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Related Concept Videos

CRISPR01:59

CRISPR

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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/Cas9 Genome Editing01:28

CRISPR/Cas9 Genome Editing

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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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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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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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Related Experiment Video

Updated: Jul 13, 2025

CRISPR Epigenome Editing in Human Cells using Plasmid DNA Transfection and mRNA Nucleofection Delivery
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CRISPR Epigenome Editing in Human Cells using Plasmid DNA Transfection and mRNA Nucleofection Delivery

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Digital data storage on DNA tape using CRISPR base editors.

Afsaneh Sadremomtaz1, Robert F Glass2, Jorge Eduardo Guerrero1

  • 1Department of Nanoengineering, Joint School of Nanoscience and Nanoengineering, NC A&T State University, Greensboro, NC, USA.

Nature Communications
|October 13, 2023
PubMed
Summary
This summary is machine-generated.

Researchers developed DNA Mutational Overwriting Storage (DMOS), a novel method for digital data storage. This environmentally friendly approach uses CRISPR base editing to write information onto DNA tapes, overcoming limitations of current digital memory technologies.

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Area of Science:

  • Biotechnology
  • Molecular Engineering
  • Data Storage

Background:

  • Archival digital memory faces physical limitations with increasing data demands.
  • DNA offers superior durability, capacity, and energy efficiency for data storage.
  • Existing DNA data storage methods often rely on non-scalable, waste-producing synthesis techniques.

Purpose of the Study:

  • To develop an industrially scalable and environmentally friendly DNA-based digital data storage system.
  • To leverage CRISPR base editing for efficient and targeted information writing on DNA.
  • To demonstrate a proof of concept for the DNA Mutational Overwriting Storage (DMOS) system.

Main Methods:

  • Utilized combinatorial, addressable, orthogonal, and independent in vitro CRISPR base-editing reactions.
  • Developed a system inspired by semiconductor memory architecture and gene editing advancements.
  • Wrote data onto a pool of greenly synthesized DNA tapes.

Main Results:

  • Successfully demonstrated writing and accurate reading of digital data on DNA tapes.
  • Stored a bitmap image of a school logo and the study's title as proof of concept.
  • Validated the feasibility of the DMOS system for molecular digital data storage.

Conclusions:

  • The DMOS system presents a viable, eco-friendly alternative for digital data storage.
  • CRISPR base editing enables efficient and addressable data writing on DNA.
  • This technology addresses the limitations of current digital memory and unsustainable DNA synthesis methods.