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相关概念视频

DNA Damage can Stall the Cell Cycle02:37

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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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Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
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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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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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Overview of DNA Repair

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In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
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Nucleotide Excision Repair

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DNA Distortion and Damage
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代码中的错误:结核病阻止了DNA修复.

Bala T S A Madduri1, Samantha L Bell2

  • 1Center for Emerging & Re-emerging Pathogens, Rutgers New Jersey Medical School, Newark, NJ, USA; Department of Medicine, Rutgers New Jersey Medical School, Newark, NJ, USA.

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概括
此摘要是机器生成的。

结核菌菌的感染会损害宿主细胞的DNA. 一种分泌的蛋白质抑制了DNA修复,通过利用这种遗传损伤促进了细菌的复制.

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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:

  • 细胞基因组完整性对于生存至关重要.
  • 传染剂可以造成DNA损伤,从而损害遗传稳定性.
  • 了解利用宿主DNA损伤的病原体机制至关重要.

研究的目的:

  • 为了研究Mycobacterium结核病如何利用宿主DNA损伤.
  • 为了确定参与操纵DNA修复途径的细菌因素.
  • 为了阐明DNA损伤和M.结核病复制之间的联系.

主要方法:

  • 在M.结核病感染期间对宿主-病原体相互作用的分析.
  • 研究分泌蛋白质在调节宿主DNA修复中的作用.
  • 评估DNA修复抑制对细菌生存和复制的影响.

主要成果:

  • 结核菌菌分泌一种蛋白质,干扰宿主DNA修复机制.
  • 抑制DNA修复创造了一个有利于细菌繁殖的细胞环境.
  • 病原体积极利用受损的遗传完整性为自己的利益.

结论:

  • 结核菌拥有复杂的策略来操纵宿主细胞过程.
  • 利用DNA损伤和抑制修复是关键的毒性因素.
  • 针对这些机制可以提供针对结核病的新型治疗策略.