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相关概念视频

Homologous Recombination02:31

Homologous Recombination

50.9K
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...
50.9K
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

12.8K
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...
12.8K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

10.1K
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...
10.1K
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
LTR Retrotransposons03:08

LTR Retrotransposons

17.8K
LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
17.8K
Gene Conversion02:08

Gene Conversion

9.9K
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
9.9K

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相关实验视频

Updated: Aug 28, 2025

Visualization of DNA Repair Proteins Interaction by Immunofluorescence
07:55

Visualization of DNA Repair Proteins Interaction by Immunofluorescence

Published on: June 26, 2020

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双链断裂修复中的II组内类反转录酶功能

Seung Kuk Park1, Georg Mohr1, Jun Yao1

  • 1Departments of Molecular Biosciences and Oncology, University of Texas at Austin, Austin, TX 78712, USA.

Cell
|September 16, 2022
PubMed
概括

细菌具有用于DNA修复的逆转录酶 (RT). 这些酶通过微同质介导端结合 (MMEJ) 进行转化DNA合成和双链断裂修复 (DSBR).

科学领域:

  • 分子生物学
  • 遗传学
  • 生物化学

背景情况:

  • 细菌编码逆转录酶 (RTs),其结构与II组内核RTs有关,其功能基本未知.
  • 已知II组内RT是参与RNA拼接和回归归的移动遗传元素.

研究的目的:

  • 研究Pseudomonas aeruginosa的II组内体类RT (G2L4RT) 的功能.
  • 确定细菌RT能否在DNA修复途径中发挥作用,特别是转化DNA合成和双链断裂修复 (DSBR).

主要方法:

  • G2L4 RT的生化特征
  • 在大肠杆菌中表达G2L4RT.
  • 位点定向的突变生成以分析活性位点残留物 (YIDD与YADD).
  • 与人类DNA修复聚合酶和其他非LTR反元素RT进行比较分析.

主要成果:

  • 具有YIDD活性位点的G2L4 RT在本地宿主和大肠杆菌中表现出DNA修复活动.
  • G2L4 RT通过微同质介导端结合 (MMEJ) 进行转化DNA合成和DSBR.
  • 它的生物化学活动与人类DNA修复聚合酶甲相似.
  • 在II组内RT和G2L4RT中,相互的活性部位替代显示出异黄素有利于MMEJ,而氨酸有利于原料延伸.
关键词:
另一个DNA 修复聚合酶另一端连接高通量测序昆虫R2元素其他非逆转录酶目标机热稳定的II组内核逆转录酶

更多相关视频

Analysis of DNA Double-strand Break DSB Repair in Mammalian Cells
13:10

Analysis of DNA Double-strand Break DSB Repair in Mammalian Cells

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Characterizing DNA Repair Processes at Transient and Long-lasting Double-strand DNA Breaks by Immunofluorescence Microscopy
08:31

Characterizing DNA Repair Processes at Transient and Long-lasting Double-strand DNA Breaks by Immunofluorescence Microscopy

Published on: June 8, 2018

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相关实验视频

Last Updated: Aug 28, 2025

Visualization of DNA Repair Proteins Interaction by Immunofluorescence
07:55

Visualization of DNA Repair Proteins Interaction by Immunofluorescence

Published on: June 26, 2020

10.3K
Analysis of DNA Double-strand Break DSB Repair in Mammalian Cells
13:10

Analysis of DNA Double-strand Break DSB Repair in Mammalian Cells

Published on: September 8, 2010

31.9K
Characterizing DNA Repair Processes at Transient and Long-lasting Double-strand DNA Breaks by Immunofluorescence Microscopy
08:31

Characterizing DNA Repair Processes at Transient and Long-lasting Double-strand DNA Breaks by Immunofluorescence Microscopy

Published on: June 8, 2018

9.2K

结论:

  • 细菌II组内体类RT具有固有的DNA修复能力,包括DSBR.
  • 这些功能依赖于与真核生物非LTR反元素RT共享的保存结构特征.
  • 细菌RT可能在多种生物体中起着保留作用.