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

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
The DNA Replication Fork01:02

The DNA Replication Fork

36.0K
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...
36.0K
Chromosome Replication02:31

Chromosome Replication

8.7K
Before a cell can divide, it must accurately replicate all of its chromosomes, including the DNA and its associated histone and non-histone proteins.  This process begins at numerous origins of replication during the S phase of the cell cycle in each of a cell’s chromosomes simultaneously. Certain nucleotides can act as origins of replication, but these sequences are not well defined - especially in complex, multi-cellular, eukaryotic species. The length of DNA that spans an origin...
8.7K
Replication in Eukaryotes01:29

Replication in Eukaryotes

13.8K
In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
13.8K
Homologous Recombination02:31

Homologous Recombination

50.5K
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...
50.5K
Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

6.2K
Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
6.2K

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

H2BE113K mutation promotes breast cancer metastasis through modulating chromatin dynamics.

Science advances·2026
Same author

Pyruvate leaves its mark on chromatin.

Nature metabolism·2026
Same author

Author Correction: DNA-guided CRISPR-Cas12a effectors for programmable RNA recognition and cleavage.

Nature biotechnology·2026
Same author

Distinct roles of MCM2-7 subunits in replication licensing in human cells.

Nature communications·2026
Same author

Structural basis for prohibitin-mediated regulation of mitochondrial m-AAA protease.

Nature communications·2026
Same author

DNA-guided CRISPR-Cas12a effectors for programmable RNA recognition and cleavage.

Nature biotechnology·2026

相关实验视频

Updated: Jul 1, 2025

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

351

在复制分叉中捕获的亲基素转移

Ningning Li1, Yuan Gao2, Yujie Zhang3

  • 1State Key Laboratory of Membrane Biology, Peking-Tsinghua Center for Life Sciences, School of Life Sciences, Peking University, Beijing, China.

Nature
|March 6, 2024
PubMed
概括

研究人员可视化了FACT复合体和被驱逐的基因组如何与酵母复合体相互作用. 这揭示了对复制合基因子循环的结构性见解,这对于在DNA复制过程中维持表观遗传至关重要.

更多相关视频

Examination of Proteins Bound to Nascent DNA in Mammalian Cells Using BrdU-ChIP-Slot-Western Technique
09:14

Examination of Proteins Bound to Nascent DNA in Mammalian Cells Using BrdU-ChIP-Slot-Western Technique

Published on: January 14, 2016

9.2K
Visualization of DNA Replication in the Vertebrate Model System DT40 using the DNA Fiber Technique
07:18

Visualization of DNA Replication in the Vertebrate Model System DT40 using the DNA Fiber Technique

Published on: October 27, 2011

39.9K

相关实验视频

Last Updated: Jul 1, 2025

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

351
Examination of Proteins Bound to Nascent DNA in Mammalian Cells Using BrdU-ChIP-Slot-Western Technique
09:14

Examination of Proteins Bound to Nascent DNA in Mammalian Cells Using BrdU-ChIP-Slot-Western Technique

Published on: January 14, 2016

9.2K
Visualization of DNA Replication in the Vertebrate Model System DT40 using the DNA Fiber Technique
07:18

Visualization of DNA Replication in the Vertebrate Model System DT40 using the DNA Fiber Technique

Published on: October 27, 2011

39.9K

科学领域:

  • 分子生物学
  • 表观遗传学
  • 结构生物学

背景情况:

  • 细胞的DNA通过核体被压缩成染色体.
  • 基因组复制需要对表观基因组进行协调传输.
  • 了解复制过程中的基因组动态是表观遗传的关键.

研究的目的:

  • 通过FACT复合物在DNA复制过程中确定基因组管理的结构机制.
  • 为了阐明被排斥的基因组是如何被复合体处理和回收的.

主要方法:

  • 酵母复制体的冷电子显微镜 (冷EM).
  • 对FACT复合体 (Spt16,Pob3) 与被驱逐的基因组相互作用的结构分析.
  • 对Mcm2基因组结合域相互作用的可视化.

主要成果:

  • 在复合体前面捕获被驱逐的基因组.
  • 麦克米2与H3-H4四聚合物结合,占据一个空缺的H2A-H2B位点.
  • 基因组重新定位以转移到新合成的DNA,从而促进基因组循环.

结论:

  • 提供对复制合基因组循环的关键结构见解.
  • 在DNA复制过程中保持表观遗传信息的机制.
  • 突出了FACT和Mcm2在复制过程中的组织蛋白管理中的作用.