Cargando…
TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs
Eukaryotic genomes contain several types of recurrent sequence motifs, e.g. transcription factor motifs, miRNA binding sites, repetitive elements. CRISPR/Cas9 can facilitate identification and study of crucial motifs. We present transCRISPR, the first online tool dedicated to search for sequence mot...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320084/ https://www.ncbi.nlm.nih.gov/pubmed/37158253 http://dx.doi.org/10.1093/nar/gkad355 |
_version_ | 1785068373896331264 |
---|---|
author | Woźniak, Tomasz Sura, Weronika Kazimierska, Marta Kasprzyk, Marta Elżbieta Podralska, Marta Dzikiewicz-Krawczyk, Agnieszka |
author_facet | Woźniak, Tomasz Sura, Weronika Kazimierska, Marta Kasprzyk, Marta Elżbieta Podralska, Marta Dzikiewicz-Krawczyk, Agnieszka |
author_sort | Woźniak, Tomasz |
collection | PubMed |
description | Eukaryotic genomes contain several types of recurrent sequence motifs, e.g. transcription factor motifs, miRNA binding sites, repetitive elements. CRISPR/Cas9 can facilitate identification and study of crucial motifs. We present transCRISPR, the first online tool dedicated to search for sequence motifs in the user-provided genomic regions and design optimal sgRNAs targeting them. Users can obtain sgRNAs for chosen motifs, for up to tens of thousands of target regions in 30 genomes, either for the Cas9 or dCas9 system. TransCRISPR provides user-friendly tables and visualizations, summarizing features of identified motifs and designed sgRNAs such as genomic localization, quality scores, closest transcription start sites and others. Experimental validation of sgRNAs for MYC binding sites designed with transCRISPR confirmed efficient disruption of the targeted motifs and effect on expression of MYC-regulated genes. TransCRISPR is available from https://transcrispr.igcz.poznan.pl/transcrispr/. |
format | Online Article Text |
id | pubmed-10320084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103200842023-07-06 TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs Woźniak, Tomasz Sura, Weronika Kazimierska, Marta Kasprzyk, Marta Elżbieta Podralska, Marta Dzikiewicz-Krawczyk, Agnieszka Nucleic Acids Res Web Server Issue Eukaryotic genomes contain several types of recurrent sequence motifs, e.g. transcription factor motifs, miRNA binding sites, repetitive elements. CRISPR/Cas9 can facilitate identification and study of crucial motifs. We present transCRISPR, the first online tool dedicated to search for sequence motifs in the user-provided genomic regions and design optimal sgRNAs targeting them. Users can obtain sgRNAs for chosen motifs, for up to tens of thousands of target regions in 30 genomes, either for the Cas9 or dCas9 system. TransCRISPR provides user-friendly tables and visualizations, summarizing features of identified motifs and designed sgRNAs such as genomic localization, quality scores, closest transcription start sites and others. Experimental validation of sgRNAs for MYC binding sites designed with transCRISPR confirmed efficient disruption of the targeted motifs and effect on expression of MYC-regulated genes. TransCRISPR is available from https://transcrispr.igcz.poznan.pl/transcrispr/. Oxford University Press 2023-05-09 /pmc/articles/PMC10320084/ /pubmed/37158253 http://dx.doi.org/10.1093/nar/gkad355 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Web Server Issue Woźniak, Tomasz Sura, Weronika Kazimierska, Marta Kasprzyk, Marta Elżbieta Podralska, Marta Dzikiewicz-Krawczyk, Agnieszka TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs |
title | TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs |
title_full | TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs |
title_fullStr | TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs |
title_full_unstemmed | TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs |
title_short | TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs |
title_sort | transcrispr–sgrna design tool for crispr/cas9 experiments targeting specific sequence motifs |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320084/ https://www.ncbi.nlm.nih.gov/pubmed/37158253 http://dx.doi.org/10.1093/nar/gkad355 |
work_keys_str_mv | AT wozniaktomasz transcrisprsgrnadesigntoolforcrisprcas9experimentstargetingspecificsequencemotifs AT suraweronika transcrisprsgrnadesigntoolforcrisprcas9experimentstargetingspecificsequencemotifs AT kazimierskamarta transcrisprsgrnadesigntoolforcrisprcas9experimentstargetingspecificsequencemotifs AT kasprzykmartaelzbieta transcrisprsgrnadesigntoolforcrisprcas9experimentstargetingspecificsequencemotifs AT podralskamarta transcrisprsgrnadesigntoolforcrisprcas9experimentstargetingspecificsequencemotifs AT dzikiewiczkrawczykagnieszka transcrisprsgrnadesigntoolforcrisprcas9experimentstargetingspecificsequencemotifs |