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CRISPR Cpf1 proteins: structure, function and implications for genome editing
CRISPR and CRISPR-associated (Cas) protein, as components of microbial adaptive immune system, allows biologists to edit genomic DNA in a precise and specific way. CRISPR-Cas systems are classified into two main classes and six types. Cpf1 is a putative type V (class II) CRISPR effector, which can b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507119/ https://www.ncbi.nlm.nih.gov/pubmed/31086658 http://dx.doi.org/10.1186/s13578-019-0298-7 |
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author | Safari, Fatemeh Zare, Khadijeh Negahdaripour, Manica Barekati-Mowahed, Mazyar Ghasemi, Younes |
author_facet | Safari, Fatemeh Zare, Khadijeh Negahdaripour, Manica Barekati-Mowahed, Mazyar Ghasemi, Younes |
author_sort | Safari, Fatemeh |
collection | PubMed |
description | CRISPR and CRISPR-associated (Cas) protein, as components of microbial adaptive immune system, allows biologists to edit genomic DNA in a precise and specific way. CRISPR-Cas systems are classified into two main classes and six types. Cpf1 is a putative type V (class II) CRISPR effector, which can be programmed with a CRISPR RNA to bind and cleave complementary DNA targets. Cpf1 has recently emerged as an alternative for Cas9, due to its distinct features such as the ability to target T-rich motifs, no need for trans-activating crRNA, inducing a staggered double-strand break and potential for both RNA processing and DNA nuclease activity. In this review, we attempt to discuss the evolutionary origins, basic architectures, and molecular mechanisms of Cpf1 family proteins, as well as crRNA designing and delivery strategies. We will also describe the novel Cpf1 variants, which have broadened the versatility and feasibility of this system in genome editing, transcription regulation, epigenetic modulation, and base editing. Finally, we will be reviewing the recent studies on utilization of Cpf1as a molecular tool for genome editing. |
format | Online Article Text |
id | pubmed-6507119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65071192019-05-13 CRISPR Cpf1 proteins: structure, function and implications for genome editing Safari, Fatemeh Zare, Khadijeh Negahdaripour, Manica Barekati-Mowahed, Mazyar Ghasemi, Younes Cell Biosci Review CRISPR and CRISPR-associated (Cas) protein, as components of microbial adaptive immune system, allows biologists to edit genomic DNA in a precise and specific way. CRISPR-Cas systems are classified into two main classes and six types. Cpf1 is a putative type V (class II) CRISPR effector, which can be programmed with a CRISPR RNA to bind and cleave complementary DNA targets. Cpf1 has recently emerged as an alternative for Cas9, due to its distinct features such as the ability to target T-rich motifs, no need for trans-activating crRNA, inducing a staggered double-strand break and potential for both RNA processing and DNA nuclease activity. In this review, we attempt to discuss the evolutionary origins, basic architectures, and molecular mechanisms of Cpf1 family proteins, as well as crRNA designing and delivery strategies. We will also describe the novel Cpf1 variants, which have broadened the versatility and feasibility of this system in genome editing, transcription regulation, epigenetic modulation, and base editing. Finally, we will be reviewing the recent studies on utilization of Cpf1as a molecular tool for genome editing. BioMed Central 2019-05-09 /pmc/articles/PMC6507119/ /pubmed/31086658 http://dx.doi.org/10.1186/s13578-019-0298-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Safari, Fatemeh Zare, Khadijeh Negahdaripour, Manica Barekati-Mowahed, Mazyar Ghasemi, Younes CRISPR Cpf1 proteins: structure, function and implications for genome editing |
title | CRISPR Cpf1 proteins: structure, function and implications for genome editing |
title_full | CRISPR Cpf1 proteins: structure, function and implications for genome editing |
title_fullStr | CRISPR Cpf1 proteins: structure, function and implications for genome editing |
title_full_unstemmed | CRISPR Cpf1 proteins: structure, function and implications for genome editing |
title_short | CRISPR Cpf1 proteins: structure, function and implications for genome editing |
title_sort | crispr cpf1 proteins: structure, function and implications for genome editing |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507119/ https://www.ncbi.nlm.nih.gov/pubmed/31086658 http://dx.doi.org/10.1186/s13578-019-0298-7 |
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