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The discovery and development of the CRISPR system in applications in genome manipulation.
- Source :
-
Biochemistry and cell biology = Biochimie et biologie cellulaire [Biochem Cell Biol] 2017 Apr; Vol. 95 (2), pp. 203-210. Date of Electronic Publication: 2016 Oct 28. - Publication Year :
- 2017
-
Abstract
- The clustered regularly interspaced short palindromic repeat (CRISPR) associated 9 (Cas9) system is a microbial adaptive immune system that has been recently developed for genomic engineering. From the moment the CRISPR system was discovered in Escherichia coli, the drive to understand the mechanism prevailed, leading to rapid advancement in the knowledge and applications of the CRISPR system. With the ability to characterize and understand the function of the Cas9 endonuclease came the ability to adapt the CRISPR-Cas9 system for use in a variety of applications and disciplines ranging from agriculture to biomedicine. This review will provide a brief overview of the discovery and development of the CRISPR-Cas9 system in applications such as genome regulation and epigenome engineering, as well as the challenges faced.
- Subjects :
- Animals
Bacterial Proteins metabolism
Breeding
CRISPR-Associated Protein 9
Cattle
Chickens
Endonucleases metabolism
Escherichia coli genetics
Escherichia coli immunology
Gene Editing ethics
Gene Editing history
Gene Expression
Genetic Engineering ethics
Genetic Engineering history
History, 20th Century
History, 21st Century
Humans
RNA, Guide, CRISPR-Cas Systems genetics
RNA, Guide, CRISPR-Cas Systems metabolism
Bacterial Proteins genetics
CRISPR-Cas Systems
Clustered Regularly Interspaced Short Palindromic Repeats
Endonucleases genetics
Gene Editing methods
Genetic Engineering methods
Genome
Subjects
Details
- Language :
- English
- ISSN :
- 1208-6002
- Volume :
- 95
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Biochemistry and cell biology = Biochimie et biologie cellulaire
- Publication Type :
- Academic Journal
- Accession number :
- 28103055
- Full Text :
- https://doi.org/10.1139/bcb-2016-0159