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Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays
In the past few years, several types of artificial transcriptional activator, based on CRISPR-Cas9, have been developed and refined. Of these, in synergistic activation mediator and SunTag systems, the effector proteins, expressed in trans, can be recruited to the target sites via the MS2 RNA-bindin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636879/ https://www.ncbi.nlm.nih.gov/pubmed/31021277 http://dx.doi.org/10.1089/crispr.2018.0009 |
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author | Kunii, Atsushi Hara, Yoshihiro Takenaga, Mitsumasa Hattori, Naoko Fukazawa, Takuya Ushijima, Toshikazu Yamamoto, Takashi Sakuma, Tetsushi |
author_facet | Kunii, Atsushi Hara, Yoshihiro Takenaga, Mitsumasa Hattori, Naoko Fukazawa, Takuya Ushijima, Toshikazu Yamamoto, Takashi Sakuma, Tetsushi |
author_sort | Kunii, Atsushi |
collection | PubMed |
description | In the past few years, several types of artificial transcriptional activator, based on CRISPR-Cas9, have been developed and refined. Of these, in synergistic activation mediator and SunTag systems, the effector proteins, expressed in trans, can be recruited to the target sites via the MS2 RNA-binding system and GCN4-scFv antibody system, respectively. Here, we report a strong transcriptional activation system achieved by fusing GCN4 repeat to MS2 coat protein to accumulate numbers of activators, fused to scFv antibodies. By targeting the CDH1 gene, we show that our novel system, named “TREE,” results in a greater effect of activating exogenous reporter and endogenous gene. Moreover, by targeting another gene, RANKL, we consistently show the superiority of the TREE system with fewer single-guide RNAs compared to conventional systems. Our TREE system is a promising tool for transcriptional activation and can potentially contribute to other dCas9-mediated technologies such as epigenome editing and chromosome visualization. |
format | Online Article Text |
id | pubmed-6636879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-66368792019-08-20 Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays Kunii, Atsushi Hara, Yoshihiro Takenaga, Mitsumasa Hattori, Naoko Fukazawa, Takuya Ushijima, Toshikazu Yamamoto, Takashi Sakuma, Tetsushi CRISPR J Research Article In the past few years, several types of artificial transcriptional activator, based on CRISPR-Cas9, have been developed and refined. Of these, in synergistic activation mediator and SunTag systems, the effector proteins, expressed in trans, can be recruited to the target sites via the MS2 RNA-binding system and GCN4-scFv antibody system, respectively. Here, we report a strong transcriptional activation system achieved by fusing GCN4 repeat to MS2 coat protein to accumulate numbers of activators, fused to scFv antibodies. By targeting the CDH1 gene, we show that our novel system, named “TREE,” results in a greater effect of activating exogenous reporter and endogenous gene. Moreover, by targeting another gene, RANKL, we consistently show the superiority of the TREE system with fewer single-guide RNAs compared to conventional systems. Our TREE system is a promising tool for transcriptional activation and can potentially contribute to other dCas9-mediated technologies such as epigenome editing and chromosome visualization. Mary Ann Liebert, Inc., publishers 2018-10-01 2018-10-23 /pmc/articles/PMC6636879/ /pubmed/31021277 http://dx.doi.org/10.1089/crispr.2018.0009 Text en © Atsushi Kunii et al. 2018; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kunii, Atsushi Hara, Yoshihiro Takenaga, Mitsumasa Hattori, Naoko Fukazawa, Takuya Ushijima, Toshikazu Yamamoto, Takashi Sakuma, Tetsushi Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays |
title | Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays |
title_full | Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays |
title_fullStr | Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays |
title_full_unstemmed | Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays |
title_short | Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays |
title_sort | three-component repurposed technology for enhanced expression: highly accumulable transcriptional activators via branched tag arrays |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636879/ https://www.ncbi.nlm.nih.gov/pubmed/31021277 http://dx.doi.org/10.1089/crispr.2018.0009 |
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