Performance and reproducibility of Pylori DuoTect® in a high Helicobacter pylori prevalence Latin American population.

Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi·2026
Same author

Intravital calcium imaging of meningeal macrophages reveals niche-specific dynamics and aberrant responses to brain hyperexcitability.

eLife·2026
Same author

The P2X4-P2X7 purinergic axis in alcohol-related liver disease: from fibrogenesis to immunotherapy resistance.

Purinergic signalling·2026
Same author

Optimizing next-generation CAR-macrophages against solid tumors: challenges and potential strategies.

Journal of hematology & oncology·2026
Same author

Anti-Epstein-Barr virus (EBV) antibodies in EBV-associated gastric carcinoma.

Infectious agents and cancer·2026

相关实验视频

Updated: Sep 10, 2025

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
09:42

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images

Published on: September 7, 2017

9.8K

通过甲基转移酶SETD6的RAD18甲基化减弱了DNA断裂

Lital Estrella Weil1, Michal Feldman1, Jennifer Van Duine2

  • 1The Shraga Segal Department of Microbiology, Immunology and Genetics, Ben-Gurion University of the Negev, P.O.B. 653, Be'er-Sheva, 84105, Israel.

Scientific reports
|August 27, 2025
PubMed
概括
此摘要是机器生成的。

甲基转移酶SETD6与DNA修复蛋白RAD18相互作用并进行甲基化. 这种甲基化调节RAD18

更多相关视频

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
06:59

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter

Published on: March 31, 2022

2.5K
Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage
10:44

Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage

Published on: January 31, 2018

10.4K

相关实验视频

Last Updated: Sep 10, 2025

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
09:42

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images

Published on: September 7, 2017

9.8K
Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
06:59

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter

Published on: March 31, 2022

2.5K
Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage
10:44

Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage

Published on: January 31, 2018

10.4K

科学领域:

  • 分子生物学
  • 表观遗传学
  • DNA 修复机制

背景情况:

  • SETD6是一种含有SET域的甲基转移酶,参与后翻译性修饰.
  • RAD18是DNA损伤修复途径中的关键蛋白质.
  • 蛋白质甲基化调节蛋白质的功能,稳定性和相互作用.

研究的目的:

  • 研究SETD6和RAD18之间的相互作用.
  • 要确定SETD6是否甲基化RAD18,并阐明这种修改的功能后果.
  • 了解SETD6介导的RAD18甲基化在维持基因组完整性的作用.

主要方法:

  • 蛋白质微阵列技术用于识别反应器.
  • 通过ELISA和免疫沉测试来确认相互作用和甲基化.
  • 质谱和位点定向的突变生成以确定甲基化位点.
  • 在SETD6淘汰细胞中分析DNA损伤标记 (γH2AX) 和彗星测定.

主要成果:

  • RAD18被确定为SETD6的直接相互作用者和基质.
  • 通过SETD6对K73和K406残留物进行单甲基化.
  • 通过SETD6介导的甲基化会影响RAD18的核定位.
  • 减少SETD6导致DNA损伤标志物增加和DNA断裂.

结论:

  • 通过SETD6介导的RAD18甲基化对于减弱DNA断裂至关重要.
  • 这种甲基化调节RAD18的细胞局部化和功能.
  • 通过RAD18调节,SETD6在保持基因组完整性方面发挥着关键作用.