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相关概念视频

Mismatch Repair01:20

Mismatch Repair

4.9K
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...
4.9K
Homologous Recombination02:31

Homologous Recombination

50.7K
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...
50.7K
Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

7.1K
Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
7.1K
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

12.7K
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...
12.7K
Base Excision Repair01:54

Base Excision Repair

22.7K
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
22.7K
Proofreading01:31

Proofreading

6.4K
Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase...
6.4K

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相关实验视频

Updated: Jul 28, 2025

Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers
08:48

Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers

Published on: October 13, 2011

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提取短DNA与不匹配的基对.

Navin Singh1, Nehal Mathur2

  • 1Department of Physics, Birla Institute of Technology and Science, Pilani, Rajasthan, 333 031, India. navin@pilani.bits-pilani.ac.in.

European biophysics journal : EBJ
|May 30, 2023
PubMed
概括

DNA 缺陷会影响基因表达的准确性. 这项研究揭示了具有缺陷的DNA在较低温度下变质,并在热与力合并中表现出不同的行为.

科学领域:

  • 分子生物学分子生物学
  • 生物物理学的生物物理.
  • 遗传学 是一个遗传学.

背景情况:

  • 基因复制错误可能导致DNA分子缺陷.
  • 这些DNA缺陷可能会影响基因表达的准确性.

研究的目的:

  • 为了研究不同数量的缺陷 (2-16) 的DNA的稳定性.
  • 为了比较热和力合集中的DNA变性过程.

主要方法:

  • 使用统计模型计算DNA点.
  • 分析了不同缺陷度的DNA稳定性.

主要成果:

  • 与完整的DNA相比,有缺陷的DNA在较低的温度下变质.
  • 热和力组合之间的变质模式显著不同.
  • 拉动点是力量组合中的DNA变性的一个关键因素.

结论:

  • DNA 缺陷改变了变性特征.
  • 组合类型 (热与力) 影响DNA缺陷的表现.
关键词:
在DNA变质过程中,DNA变质缺陷的缺陷 缺陷的缺陷这是一个PBD模型.

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Proofreading and DNA Repair Assay Using Single Nucleotide Extension and MALDI-TOF Mass Spectrometry Analysis
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Last Updated: Jul 28, 2025

Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers
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Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers

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Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers
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Proofreading and DNA Repair Assay Using Single Nucleotide Extension and MALDI-TOF Mass Spectrometry Analysis
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Proofreading and DNA Repair Assay Using Single Nucleotide Extension and MALDI-TOF Mass Spectrometry Analysis

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