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TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs
Abstract 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 seq...
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Published in: | Nucleic acids research 2023-07, Vol.51 (W1), p.W577-W586 |
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creator | Woźniak, Tomasz Sura, Weronika Kazimierska, Marta Kasprzyk, Marta Elżbieta Podralska, Marta Dzikiewicz-Krawczyk, Agnieszka |
description | Abstract
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/.
Graphical Abstract
Graphical Abstract
TransCRISPR searches for specific sequence motifs in the user-provided genomic regions and designs optimal sgRNAs targeting them. Results are shown in downloadable tables and visualizations, summarizing features of identified motifs and designed sgRNAs such as genomic localization, quality scores, closest transcription start sites and others. |
doi_str_mv | 10.1093/nar/gkad355 |
format | article |
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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/.
Graphical Abstract
Graphical Abstract
TransCRISPR searches for specific sequence motifs in the user-provided genomic regions and designs optimal sgRNAs targeting them. Results are shown in downloadable tables and visualizations, summarizing features of identified motifs and designed sgRNAs such as genomic localization, quality scores, closest transcription start sites and others.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkad355</identifier><identifier>PMID: 37158253</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Binding Sites - genetics ; CRISPR-Cas Systems - genetics ; Genome ; Genomics - instrumentation ; Genomics - methods ; Internet ; Molecular Conformation ; RNA, Guide, CRISPR-Cas Systems ; Web Server Issue</subject><ispartof>Nucleic acids research, 2023-07, Vol.51 (W1), p.W577-W586</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. 2023</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c371t-7cebaab9793560b8204343b4a0af7f8df960c24931e8512f36b2c25a76c43a523</cites><orcidid>0000-0003-2066-2581 ; 0000-0002-7387-8194 ; 0000-0003-0304-3615 ; 0000-0001-9720-7881 ; 0000-0003-1286-7261 ; 0000-0001-7633-2114</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320084/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320084/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1604,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37158253$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Woźniak, Tomasz</creatorcontrib><creatorcontrib>Sura, Weronika</creatorcontrib><creatorcontrib>Kazimierska, Marta</creatorcontrib><creatorcontrib>Kasprzyk, Marta Elżbieta</creatorcontrib><creatorcontrib>Podralska, Marta</creatorcontrib><creatorcontrib>Dzikiewicz-Krawczyk, Agnieszka</creatorcontrib><title>TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>Abstract
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/.
Graphical Abstract
Graphical Abstract
TransCRISPR searches for specific sequence motifs in the user-provided genomic regions and designs optimal sgRNAs targeting them. Results are shown in downloadable tables and visualizations, summarizing features of identified motifs and designed sgRNAs such as genomic localization, quality scores, closest transcription start sites and others.</description><subject>Binding Sites - genetics</subject><subject>CRISPR-Cas Systems - genetics</subject><subject>Genome</subject><subject>Genomics - instrumentation</subject><subject>Genomics - methods</subject><subject>Internet</subject><subject>Molecular Conformation</subject><subject>RNA, Guide, CRISPR-Cas Systems</subject><subject>Web Server Issue</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kctOGzEUhq2KqgTaFXvkFUJC0xzf5rJCUQQlEoIqTbe1PI49GCbjwZ5UdNd36Bv2STBKQLBhdRbn03f-ox-hAwJfCVRs3Kkwbu7UkgnxAY0Iy2nGq5zuoBEwEBkBXu6ivRhvAQgngn9Cu6wgoqSCjdCvRVBdnM5nP77P___9F5v51QQvTXRNhwfvW2x9wJv1eKpihc1Db4JbmW6IeFChMYPrGhx7o511GkdzvzadNnjlB2fjZ_TRqjaaL9u5j36eny2mF9nl9bfZdHKZ6RRlyAptaqXqqqiYyKEuKXDGWc0VKFvYcmmrHDTlFSOmFIRaltdUU6GKXHOmBGX76HTj7df1yix1ihdUK_uUVIU_0isn3246dyMb_1sSYBSg5MlwvDUEn16Ig1y5qE3bqs74dZS0JEQUwAUk9GSD6uBjDMa-3CEgnyqRqRK5rSTRh6-jvbDPHSTgaAP4df-u6RG2dpbj</recordid><startdate>20230705</startdate><enddate>20230705</enddate><creator>Woźniak, Tomasz</creator><creator>Sura, Weronika</creator><creator>Kazimierska, Marta</creator><creator>Kasprzyk, Marta Elżbieta</creator><creator>Podralska, Marta</creator><creator>Dzikiewicz-Krawczyk, Agnieszka</creator><general>Oxford University Press</general><scope>TOX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2066-2581</orcidid><orcidid>https://orcid.org/0000-0002-7387-8194</orcidid><orcidid>https://orcid.org/0000-0003-0304-3615</orcidid><orcidid>https://orcid.org/0000-0001-9720-7881</orcidid><orcidid>https://orcid.org/0000-0003-1286-7261</orcidid><orcidid>https://orcid.org/0000-0001-7633-2114</orcidid></search><sort><creationdate>20230705</creationdate><title>TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs</title><author>Woźniak, Tomasz ; Sura, Weronika ; Kazimierska, Marta ; Kasprzyk, Marta Elżbieta ; Podralska, Marta ; Dzikiewicz-Krawczyk, Agnieszka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-7cebaab9793560b8204343b4a0af7f8df960c24931e8512f36b2c25a76c43a523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Binding Sites - genetics</topic><topic>CRISPR-Cas Systems - genetics</topic><topic>Genome</topic><topic>Genomics - instrumentation</topic><topic>Genomics - methods</topic><topic>Internet</topic><topic>Molecular Conformation</topic><topic>RNA, Guide, CRISPR-Cas Systems</topic><topic>Web Server Issue</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woźniak, Tomasz</creatorcontrib><creatorcontrib>Sura, Weronika</creatorcontrib><creatorcontrib>Kazimierska, Marta</creatorcontrib><creatorcontrib>Kasprzyk, Marta Elżbieta</creatorcontrib><creatorcontrib>Podralska, Marta</creatorcontrib><creatorcontrib>Dzikiewicz-Krawczyk, Agnieszka</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woźniak, Tomasz</au><au>Sura, Weronika</au><au>Kazimierska, Marta</au><au>Kasprzyk, Marta Elżbieta</au><au>Podralska, Marta</au><au>Dzikiewicz-Krawczyk, Agnieszka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2023-07-05</date><risdate>2023</risdate><volume>51</volume><issue>W1</issue><spage>W577</spage><epage>W586</epage><pages>W577-W586</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>Abstract
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/.
Graphical Abstract
Graphical Abstract
TransCRISPR searches for specific sequence motifs in the user-provided genomic regions and designs optimal sgRNAs targeting them. Results are shown in downloadable tables and visualizations, summarizing features of identified motifs and designed sgRNAs such as genomic localization, quality scores, closest transcription start sites and others.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>37158253</pmid><doi>10.1093/nar/gkad355</doi><orcidid>https://orcid.org/0000-0003-2066-2581</orcidid><orcidid>https://orcid.org/0000-0002-7387-8194</orcidid><orcidid>https://orcid.org/0000-0003-0304-3615</orcidid><orcidid>https://orcid.org/0000-0001-9720-7881</orcidid><orcidid>https://orcid.org/0000-0003-1286-7261</orcidid><orcidid>https://orcid.org/0000-0001-7633-2114</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Binding Sites - genetics CRISPR-Cas Systems - genetics Genome Genomics - instrumentation Genomics - methods Internet Molecular Conformation RNA, Guide, CRISPR-Cas Systems Web Server Issue |
title | TransCRISPR–sgRNA design tool for CRISPR/Cas9 experiments targeting specific sequence motifs |
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