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Related Concept Videos

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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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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RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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The present-day mitochondrial and chloroplast genomes have retained some of the characteristics of their ancestral prokaryotes and also have acquired new attributes during their evolution within eukaryotic cells. Like prokaryotic genomes, mitochondrial and chloroplast genomes neither bind with histone-like proteins nor show complex packaging into chromosome-like structures, as observed in eukaryotes. Unlike mitotic cell divisions observed in eukaryotic cells, mitochondria and chloroplasts...
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CRISPR/Cas9 Ribonucleoprotein-mediated Precise Gene Editing by Tube Electroporation
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CRISPR-Cas9; an efficient tool for precise plant genome editing.

Waqar Islam1

  • 1College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, Fuzhou, 350002, China; Govt.of Punjab, Agriculture Department, Lahore, Pakistan.

Molecular and Cellular Probes
|April 6, 2018
PubMed
Summary

CRISPR-Cas9 technology enables efficient plant genome editing by inducing DNA breaks for repair. This review summarizes CRISPR applications in plants, highlighting stable mutation generation and alternative DNA editing strategies.

Keywords:
DNAGenetic engineeringGenetic mutationHomologous recombinationTranscription

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Area of Science:

  • Plant Biotechnology
  • Molecular Biology
  • Genetics

Background:

  • Efficient plant genome editing relies on inducing targeted double-stranded DNA breaks (DSBs).
  • DNA repair mechanisms, including homologous recombination (HR) and non-homologous end joining (NHEJ), follow DSB induction.
  • CRISPR-Cas9 has emerged as a transformative tool for genetic manipulation due to its versatility and ease of use.

Purpose of the Study:

  • To review the applications of CRISPR-Cas9 technology in plant genome editing.
  • To discuss the successful adaptation of CRISPR in various plant species for generating stable mutations.
  • To explore alternative genome editing approaches for minimizing off-target effects.

Main Methods:

  • Review of existing literature on CRISPR-Cas9 in plant genome editing.
  • Analysis of successful CRISPR-Cas9 adaptations across different plant species.
  • Examination of strategies employing single DNA lesion induction (e.g., deletions, nickases).

Main Results:

  • CRISPR-Cas9 has been successfully adapted for genome editing in numerous plant species.
  • The NHEJ pathway is frequently utilized for generating stable mutations via CRISPR-Cas9.
  • Alternative methods like genomic deletion and paired nickases offer ways to reduce off-target mutations.

Conclusions:

  • CRISPR-Cas9 is a powerful and adaptable tool for plant genome editing, enabling efficient mutation generation.
  • The application of CRISPR-Cas9 is expanding across a growing number of plant species.
  • Further research into alternative strategies can enhance the precision and safety of plant genome editing.