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相关概念视频

Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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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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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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Nucleotide Excision Repair01:38

Nucleotide Excision Repair

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DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
3.5K
Homologous Recombination02:31

Homologous Recombination

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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...
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The DNA Replication Fork01:02

The DNA Replication Fork

35.7K
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...
35.7K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

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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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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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引起HPV的R环形成抑制了先天免疫基因表达,同时激活了DNA损伤修复途径.

Conor W Templeton1, Laimonis A Laimins1

  • 1Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America.

PLoS pathogens
|August 23, 2024
PubMed
概括

异常的R环在HPV阳性宫细胞中升高,改变基因转录和免疫通路. 这些发现将R环与DNA修复和HPV病变发生过程中的免疫调节联系起来.

科学领域:

  • 分子生物学分子生物学
  • 基因组学就是基因组学.
  • 癌症研究 癌症研究

背景情况:

  • R环,三元核酸结构,调节转录和复制.
  • 异常的R循环可以导致DNA断裂和基因组不稳定.
  • 在癌症和受人类乳头瘤病毒 (HPV) 感染的细胞中观察到升高的R环.

研究的目的:

  • 为了研究正常角质细胞和HPV阳性宫内皮质瘤 (CIN I) 细胞之间的R环分布和功能的变化.
  • 了解增强R环对HPV阳性细胞中的基因转录和相关途径的影响.

主要方法:

  • 对正常角质细胞中的R环水平与HPV阳性CIN I细胞的比较分析.
  • 评估基因转录变化对R环存在的反应.
  • 在R环,基因素修饰 (H3K36me3, γH2AX) 和基因表达路径之间进行相关性分析.

主要成果:

  • 细胞基因中的R环水平高达10倍,HPV阳性细胞中的ALU1元素高达500倍.
  • 增强的R循环导致基因转录发生变化,观察到增加和减少,影响诸如先天性免疫和DNA损伤修复等途径.
  • 天生的免疫基因 (例如DDX58,IL-6) 的降低调节和DNA损伤修复基因 (例如ATM,ATRX) 的上调调节与HPV阳性细胞中的R循环和特定基因素标记有关.

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Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
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Author Spotlight: Decoding DNA Repair by Extrachromosomal NHEJ Assay and HR Assays
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Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
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Author Spotlight: Decoding DNA Repair by Extrachromosomal NHEJ Assay and HR Assays
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Author Spotlight: Decoding DNA Repair by Extrachromosomal NHEJ Assay and HR Assays

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结论:

  • HPV 感染显著增加了宫细胞中的 R 环形成,影响了基因表达.
  • 在R环,DNA损伤修复和HPV阳性细胞的先天免疫路径之间存在潜在的联系.
  • 这些与R循环相关的变化可能在HPV病原和疾病进展中发挥关键作用.