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相关概念视频

Homologous Recombination02:31

Homologous Recombination

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...
Homologous Recombination02:31

Homologous Recombination

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...
Cohesins02:20

Cohesins

Cohesin protein complexes are a molecular glue that holds two sister chromatids together. They play an important role both in mitosis and meiosis. In mitosis, all cohesin complexes present on the chromosomes are removed before the start of the anaphase stage.
Cohesin complexes in Meiotic Division
Meiosis involves two distinct rounds of chromosomal segregation and cell divisions— Meiosis I followed by Meiosis II – producing four daughter cells. Meiosis I includes the separation of homologous...
Cohesins02:20

Cohesins

Cohesin protein complexes are a molecular glue that holds two sister chromatids together. They play an important role both in mitosis and meiosis. In mitosis, all cohesin complexes present on the chromosomes are removed before the start of the anaphase stage.
Cohesin complexes in Meiotic Division
Meiosis involves two distinct rounds of chromosomal segregation and cell divisions— Meiosis I followed by Meiosis II – producing four daughter cells. Meiosis I includes the separation of homologous...
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

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...
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

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...

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相关实验视频

Updated: Jul 13, 2026

Visualization of miniSOG Tagged DNA Repair Proteins in Combination with Electron Spectroscopic Imaging (ESI)
13:06

Visualization of miniSOG Tagged DNA Repair Proteins in Combination with Electron Spectroscopic Imaging (ESI)

Published on: September 24, 2015

通过Eco1 (Ctf7) 引发全基因组姐妹染色体凝聚力的DNA双链断裂.

Elçin Unal1, Jill M Heidinger-Pauli, Douglas Koshland

  • 1Carnegie Institution, Howard Hughes Medical Institute, Department of Embryology, 3520 San Martin Drive, Baltimore, MD 21218, USA.

Science (New York, N.Y.)
|July 14, 2007
PubMed
概括

通过Eco1 (Ctf7) 通过DNA双链断裂 (DSB) 独立于DNA复制建立姐妹染色体凝聚力. 这一过程保护了全基因组的染色体完整性.

科学领域:

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

背景情况:

  • 凝聚素调解姐妹染色体凝聚力,这对于忠实染色体分离和DNA双链断裂 (DSB) 修复至关重要.
  • 传统上,人们认为凝聚力建立仅在DNA复制过程中发生,与复制体和Eco1 (Ctf7) 相结合.

研究的目的:

  • 研究DNA复制之外的DSB响应凝聚力生成的机制.
  • 阐明Eco1 (Ctf7) 在凝聚力和DNA损伤反应中的双重功能.

主要方法:

  • 用了开花酵母作为模型生物.
  • 调查Eco1 (Ctf7) 活动和凝聚力建立,以响应G2/M阶段的DSB.
  • 分析了Eco1的乙转移酶活性和DNA损伤检查点的作用.

主要成果:

  • 证明Eco1 (Ctf7) 依赖的,复制独立的凝聚力产生,以响应G2/M的DSB.
  • 确定了Eco1 (Ctf7) 的两个不同的功能:直接建立凝聚力和通过其乙转移酶活性触发凝聚力,以应对DSB和DNA损伤检查点.
  • 观察到DSB诱导的结合在破碎和不破碎的染色体上.

结论:

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Visualization of DNA Repair Proteins Interaction by Immunofluorescence
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Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage
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Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage

Published on: January 31, 2018

相关实验视频

Last Updated: Jul 13, 2026

Visualization of miniSOG Tagged DNA Repair Proteins in Combination with Electron Spectroscopic Imaging (ESI)
13:06

Visualization of miniSOG Tagged DNA Repair Proteins in Combination with Electron Spectroscopic Imaging (ESI)

Published on: September 24, 2015

Visualization of DNA Repair Proteins Interaction by Immunofluorescence
07:55

Visualization of DNA Repair Proteins Interaction by Immunofluorescence

Published on: June 26, 2020

Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage
10:44

Laser Microirradiation to Study In Vivo Cellular Responses to Simple and Complex DNA Damage

Published on: January 31, 2018

  • 通过展示凝聚力可以独立于复制而建立,挑战了既定的模型.
  • 突出了Eco1 (Ctf7) 在基因组稳定中的双重作用,将DSB修复和DNA损伤检查点联系起来.
  • 建议通过Eco1 (Ctf7) 作用的DNA损伤检查点提供全基因组对染色体完整性的保护.