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Related Concept Videos

CRISPR/Cas9 Genome Editing01:28

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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...
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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...
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CRISPR and crRNAs02:53

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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.
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A New Toolkit for Evaluating Gene Functions using Conditional Cas9 Stabilization
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Regulating CRISPR/Cas9 Function through Conditional Guide RNA Control.

Wes Brown1, Wenyuan Zhou1, Alexander Deiters1

  • 1Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, PA 15260, USA.

Chembiochem : a European Journal of Chemical Biology
|August 25, 2020
PubMed
Summary
This summary is machine-generated.

New CRISPR/Cas9 gene editing methods use modified guide RNAs (gRNAs) for precise control. These strategies, including light or small molecule activation, offer advantages over protein-based approaches for regulating gene editing and transcription.

Keywords:
CRISPRCas9gene editingnucleic acidoptical controlprotection groups

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Area of Science:

  • Molecular Biology
  • Gene Editing Technologies
  • Biotechnology

Background:

  • CRISPR/Cas9 gene editing offers powerful tools for genetic manipulation.
  • Previous control strategies primarily focused on modifying the Cas9 enzyme.
  • A need exists for alternative, precise methods to regulate CRISPR/Cas9 activity.

Purpose of the Study:

  • To review and discuss recent strategies for conditional control of CRISPR/Cas9.
  • To focus on modifications of the guide RNA (gRNA) for conditional function.
  • To compare the effectiveness of different gRNA-based control methods.

Main Methods:

  • Discussion of gRNA modifications for conditional CRISPR/Cas9 control.
  • Analysis of methods involving light, small molecules, proteins, and oligonucleotides.
  • Comparative evaluation of the advantages and effectiveness of these strategies.

Main Results:

  • Guide RNA (gRNA) modifications provide effective conditional control of CRISPR/Cas9.
  • Methods include gRNA control by light, small molecules, proteins, and oligonucleotides.
  • These gRNA-based approaches offer precise regulation of gene editing and transcription.

Conclusions:

  • Guide RNA modifications represent a promising avenue for conditional CRISPR/Cas9 control.
  • These strategies offer distinct advantages over traditional Cas9-centric approaches.
  • Further research into gRNA-based methods can enhance precision in gene editing applications.