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相关概念视频

Translesion DNA Polymerases02:10

Translesion DNA Polymerases

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...
Homologous Recombination02:31

Homologous Recombination

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...
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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, a...
Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
Crossing Over01:30

Crossing Over

Crossing over is the exchange of genetic information between homologous chromosomes during prophase I of meiosis I. Genetic recombination gives rise to allelic diversity in the newly formed daughter cells. In humans, crossing over produces genetically distinct haploid egg and sperm cells that undergo fertilization to produce unique offspring. Before cell division starts, the germ cell’s chromosome(s) undergo duplication in the S phase of the cell cycle. As the cells enter prophase I, duplicated...

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相关实验视频

Updated: Jul 19, 2026

Quantitation and Analysis of the Formation of HO-Endonuclease Stimulated Chromosomal Translocations by Single-Strand Annealing in Saccharomyces cerevisiae
09:40

Quantitation and Analysis of the Formation of HO-Endonuclease Stimulated Chromosomal Translocations by Single-Strand Annealing in Saccharomyces cerevisiae

Published on: September 23, 2011

与自杀基质被困的特定地点重组中间体.

S E Nunes-Düby, L Matsumoto, A Landy

    Cell
    |August 28, 1987
    PubMed
    概括

    新的"自杀基质"揭示了兰巴地位特定重组通过连续的单链交换发生,而不是协同切割. 这个顺序取决于蛋白质的排列,Integrase可以执行非互惠的链转移.

    科学领域:

    • 分子生物学分子生物学
    • 遗传学 是一个遗传学.
    • 生物化学 生物化学

    背景情况:

    • 特定位点的重组是关键的DNA操纵过程.
    • 了解兰巴特位特定重组的机制是控制遗传信息的关键.
    • 之前的模型提出了协同切割DNA链的方案,但缺乏明确的证据.

    研究的目的:

    • 为了阐明Lambda位点特定重组的精确机制.
    • 为了研究蛋白质排列在重组顺序中的作用.
    • 为了确定Integrase蛋白质的链转移能力.

    主要方法:

    • 设计和利用具有战略意义的新型"自杀基材".
    • 分析累积的反应中间体.
    • 整合酶蛋白的链转移活性的表征.

    主要成果:

    • 兰巴达特定位点重组通过两个连续的单链交换进行.
    • 一个协调的四丝切割模型被最终排除在外.
    • 线程交换的顺序在整合和切除中都是不变的.
    • 与交换位点距离的蛋白质排列控制了链交换的顺序.
    • 集成酶蛋白显示出对非互惠的单一DNA链转移的能力.

    更多相关视频

    Preparation of the Mgm101 Recombination Protein by MBP-based Tagging Strategy
    11:40

    Preparation of the Mgm101 Recombination Protein by MBP-based Tagging Strategy

    Published on: June 25, 2013

    Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
    07:55

    Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

    Published on: September 11, 2022

    相关实验视频

    Last Updated: Jul 19, 2026

    Quantitation and Analysis of the Formation of HO-Endonuclease Stimulated Chromosomal Translocations by Single-Strand Annealing in Saccharomyces cerevisiae
    09:40

    Quantitation and Analysis of the Formation of HO-Endonuclease Stimulated Chromosomal Translocations by Single-Strand Annealing in Saccharomyces cerevisiae

    Published on: September 23, 2011

    Preparation of the Mgm101 Recombination Protein by MBP-based Tagging Strategy
    11:40

    Preparation of the Mgm101 Recombination Protein by MBP-based Tagging Strategy

    Published on: June 25, 2013

    Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
    07:55

    Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

    Published on: September 11, 2022

    结论:

    • 兰巴达特定位点重组机制涉及连续的,有序的单链交换.
    • 蛋白质-DNA相互作用决定了重组的方向性.
    • 整合酶具有单向链转移的固有能力.