Your browser doesn't support javascript.
loading
Meet the Anti-CRISPRs: Widespread Protein Inhibitors of CRISPR-Cas Systems.
Hwang, Sungwon; Maxwell, Karen L.
Afiliação
  • Hwang S; Department of Biochemistry, University of Toronto, Toronto, Canada.
  • Maxwell KL; Department of Biochemistry, University of Toronto, Toronto, Canada.
CRISPR J ; 2(1): 23-30, 2019 02.
Article em En | MEDLINE | ID: mdl-31021234
ABSTRACT
The constant selective pressure exerted by phages, the viruses that infect bacteria, has led to the evolution of a wide range of anti-phage defenses. One of these defense mechanisms, CRISPR-Cas, provides an adaptive immune system to battle phage infection and inhibit horizontal gene transfer by plasmids, transposons, and other mobile genetic elements. Although CRISPR-Cas systems are widespread in bacteria and archaea, they appear to have minimal long-term evolutionary effects with respect to limiting horizontal gene transfer. One factor that may contribute to this may be the presence of potent inhibitors of CRISPR-Cas systems, known as anti-CRISPR proteins. Forty unique families of anti-CRISPR proteins have been described to date. These inhibitors, which are active against both Class 1 and 2 CRISPR-Cas systems, have a wide range of mechanisms of activity. Studies of these proteins have provided important insight into the evolutionary arms race between bacteria and phages, and have contributed to the development of biotechnological tools that can be harnessed for control of CRISPR-Cas genome editing.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Bacteriófagos / Proteínas Virais / Genoma Viral / Archaea / Fagos de Pseudomonas / Sistemas CRISPR-Cas Idioma: En Revista: CRISPR J Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Bacteriófagos / Proteínas Virais / Genoma Viral / Archaea / Fagos de Pseudomonas / Sistemas CRISPR-Cas Idioma: En Revista: CRISPR J Ano de publicação: 2019 Tipo de documento: Article