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Related Concept Videos

What is Genetic Engineering?00:49

What is Genetic Engineering?

Overview
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...
Gene Conversion02:08

Gene Conversion

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...
CRISPR01:59

CRISPR

Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced Short...
In-vitro Mutagenesis01:16

In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
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...

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Updated: Jul 10, 2026

Genome Editing in Mammalian Cell Lines using CRISPR-Cas
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Genome Editing in Mammalian Cell Lines using CRISPR-Cas

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Chromosomal engineering.

Alistair Duncan1, Gyula Hadlaczky

  • 1Chromos Molecular Systems Inc., 8081 Lougheed Highway, Burnaby, BC, Canada V5A 1W9.

Current Opinion in Biotechnology
|November 6, 2007
PubMed
Summary

Artificial chromosomes (ACs) are stable, large-capacity vectors for gene technology. These engineered chromosomes offer potential for protein manufacturing, animal production, and gene therapy applications.

Area of Science:

  • Biotechnology
  • Molecular Biology
  • Genetics Engineering

Background:

  • Artificial chromosomes (ACs) are engineered DNA molecules.
  • ACs function as non-integrating vectors with high stability and carrying capacity.
  • They enable the inclusion of multiple transgenes and regulatory elements.

Purpose of the Study:

  • To highlight the capabilities of artificial chromosome-based systems.
  • To discuss their potential applications in gene technology.
  • To identify future research directions.

Main Methods:

  • Engineering of ACs to harbor and express genes of interest.
  • Utilizing recombination systems for custom AC construction.
  • Reviewing recent advances in AC technologies.

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Site-specific Bacterial Chromosome Engineering: ΦC31 Integrase Mediated Cassette Exchange (IMCE)
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Site-specific Bacterial Chromosome Engineering: ΦC31 Integrase Mediated Cassette Exchange (IMCE)

Published on: March 16, 2012

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Last Updated: Jul 10, 2026

Genome Editing in Mammalian Cell Lines using CRISPR-Cas
07:56

Genome Editing in Mammalian Cell Lines using CRISPR-Cas

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Subcloning Plus Insertion (SPI) - A Novel Recombineering Method for the Rapid Construction of Gene Targeting Vectors
09:02

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

Published on: January 8, 2015

Site-specific Bacterial Chromosome Engineering: ΦC31 Integrase Mediated Cassette Exchange (IMCE)
08:21

Site-specific Bacterial Chromosome Engineering: ΦC31 Integrase Mediated Cassette Exchange (IMCE)

Published on: March 16, 2012

Main Results:

  • ACs provide large carrying capacity for complex genetic constructs.
  • They allow for regulated transgene expression.
  • AC systems are versatile tools for various applications.

Conclusions:

  • Artificial chromosomes represent a powerful platform for gene technology.
  • Further research is needed to overcome current limitations.
  • ACs hold significant promise for cellular protein production, transgenic animal development, and gene therapy.