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

The DNA Replication Fork01:02

The DNA Replication Fork

35.6K
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...
35.6K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

9.8K
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...
9.8K
Homologous Recombination02:31

Homologous Recombination

50.2K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
50.2K
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
DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

9.0K
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...
9.0K
Replication in Prokaryotes01:32

Replication in Prokaryotes

24.3K
DNA replication has three main steps: initiation, elongation, and termination. Replication in prokaryotes begins when initiator proteins bind to the single origin of replication (ori) on the cell's circular chromosome. Replication then proceeds around the entire circle of the chromosome in each direction from the two replication forks, resulting in two DNA molecules.
Many Proteins Work Together to Replicate the Chromosome
Replication is coordinated and carried out by a host of specialized...
24.3K

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

Experimental evolution of cellular miniaturization reveals a putative mechanism for cell size evolution.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Experimental evolution of cellular miniaturization reveals a mechanism for cell size evolution.

bioRxiv : the preprint server for biology·2025
Same author

Model-based inference of cell cycle dynamics captures alterations of the DNA replication programme.

PLoS computational biology·2025
Same author

Compensatory evolution to DNA replication stress is robust to nutrient availability.

Molecular systems biology·2025
Same author

Experimental approaches to study evolutionary cell biology using yeasts.

Yeast (Chichester, England)·2023
Same author

Ploidy and recombination proficiency shape the evolutionary adaptation to constitutive DNA replication stress.

PLoS genetics·2021

相关实验视频

Updated: Jun 7, 2025

Quantifying Replication Stress in Ovarian Cancer Cells Using Single-Stranded DNA Immunofluorescence
06:25

Quantifying Replication Stress in Ovarian Cancer Cells Using Single-Stranded DNA Immunofluorescence

Published on: February 10, 2023

2.0K

对DNA复制的补偿进化 压力对营养素的可用性是坚固的

Mariana Natalino1, Marco Fumasoni1

  • 1Gulbenkian Institute for Molecular Medicine (GIMM), Lisbon, Portugal.

bioRxiv : the preprint server for biology
|November 18, 2024
PubMed
概括

在DNA复制压力之后的进化修复在环境中是可以预测的. 确定了赋予健身优势的反复突变,揭示了强大的适应机制,对基因组稳定性和癌症研究产生影响.

科学领域:

  • 进化生物学 进化生物学
  • 遗传学 是一个遗传学.
  • 分子生物学分子生物学

背景情况:

  • 进化修复描述了细胞过程中断后的补偿进化.
  • 基因型与环境的相互作用可以塑造进化轨迹.
  • DNA复制压力会导致遗传不稳定,损害DNA合成.

研究的目的:

  • 为了测试在DNA复制压力下进化修复的可预测性.
  • 为了研究葡萄糖可用性对适应的影响.
  • 为了确定基因机制的基础适应复制压力.

主要方法:

  • 在构成性复制压力下*Saccharomyces cerevisiae*的高通量实验进化.
  • 在不同的葡萄糖度下生长,以评估环境影响.
  • 分析反复发生的突变及其在不同环境中的适应性影响.

主要成果:

  • 葡萄糖水平影响了生理和适应率,但并没有影响适应基因的强度.
  • 经常发生的突变在不同的葡萄糖可用性中始终改善了健康状况.
  • 在适应过程中发现了RNA聚合酶II的媒介复合物的新型作用.

更多相关视频

Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
08:53

Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method

Published on: May 2, 2025

275
Detection of Post-Replicative Gaps Accumulation and Repair in Human Cells Using the DNA Fiber Assay
10:32

Detection of Post-Replicative Gaps Accumulation and Repair in Human Cells Using the DNA Fiber Assay

Published on: February 3, 2022

6.0K

相关实验视频

Last Updated: Jun 7, 2025

Quantifying Replication Stress in Ovarian Cancer Cells Using Single-Stranded DNA Immunofluorescence
06:25

Quantifying Replication Stress in Ovarian Cancer Cells Using Single-Stranded DNA Immunofluorescence

Published on: February 10, 2023

2.0K
Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
08:53

Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method

Published on: May 2, 2025

275
Detection of Post-Replicative Gaps Accumulation and Repair in Human Cells Using the DNA Fiber Assay
10:32

Detection of Post-Replicative Gaps Accumulation and Repair in Human Cells Using the DNA Fiber Assay

Published on: February 3, 2022

6.0K

结论:

  • 进化修复DNA复制压力是强大的和可预测的.
  • 适应机制在很大程度上独立于宏观营养素的可用性.
  • 这些发现提供了对基因组稳定性和与癌症发展的潜在联系的见解.