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相关概念视频

Replication in Eukaryotes01:29

Replication in Eukaryotes

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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...
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The DNA Replication Fork01:02

The DNA Replication Fork

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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...
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DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

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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...
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Replication in Prokaryotes01:32

Replication in Prokaryotes

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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...
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S-Cdk Initiates DNA Replication02:38

S-Cdk Initiates DNA Replication

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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
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Genome Copying Errors02:46

Genome Copying Errors

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DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
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相关实验视频

Updated: Jun 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

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在DNA复制时间程序出现时胚胎基因组不稳定

Saori Takahashi1, Hirohisa Kyogoku2,3, Takuya Hayakawa4

  • 1Laboratory for Developmental Epigenetics, RIKEN Center for Biosystems Dynamics Research (BDR), Kobe, Japan.

Nature
|August 28, 2024
PubMed
概括
此摘要是机器生成的。

早期的小鼠胚胎由于DNA复制不协调而出现了暂时的基因组不稳定. 这种不稳定性,以缓慢的复制分叉和DNA损伤为标志,由8细胞阶段解决,确保基因组完整性.

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Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
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Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization

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G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome
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相关实验视频

Last Updated: Jun 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

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

Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization

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

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科学领域:

  • 发育生物学
  • 遗传学
  • 分子生物学

背景情况:

  • 为了保持基因组完整性,忠实的DNA复制是至关重要的.
  • 在早期胚胎生成中观察到复制缺陷和染色体分离错误.
  • 早期哺乳动物胚胎中的DNA复制的调节还不清楚.

研究的目的:

  • 在单细胞水平上研究植入前小鼠胚胎中的DNA复制程序.
  • 在早期发育过程中识别基因组不稳定的关键时期.
  • 了解复制时间和分叉进展之间的协调.

主要方法:

  • 在小鼠胚胎中构建单细胞全基因组DNA复制图谱.
  • 对复制时间程序和复制分叉速度的分析.
  • 对复制压力,DNA损伤和染色体分离错误的评估.

主要成果:

  • 早期的胚胎 (1-2 细胞) 缺乏复制时间程序,复制速度缓慢且均.
  • 一个体状的复制程序开始于4细胞阶段,但具有缓慢的分叉和增加的复制压力.
  • 破裂型染色体分离错误发生在4至8个细胞分裂期间,与晚复制区域相关.
  • 通过加快分叉速度和减少压力, 核酸补充可以挽救错误.
  • 在8细胞阶段,复制动态正常化,染色体异常减少.

结论:

  • 在正常小鼠发育过程中发生过渡性基因组不稳定期.
  • 这种不稳定性与S阶段早期的复制时间和分叉调节之间缺乏协调有关.
  • 复制过程的协调对于在胚胎发生过程中保持基因组稳定至关重要.