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Anti-CRISPRs: Protein Inhibitors of CRISPR-Cas Systems
- Source :
- Annu Rev Biochem
- Publication Year :
- 2020
- Publisher :
- Annual Reviews, 2020.
-
Abstract
- Clustered regularly interspaced short palindromic repeats (CRISPR) together with their accompanying cas (CRISPR-associated) genes are found frequently in bacteria and archaea, serving to defend against invading foreign DNA, such as viral genomes. CRISPR-Cas systems provide a uniquely powerful defense because they can adapt to newly encountered genomes. The adaptive ability of these systems has been exploited, leading to their development as highly effective tools for genome editing. The widespread use of CRISPR-Cas systems has driven a need for methods to control their activity. This review focuses on anti-CRISPRs (Acrs), proteins produced by viruses and other mobile genetic elements that can potently inhibit CRISPR-Cas systems. Discovered in 2013, there are now 54 distinct families of these proteins described, and the functional mechanisms of more than a dozen have been characterized in molecular detail. The investigation of Acrs is leading to a variety of practical applications and is providing exciting new insight into the biology of CRISPR-Cas systems.
- Subjects :
- Models, Molecular
CRISPR-Associated Proteins
Computational biology
Biology
Biochemistry
Genome
Article
Biological Coevolution
Small Molecule Libraries
Bacteriophage
Viral Proteins
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Bacterial Proteins
Genome editing
Humans
CRISPR
DNA Cleavage
Gene
030304 developmental biology
Gene Editing
0303 health sciences
Endodeoxyribonucleases
Bacteria
Palindrome
DNA
biology.organism_classification
Archaea
chemistry
Multigene Family
Viruses
CRISPR-Cas Systems
Protein Multimerization
Mobile genetic elements
030217 neurology & neurosurgery
Protein Binding
RNA, Guide, Kinetoplastida
Subjects
Details
- ISSN :
- 15454509 and 00664154
- Volume :
- 89
- Database :
- OpenAIRE
- Journal :
- Annual Review of Biochemistry
- Accession number :
- edsair.doi.dedup.....74433db15cb7b390d0ab9a3df3cdb8af
- Full Text :
- https://doi.org/10.1146/annurev-biochem-011420-111224