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Genome Copying Errors02:46

Genome Copying Errors

4.3K
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.
4.3K
The DNA Replication Fork01:02

The DNA Replication Fork

36.5K
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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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,...
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Chromosome Replication02:31

Chromosome Replication

9.0K
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...
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Replication in Eukaryotes01:29

Replication in Eukaryotes

14.2K
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...
14.2K
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

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Updated: Aug 28, 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

8.5K

複製のタイミングと遺伝的不安定性

Marcel Méchali1

  • 1Institute of Human Genetics, CNRS-University of Montpellier, Montpellier, France.

Science (New York, N.Y.)
|September 15, 2022
PubMed
まとめ
この要約は機械生成です。

DNA複製の起源の同期した活性化はリンパ腫の遺伝的不安定性を引き起こします この発見は,がんの発生と進行に寄与する重要なメカニズムを強調しています.

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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

14.0K
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

関連する実験動画

Last Updated: Aug 28, 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

8.5K
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

14.0K
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

科学分野:

  • 遺伝学
  • 分子生物学
  • 癌 研究

背景:

  • 遺伝子の不安定さは リンパ腫を含む癌の特徴です
  • DNA複製の調節不良は,様々な癌の発生に関与している.

研究 の 目的:

  • リンパ腫における同期DNA複製起源活性化の役割を調査する.
  • リンパ腫細胞の複製のタイミングと 遺伝的不安定性の関係を理解する

主な方法:

  • リンパ腫細胞系におけるDNA複製原発をモニタリングする技術を用いた.
  • 同期複製イベントに関連したゲノム変異を分析した.

主要な成果:

  • DNA複製の起源の同期活性化により DNAの断裂が増加することが示された.
  • リンパ腫の異常発症と 特定のタイプの遺伝的不安定性との相関が観察されました

結論:

  • シンクロナイズドDNA複製起源の活性化は,リンパ腫における遺伝的不安定性の重要な要因である.
  • リプリケーションのタイミングをターゲットにすることで,リンパ腫の治療に新しい治療戦略を提供することができます.