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Related Concept Videos

CRISPR/Cas9 Genome Editing01:28

CRISPR/Cas9 Genome Editing

The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
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...
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...
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...
CRISPR and crRNAs02:53

CRISPR and crRNAs

Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
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...

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Related Experiment Video

Updated: May 11, 2026

Mouse Genome Engineering Using Designer Nucleases
12:04

Mouse Genome Engineering Using Designer Nucleases

Published on: April 2, 2014

ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering.

Thomas Gaj1, Charles A Gersbach, Carlos F Barbas

  • 1The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA, USA.

Trends in Biotechnology
|May 14, 2013
PubMed
Summary

Zinc-finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs) are powerful gene-editing tools. These nucleases enable precise DNA modifications for research, genetic analysis, and potential therapeutics.

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Area of Science:

  • Molecular Biology
  • Biotechnology
  • Genetics

Background:

  • Zinc-finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs) are engineered DNA-binding proteins fused to nucleases.
  • These chimeric nucleases offer programmable, sequence-specific DNA targeting capabilities.

Purpose of the Study:

  • To review the achievements and applications of ZFN and TALEN technologies in biological research.
  • To discuss the therapeutic potential and future prospects of site-specific nuclease technologies, including CRISPR/Cas systems.

Main Methods:

  • ZFNs and TALENs function by inducing targeted DNA double-strand breaks at specific genomic loci.
  • These breaks are repaired via nonhomologous end joining or homology-directed repair pathways, enabling genetic modifications.

Main Results:

  • ZFNs and TALENs have enabled a wide range of genetic modifications for research and analysis.
  • These technologies demonstrate significant potential for therapeutic applications in treating genetic disorders.

Conclusions:

  • Site-specific nuclease technologies like ZFNs and TALENs are revolutionizing genetic manipulation.
  • The field is rapidly advancing with the emergence of new tools such as CRISPR/Cas systems, promising broader applications.