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Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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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...
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Homologous Recombination02:31

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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 Replisome03:01

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DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
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The Replisome03:01

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Mismatch Repair01:20

Mismatch Repair

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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...
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Related Experiment Video

Updated: Apr 8, 2026

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

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The Serine Recombinases.

W Marshall Stark1

  • 1Institute of Molecular, Cell and Systems Biology, University of Glasgow, Bower Building, Glasgow G12 8QQ, Scotland, United Kingdom.

Microbiology Spectrum
|June 25, 2015
PubMed
Summary

This chapter explores serine recombinases, enzymes crucial for DNA manipulation. It details their types, biological roles, structures, catalytic mechanisms, regulation, and diverse applications in biotechnology.

Area of Science:

  • Molecular Biology
  • Enzymology
  • Genetics

Background:

  • Site-specific recombination is a fundamental DNA process involving recognition, cutting, and rejoining of specific DNA sequences by enzymes called recombinases.
  • Recombinases are classified into two main families: tyrosine and serine recombinases, distinguished by their conserved catalytic amino acid residue.

Purpose of the Study:

  • To provide a comprehensive overview of serine recombinases.
  • To elucidate their diverse biological roles, structural characteristics, and catalytic mechanisms.
  • To discuss regulatory mechanisms and potential applications of serine recombinases.

Main Methods:

  • Review of existing literature on serine recombinase research.
  • Analysis of protein sequences and structural data to understand mechanisms.

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Subcloning Plus Insertion SPI - A Novel Recombineering Method for the Rapid Construction of Gene Targeting Vectors

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Related Experiment Videos

Last Updated: Apr 8, 2026

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

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Principles of Site-Specific Recombinase SSR Technology
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Principles of Site-Specific Recombinase SSR Technology

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Subcloning Plus Insertion SPI - A Novel Recombineering Method for the Rapid Construction of Gene Targeting Vectors
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  • Examination of biological contexts and experimental applications.
  • Main Results:

    • Detailed classification of serine recombinases based on sequence and mechanism.
    • Explanation of the conserved serine residue's role in DNA cleavage and strand transfer.
    • Identification of various biological functions and biotechnological uses.

    Conclusions:

    • Serine recombinases are a vital class of enzymes with complex mechanisms and broad applicability.
    • Understanding their intricacies facilitates advancements in genetic engineering and synthetic biology.
    • Further research promises expanded applications in gene editing and therapeutic strategies.