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

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
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
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

10.1K
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...
10.1K
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
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
Spontaneous and Induced Mutations01:30

Spontaneous and Induced Mutations

143
Spontaneous mutations arise infrequently during DNA replication due to errors in the process. A key factor behind these errors is tautomeric shifts in nitrogenous bases, where bases transition from keto to enol forms or amino to imino forms. This shift can alter base-pairing rules, leading to mutations. Additionally, reactive oxygen species (ROS) arising from aerobic metabolism can damage DNA, resulting in depurination (loss of a purine base) or depyrimidination (loss of a pyrimidine base).
143

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

The Fanconi anemia pathway repairs colibactin-induced DNA interstrand cross-links.

Nature communications·2025
Same author

PARP1 auto-modification promotes faithful Okazaki fragment processing and limits replication fork speed.

Molecular cell·2025
Same author

CRAMP1-dependent histone H1 biogenesis is essential for topoisomerase II inhibitor tolerance.

Molecular cell·2025
Same author

Quantitative Chromatin Protein Dynamics During Replication Origin Firing in Human Cells.

Molecular & cellular proteomics : MCP·2025
Same author

Catalytic and noncatalytic functions of DNA polymerase κ in translesion DNA synthesis.

Nature structural & molecular biology·2024
Same author

PARP1-dependent DNA-protein crosslink repair.

Nature communications·2024

相关实验视频

Updated: Sep 10, 2025

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
10:59

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage

Published on: August 21, 2021

3.7K

只是绕过它:DNA损伤耐受性的机制

Sidak Minocha1, Marta Oliva-Santiago1, Sampath Amitash Gadi1

  • 1Biotech Research and Innovation Center, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2200, Copenhagen, Denmark; Novo Nordisk Foundation Center for Protein Research, University of Copenhagen, Copenhagen, Denmark.

Trends in biochemical sciences
|August 22, 2025
PubMed
概括

通过绕过病变来确保基因组重复的DNA损伤耐受机制. 这篇评论涵盖了转化DNA合成,模板切换和复制叉动态,突出了DNA修复中的未解决问题.

关键词:
DNA复制在PCNA无处不在翻转叉子镇压模板切换转化合成

更多相关视频

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
Author Spotlight: Combining Proximity Ligand Assay with Gamma-H2AX Staining to Characterize Protein Interactions in DNA Damage Response
09:39

Author Spotlight: Combining Proximity Ligand Assay with Gamma-H2AX Staining to Characterize Protein Interactions in DNA Damage Response

Published on: August 2, 2024

586

相关实验视频

Last Updated: Sep 10, 2025

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
10:59

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage

Published on: August 21, 2021

3.7K
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
Author Spotlight: Combining Proximity Ligand Assay with Gamma-H2AX Staining to Characterize Protein Interactions in DNA Damage Response
09:39

Author Spotlight: Combining Proximity Ligand Assay with Gamma-H2AX Staining to Characterize Protein Interactions in DNA Damage Response

Published on: August 2, 2024

586

科学领域:

  • 分子生物学
  • 遗传学
  • 生物化学

背景情况:

  • DNA 损伤对复制基因组构成重大威胁.
  • DNA损伤耐受性 (DDT) 机制对于完整的基因组复制至关重要.
  • 主要的DDT途径包括转化DNA合成 (TLS) 和模板切换.

研究的目的:

  • 让我们回顾一下DNA损伤的基本概念.
  • 整合该领域的最新进展.
  • 识别和突出未解决的问题在DNA损伤耐受性.

主要方法:

  • 对DNA复制和修复的最新进展进行文献审查.
  • 分析促进病变绕道的机制,包括TLS和模板切换.
  • 检查复制叉反转和抑制的作用.

主要成果:

  • DNA聚合酶可以通过TLS或模板切换绕过病变.
  • 复制分叉动力学,如逆转和抑制,对于病变绕道至关重要.
  • 尽管经过几十年的研究, 这些过程的基本方面仍然不清楚.

结论:

  • DNA损伤耐受性是一个复杂的过程,
  • 需要进一步研究以充分阐明病变绕道及其调节的复杂性.
  • 了解这些途径对于基因组稳定性和疾病预防至关重要.