Methods for decoding Cas9 protospacer adjacent motif (PAM) sequences: A brief overview
•PAM sequences are uniquely associated with each Cas9 protein.•PAM is required to initiate base-pairing between guide RNA and DNA target.•High-throughput screening approaches allow PAM identification.•Cas9 with novel PAM requirements may expand toolbox for genome editing. Recently the Cas9, an RNA g...
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Veröffentlicht in: | Methods (San Diego, Calif.) Calif.), 2017-05, Vol.121-122, p.3-8 |
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creator | Karvelis, Tautvydas Gasiunas, Giedrius Siksnys, Virginijus |
description | •PAM sequences are uniquely associated with each Cas9 protein.•PAM is required to initiate base-pairing between guide RNA and DNA target.•High-throughput screening approaches allow PAM identification.•Cas9 with novel PAM requirements may expand toolbox for genome editing.
Recently the Cas9, an RNA guided DNA endonuclease, emerged as a powerful tool for targeted genome manipulations. Cas9 protein can be reprogrammed to cleave, bind or nick any DNA target by simply changing crRNA sequence, however a short nucleotide sequence, termed PAM, is required to initiate crRNA hybridization to the DNA target. PAM sequence is recognized by Cas9 protein and must be determined experimentally for each Cas9 variant. Exploration of Cas9 orthologs could offer a diversity of PAM sequences and novel biochemical properties that may be beneficial for genome editing applications. Here we briefly review and compare Cas9 PAM identification assays that can be adopted for other PAM-dependent CRISPR-Cas systems. |
doi_str_mv | 10.1016/j.ymeth.2017.03.006 |
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Recently the Cas9, an RNA guided DNA endonuclease, emerged as a powerful tool for targeted genome manipulations. Cas9 protein can be reprogrammed to cleave, bind or nick any DNA target by simply changing crRNA sequence, however a short nucleotide sequence, termed PAM, is required to initiate crRNA hybridization to the DNA target. PAM sequence is recognized by Cas9 protein and must be determined experimentally for each Cas9 variant. Exploration of Cas9 orthologs could offer a diversity of PAM sequences and novel biochemical properties that may be beneficial for genome editing applications. Here we briefly review and compare Cas9 PAM identification assays that can be adopted for other PAM-dependent CRISPR-Cas systems.</description><identifier>ISSN: 1046-2023</identifier><identifier>EISSN: 1095-9130</identifier><identifier>DOI: 10.1016/j.ymeth.2017.03.006</identifier><identifier>PMID: 28344037</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Base Pairing ; Base Sequence ; Cas9 ; Cell Line ; Clustered Regularly Interspaced Short Palindromic Repeats ; Computational Biology ; CRISPR ; CRISPR-Associated Protein 9 ; CRISPR-Cas Systems ; DNA - genetics ; DNA - metabolism ; Endonucleases - genetics ; Endonucleases - metabolism ; Gene Editing - methods ; Gene Library ; Genome editing ; Genome, Human ; High-throughput methods ; High-Throughput Screening Assays ; Humans ; PAM library ; Plasmids - chemistry ; Plasmids - metabolism ; RNA, Guide, CRISPR-Cas Systems - genetics ; RNA, Guide, CRISPR-Cas Systems - metabolism ; Sequence Analysis, DNA</subject><ispartof>Methods (San Diego, Calif.), 2017-05, Vol.121-122, p.3-8</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-f2136c2161cb2788498366f5c256b5de3c1d90670c8ccaead747b5c769e313273</citedby><cites>FETCH-LOGICAL-c425t-f2136c2161cb2788498366f5c256b5de3c1d90670c8ccaead747b5c769e313273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ymeth.2017.03.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28344037$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karvelis, Tautvydas</creatorcontrib><creatorcontrib>Gasiunas, Giedrius</creatorcontrib><creatorcontrib>Siksnys, Virginijus</creatorcontrib><title>Methods for decoding Cas9 protospacer adjacent motif (PAM) sequences: A brief overview</title><title>Methods (San Diego, Calif.)</title><addtitle>Methods</addtitle><description>•PAM sequences are uniquely associated with each Cas9 protein.•PAM is required to initiate base-pairing between guide RNA and DNA target.•High-throughput screening approaches allow PAM identification.•Cas9 with novel PAM requirements may expand toolbox for genome editing.
Recently the Cas9, an RNA guided DNA endonuclease, emerged as a powerful tool for targeted genome manipulations. Cas9 protein can be reprogrammed to cleave, bind or nick any DNA target by simply changing crRNA sequence, however a short nucleotide sequence, termed PAM, is required to initiate crRNA hybridization to the DNA target. PAM sequence is recognized by Cas9 protein and must be determined experimentally for each Cas9 variant. Exploration of Cas9 orthologs could offer a diversity of PAM sequences and novel biochemical properties that may be beneficial for genome editing applications. Here we briefly review and compare Cas9 PAM identification assays that can be adopted for other PAM-dependent CRISPR-Cas systems.</description><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Base Pairing</subject><subject>Base Sequence</subject><subject>Cas9</subject><subject>Cell Line</subject><subject>Clustered Regularly Interspaced Short Palindromic Repeats</subject><subject>Computational Biology</subject><subject>CRISPR</subject><subject>CRISPR-Associated Protein 9</subject><subject>CRISPR-Cas Systems</subject><subject>DNA - genetics</subject><subject>DNA - metabolism</subject><subject>Endonucleases - genetics</subject><subject>Endonucleases - metabolism</subject><subject>Gene Editing - methods</subject><subject>Gene Library</subject><subject>Genome editing</subject><subject>Genome, Human</subject><subject>High-throughput methods</subject><subject>High-Throughput Screening Assays</subject><subject>Humans</subject><subject>PAM library</subject><subject>Plasmids - chemistry</subject><subject>Plasmids - metabolism</subject><subject>RNA, Guide, CRISPR-Cas Systems - genetics</subject><subject>RNA, Guide, CRISPR-Cas Systems - metabolism</subject><subject>Sequence Analysis, DNA</subject><issn>1046-2023</issn><issn>1095-9130</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC0E4v0LkJCPcEhY24njIHGoKl4SCA7A1UrsDbhq6mKnRfx7XAocOc0eZndnPkKOGOQMmDyb5J89Dm85B1blIHIAuUF2GdRlVjMBm6u5kBkHLnbIXowTAGC8UttkhytRFCCqXfJyn054G2nnA7VovHWzVzpuYk3nwQ8-zhuDgTZ2knQ20N4PrqMnj6P7UxrxfYEzg_GcjmgbHHbULzEsHX4ckK2umUY8_NF98nx1-TS-ye4erm_Ho7vMFLwcso4zIQ1nkpk2JVNFrYSUXWl4KdvSojDM1iArMMqYBhtbFVVbmkrWKJjgldgnJ-u7KWwKEwfdu2hwOm1m6BdRM6VYUUilRLKKtdUEH2PATs-D65vwqRnoFVA90d9A9QqoBqET0LR1_PNg0fZo_3Z-CSbDxdqAqWaqHnQ0bkXFuoBm0Na7fx98ARe0hqU</recordid><startdate>20170515</startdate><enddate>20170515</enddate><creator>Karvelis, Tautvydas</creator><creator>Gasiunas, Giedrius</creator><creator>Siksnys, Virginijus</creator><general>Elsevier Inc</general><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></search><sort><creationdate>20170515</creationdate><title>Methods for decoding Cas9 protospacer adjacent motif (PAM) sequences: A brief overview</title><author>Karvelis, Tautvydas ; Gasiunas, Giedrius ; Siksnys, Virginijus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-f2136c2161cb2788498366f5c256b5de3c1d90670c8ccaead747b5c769e313273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Base Pairing</topic><topic>Base Sequence</topic><topic>Cas9</topic><topic>Cell Line</topic><topic>Clustered Regularly Interspaced Short Palindromic Repeats</topic><topic>Computational Biology</topic><topic>CRISPR</topic><topic>CRISPR-Associated Protein 9</topic><topic>CRISPR-Cas Systems</topic><topic>DNA - genetics</topic><topic>DNA - metabolism</topic><topic>Endonucleases - genetics</topic><topic>Endonucleases - metabolism</topic><topic>Gene Editing - methods</topic><topic>Gene Library</topic><topic>Genome editing</topic><topic>Genome, Human</topic><topic>High-throughput methods</topic><topic>High-Throughput Screening Assays</topic><topic>Humans</topic><topic>PAM library</topic><topic>Plasmids - chemistry</topic><topic>Plasmids - metabolism</topic><topic>RNA, Guide, CRISPR-Cas Systems - genetics</topic><topic>RNA, Guide, CRISPR-Cas Systems - metabolism</topic><topic>Sequence Analysis, DNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karvelis, Tautvydas</creatorcontrib><creatorcontrib>Gasiunas, Giedrius</creatorcontrib><creatorcontrib>Siksnys, Virginijus</creatorcontrib><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><jtitle>Methods (San Diego, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karvelis, Tautvydas</au><au>Gasiunas, Giedrius</au><au>Siksnys, Virginijus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methods for decoding Cas9 protospacer adjacent motif (PAM) sequences: A brief overview</atitle><jtitle>Methods (San Diego, Calif.)</jtitle><addtitle>Methods</addtitle><date>2017-05-15</date><risdate>2017</risdate><volume>121-122</volume><spage>3</spage><epage>8</epage><pages>3-8</pages><issn>1046-2023</issn><eissn>1095-9130</eissn><abstract>•PAM sequences are uniquely associated with each Cas9 protein.•PAM is required to initiate base-pairing between guide RNA and DNA target.•High-throughput screening approaches allow PAM identification.•Cas9 with novel PAM requirements may expand toolbox for genome editing.
Recently the Cas9, an RNA guided DNA endonuclease, emerged as a powerful tool for targeted genome manipulations. Cas9 protein can be reprogrammed to cleave, bind or nick any DNA target by simply changing crRNA sequence, however a short nucleotide sequence, termed PAM, is required to initiate crRNA hybridization to the DNA target. PAM sequence is recognized by Cas9 protein and must be determined experimentally for each Cas9 variant. Exploration of Cas9 orthologs could offer a diversity of PAM sequences and novel biochemical properties that may be beneficial for genome editing applications. Here we briefly review and compare Cas9 PAM identification assays that can be adopted for other PAM-dependent CRISPR-Cas systems.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28344037</pmid><doi>10.1016/j.ymeth.2017.03.006</doi><tpages>6</tpages></addata></record> |
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subjects | Bacterial Proteins - genetics Bacterial Proteins - metabolism Base Pairing Base Sequence Cas9 Cell Line Clustered Regularly Interspaced Short Palindromic Repeats Computational Biology CRISPR CRISPR-Associated Protein 9 CRISPR-Cas Systems DNA - genetics DNA - metabolism Endonucleases - genetics Endonucleases - metabolism Gene Editing - methods Gene Library Genome editing Genome, Human High-throughput methods High-Throughput Screening Assays Humans PAM library Plasmids - chemistry Plasmids - metabolism RNA, Guide, CRISPR-Cas Systems - genetics RNA, Guide, CRISPR-Cas Systems - metabolism Sequence Analysis, DNA |
title | Methods for decoding Cas9 protospacer adjacent motif (PAM) sequences: A brief overview |
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