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相关概念视频

The DNA Replication Fork01:02

The DNA Replication Fork

35.8K
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...
35.8K
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
Homologous Recombination02:31

Homologous Recombination

50.4K
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...
50.4K
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

12.5K
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
12.5K
DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

9.1K
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...
9.1K
Mismatch Repair01:20

Mismatch Repair

4.8K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
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相关实验视频

Updated: Jun 23, 2025

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

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在复制应激过程中,MRNIP限制了ssDNA间隙.

Laura G Bennett1, Ellen G Vernon1, Vithursha Thanendran1

  • 1North West Cancer Research Institute, North Wales Medical School, Bangor, Gwynedd, Wales LL57 2UW, UK.

Nucleic acids research
|June 25, 2024
PubMed
概括

MRE11调节器MRNIP在复制压力期间防止DNA缺口,特别是当叉子逆转受损时. 缺乏MRNIP会增加对PARP抑制剂和DNA损伤的敏感性.

科学领域:

  • 分子生物学分子生物学
  • 复制DNA复制DNA复制DNA复制
  • 修复DNA修复DNA的修复

背景情况:

  • 复制压力会导致DNA缺口,影响基因组的稳定性.
  • 取决于PRIMPOL的抑制会产生单链DNA (ssDNA) 缺口,与突变发生和化学敏感性有关.
  • 通过SMARCAL1和ZRANB3调解的复制分叉逆转抑制了这些差距.

研究的目的:

  • 研究MRNIP在复制压力期间调节ssDNA缺口中的作用.
  • 确定MRNIP的功能,当复制叉反转受到损害时.

主要方法:

  • 具有扰乱分叉逆转的细胞模型 (Olaparib治疗,SMARCAL1/ZRANB3耗尽).
  • 对PRIMPOL和MRE11依赖的ssDNA缺口流行率的分析.
  • 评估MRNIP缺陷细胞对PARP抑制的敏感性.
  • 研究MRNIP缺陷细胞中的填空机制.

主要成果:

  • 当叉反转受到干扰时,MRNIP限制了PRIMPOL和MRE11依赖的ssDNA间隙.
  • 缺乏MRNIP的细胞对PARP抑制具有敏感性,并积累了依赖PRIMPOL的DNA损伤.
  • 由UBC13介导的模板切换涉及REV1和Pol-ζ驱动器填补MRNIP缺陷单元中的空白.

更多相关视频

Author Spotlight: Unraveling the Dynamics of Eukaryotic DNA Replication Through Single-Molecule Visualization
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Author Spotlight: Unraveling the Dynamics of Eukaryotic DNA Replication Through Single-Molecule Visualization

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

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相关实验视频

Last Updated: Jun 23, 2025

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

Published on: February 10, 2023

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Author Spotlight: Unraveling the Dynamics of Eukaryotic DNA Replication Through Single-Molecule Visualization
07:37

Author Spotlight: Unraveling the Dynamics of Eukaryotic DNA Replication Through Single-Molecule Visualization

Published on: September 27, 2024

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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

6.1K

结论:

  • 通过调节复制后的ssDNA差距动态,MRNIP发挥了促进生存的作用.
  • 这项研究确定MRNIP是直接的MRE11调节器,调节ssDNA缺口流行.