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

36.8K
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...
36.8K
S-Cdk Initiates DNA Replication02:38

S-Cdk Initiates DNA Replication

4.8K
The cell cycle is a series of events leading to DNA duplication followed by the division of cell content to form two daughter cells. The cell cycle progresses in four stages—the cell increases in size (gap 1 or G1-phase), duplicates its DNA (synthesis or S-phase), prepares to divide (gap 2 or G2-phase), and divides (mitosis or M-phase).
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of...
4.8K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.9K
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,...
5.9K
Chromosome Replication02:31

Chromosome Replication

9.1K
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...
9.1K
Replication in Prokaryotes01:32

Replication in Prokaryotes

25.3K
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...
25.3K
Replication in Eukaryotes01:29

Replication in Eukaryotes

14.6K
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...
14.6K

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

Mucin-derived sugars act as metabolic brakes controlling growth initiation in <i>Akkermansia muciniphila</i>.

Gut microbes·2026
Same author

TlyA is a 23S and 16S 2'-O-methylcytidine methyltransferase important for ribosome assembly in Bacillus subtilis.

Nucleic acids research·2026
Same author

Single-molecule tracking of RNA-DNA hybrid removal enzymes important for lagging-strand replication.

bioRxiv : the preprint server for biology·2025
Same author

<i>Bacillus subtilis</i> RNase HII is inefficient at processing guanosine monophosphate and damaged ribonucleotides.

bioRxiv : the preprint server for biology·2025
Same author

Control of <i>Clostridioides difficile</i> virulence and physiology by the flagellin homeostasis checkpoint FliC-FliW-CsrA in the absence of motility.

mBio·2025
Same author

Two distinct regulatory systems control pulcherrimin biosynthesis in Bacillus subtilis.

PLoS genetics·2024

相关实验视频

Updated: Sep 14, 2025

Genome-wide Determination of Mammalian Replication Timing by DNA Content Measurement
08:06

Genome-wide Determination of Mammalian Replication Timing by DNA Content Measurement

Published on: January 19, 2017

8.6K

基因复制启动时间对于保持基因组完整性很重要.

Tristan T Reed1, Abigail H Kendal1, Katherine J Wozniak1

  • 1Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan, USA.

Journal of bacteriology
|July 21, 2025
PubMed
概括

调节DNA复制启动对于基因组稳定性至关重要. 在Bacillus subtilis中,DNA复制的低启动和过度启动都增加了对DNA损伤的敏感性,影响了修复效率.

科学领域:

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

背景情况:

  • 基因复制的启动受到积极和消极因素的严格调节.
  • 改变复制启动频率对细菌基因组稳定性的影响尚不清楚.
  • YabA充当负调节剂,而CcrZ充当Bacillus subtilis.复制启动的正调节剂.

研究的目的:

  • 为了研究DNA复制的后果低启动和过度启动对细菌细菌的基因组稳定性.
  • 为了确定复制启动频率与对基因毒性压力的敏感性之间的关系.
  • 阐明基因组不稳定性背后的机制,由改变的复制启动引起.

主要方法:

  • 测量源到终点比作为复制启动活动的代理.
  • 分析ReCA-GFP焦点形成以评估复制叉压力.
  • 评估对mitomycin C的敏感性,以确定基因毒性应激反应.

主要成果:

  • 删除ccrZ或特定ccrZ等位基因导致DNA复制的启动不足.
  • 消去yaba或crz过度生产导致复制过度启动.
  • 低启动和过度启动的细胞都对米托米辛C敏感度增加,这表明DNA修复能力受到损害.
关键词:
这种细菌是 Bacillus subtilis.CcrZ CcrZ 在线阅读复制DNA复制DNA复制DNA复制DnaAA DnaA 是一个这里是ReCAA.

更多相关视频

G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome
06:40

G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome

Published on: March 22, 2018

5.9K
Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
17:14

Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization

Published on: December 10, 2012

14.1K

相关实验视频

Last Updated: Sep 14, 2025

Genome-wide Determination of Mammalian Replication Timing by DNA Content Measurement
08:06

Genome-wide Determination of Mammalian Replication Timing by DNA Content Measurement

Published on: January 19, 2017

8.6K
G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome
06:40

G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome

Published on: March 22, 2018

5.9K
Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
17:14

Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization

Published on: December 10, 2012

14.1K

结论:

  • 严格调节DNA复制启动对于保持细菌基因组完整性至关重要.
  • 低启动导致通过异步复制和低效的同源重组导致敏感性.
  • 过度启动会导致复制叉压力,加剧DNA损伤的敏感性.