METHOD FOR EDITING TARGET DNA, METHOD FOR PRODUCING CELL HAVING EDITED TARGET DNA, AND DNA EDITION SYSTEM FOR USE IN SAID METHODS
A method for editing a target DNA comprising:a step of bringing(1) a fusion protein containing a TALE and a nucleic acid base converting enzyme and(2) a CRISPR-Cas9 system containing a Cas9 protein which has lost part or all of a nuclease activity and a guide RNA thereofinto contact with a target DN...
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creator | NISHIBORI, Nahoko YOSHIMA, Tadahiko HORIGOME, Kazuhiko YAMAMOTO, Takashi SAKUMA, Tetsushi |
description | A method for editing a target DNA comprising:a step of bringing(1) a fusion protein containing a TALE and a nucleic acid base converting enzyme and(2) a CRISPR-Cas9 system containing a Cas9 protein which has lost part or all of a nuclease activity and a guide RNA thereofinto contact with a target DNA to edit a base in a target site of the target DNA by using a nucleic acid base converting enzyme activity of the fusion protein, whereina TALE recognition sequence recognized by the TALE in the fusion protein or a complementary sequence thereof is present on a 5' side of the target site via a spacer 1 having a chain length of 7 to 31 bp, anda guide RNA-target sequence recognized by the guide RNA in the CRISPR-Cas9 system is present to contain a complementary base of the target site. |
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YOSHIMA, Tadahiko ; HORIGOME, Kazuhiko ; YAMAMOTO, Takashi ; SAKUMA, Tetsushi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_EP4209588A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre ; ger</language><creationdate>2023</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS THEREOF</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>NISHIBORI, Nahoko</creatorcontrib><creatorcontrib>YOSHIMA, Tadahiko</creatorcontrib><creatorcontrib>HORIGOME, Kazuhiko</creatorcontrib><creatorcontrib>YAMAMOTO, Takashi</creatorcontrib><creatorcontrib>SAKUMA, Tetsushi</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NISHIBORI, Nahoko</au><au>YOSHIMA, Tadahiko</au><au>HORIGOME, Kazuhiko</au><au>YAMAMOTO, Takashi</au><au>SAKUMA, Tetsushi</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>METHOD FOR EDITING TARGET DNA, METHOD FOR PRODUCING CELL HAVING EDITED TARGET DNA, AND DNA EDITION SYSTEM FOR USE IN SAID METHODS</title><date>2023-07-12</date><risdate>2023</risdate><abstract>A method for editing a target DNA comprising:a step of bringing(1) a fusion protein containing a TALE and a nucleic acid base converting enzyme and(2) a CRISPR-Cas9 system containing a Cas9 protein which has lost part or all of a nuclease activity and a guide RNA thereofinto contact with a target DNA to edit a base in a target site of the target DNA by using a nucleic acid base converting enzyme activity of the fusion protein, whereina TALE recognition sequence recognized by the TALE in the fusion protein or a complementary sequence thereof is present on a 5' side of the target site via a spacer 1 having a chain length of 7 to 31 bp, anda guide RNA-target sequence recognized by the guide RNA in the CRISPR-Cas9 system is present to contain a complementary base of the target site.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS THEREOF CULTURE MEDIA ENZYMOLOGY METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPIRITS VINEGAR WINE |
title | METHOD FOR EDITING TARGET DNA, METHOD FOR PRODUCING CELL HAVING EDITED TARGET DNA, AND DNA EDITION SYSTEM FOR USE IN SAID METHODS |
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