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Chemistry of Class 1 CRISPR-Cas effectors: Binding, editing, and regulation.
Liu, Tina Y; Doudna, Jennifer A.
Afiliação
  • Liu TY; Department of Molecular and Cell Biology, University of California, Berkeley, California, USA.
  • Doudna JA; Department of Molecular and Cell Biology, University of California, Berkeley, California, USA doudna@berkeley.edu.
J Biol Chem ; 295(42): 14473-14487, 2020 10 16.
Article em En | MEDLINE | ID: mdl-32817336
ABSTRACT
Among the multiple antiviral defense mechanisms found in prokaryotes, CRISPR-Cas systems stand out as the only known RNA-programmed pathways for detecting and destroying bacteriophages and plasmids. Class 1 CRISPR-Cas systems, the most widespread and diverse of these adaptive immune systems, use an RNA-guided multiprotein complex to find foreign nucleic acids and trigger their destruction. In this review, we describe how these multisubunit complexes target and cleave DNA and RNA and how regulatory molecules control their activities. We also highlight similarities to and differences from Class 2 CRISPR-Cas systems, which use a single-protein effector, as well as other types of bacterial and eukaryotic immune systems. We summarize current applications of the Class 1 CRISPR-Cas systems for DNA/RNA modification, control of gene expression, and nucleic acid detection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistemas CRISPR-Cas / Edição de Genes Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistemas CRISPR-Cas / Edição de Genes Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article