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Mismatch Repair01:20

Mismatch Repair

5.2K
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...
5.2K
Nucleotide Excision Repair01:38

Nucleotide Excision Repair

3.8K
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...
3.8K
Spontaneous and Induced Mutations01:30

Spontaneous and Induced Mutations

152
Spontaneous mutations arise infrequently during DNA replication due to errors in the process. A key factor behind these errors is tautomeric shifts in nitrogenous bases, where bases transition from keto to enol forms or amino to imino forms. This shift can alter base-pairing rules, leading to mutations. Additionally, reactive oxygen species (ROS) arising from aerobic metabolism can damage DNA, resulting in depurination (loss of a purine base) or depyrimidination (loss of a pyrimidine base).
152
Overview of DNA Repair02:25

Overview of DNA Repair

31.6K
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.
Chemically...
31.6K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

10.2K
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...
10.2K
Homologous Recombination02:31

Homologous Recombination

52.2K
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...
52.2K

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Updated: Sep 13, 2025

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
10:59

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage

Published on: August 21, 2021

3.7K

由转录因子竞争与不匹配修复驱动的DNA突变

Wei Zhu1, Yuning Zhang2, Harshit Sahay2

  • 1Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA; Center for Advanced Genomic Technologies, Duke University, Durham, NC 27708, USA.

Cell
|July 30, 2025
PubMed
概括

转录因子 (TF) 可以通过干扰不匹配修复 (MMR) 来促进DNA突变. 这种TF-MMR竞争机制解释了酵母和人类癌症中TF结合点的突变模式,影响了基因组进化.

关键词:
DNA不匹配的修复基因突变DNA复制错误没有.竞争与不匹配的修复过度突变突变模式转录因子结合部位的突变转录因子

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Application of Stopped-flow Kinetics Methods to Investigate the Mechanism of Action of a DNA Repair Protein
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Application of Stopped-flow Kinetics Methods to Investigate the Mechanism of Action of a DNA Repair Protein

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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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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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相关实验视频

Last Updated: Sep 13, 2025

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
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Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage

Published on: August 21, 2021

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Application of Stopped-flow Kinetics Methods to Investigate the Mechanism of Action of a DNA Repair Protein
11:01

Application of Stopped-flow Kinetics Methods to Investigate the Mechanism of Action of a DNA Repair Protein

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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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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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科学领域:

  • 分子生物学
  • 遗传学
  • 基因组学

背景情况:

  • 细胞DNA复制非常准确,但仍然会产生突变.
  • 突变是由于复制过程中的核酸错误结合引起的.
  • 这些错误有助于遗传疾病和基因组进化.

研究的目的:

  • 研究转录因子 (TF) 如何影响突变率.
  • 阐明TF诱导的突变发生的分子机制.
  • 了解TF-MMR竞争在癌症和基因组进化中的作用.

主要方法:

  • 使用酵母基因分析量化TF结合部位的突变.
  • 分析了人类癌症基因组中的突变模式.
  • 调查了TFs和MutSα (MMR发起者) 在DNA不匹配识别方面的竞争.

主要成果:

  • 转录因子通过阻碍不匹配修复 (MMR) 来增加突变发生.
  • 在酵母TF结合部位中观察到TF诱导的突变发生.
  • 人类癌症突变数据显示MMR熟练细胞中MYC结合不匹配的突变丰富.

结论:

  • TF-MMR竞争是癌症中TF结合位点体质突变的一个关键驱动因素.
  • 这种机制解释了TF结合部位的高突变率.
  • 这些发现对理解调节性DNA进化有重要意义.