Concerns regarding ‘off-target’ activity of genome editing endonucleases
Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced sh...
Ausführliche Beschreibung
Autor*in: |
Kadam, Ulhas Sopanrao [verfasserIn] Shelake, Rahul Mahadev [verfasserIn] Chavhan, Rahul L. [verfasserIn] Suprasanna, Penna [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2018 |
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Schlagwörter: |
Engineered or synthetic nucleases Transcription Activator Effector-Like Nucleases (TALENs) Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) |
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Übergeordnetes Werk: |
Enthalten in: Plant physiology and biochemistry - Amsterdam [u.a.] : Elsevier Science, 1998, 131, Seite 22-30 |
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Übergeordnetes Werk: |
volume:131 ; pages:22-30 |
DOI / URN: |
10.1016/j.plaphy.2018.03.027 |
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Katalog-ID: |
ELV000346675 |
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100 | 1 | |a Kadam, Ulhas Sopanrao |e verfasserin |0 (orcid)0000-0001-8737-167X |4 aut | |
245 | 1 | 0 | |a Concerns regarding ‘off-target’ activity of genome editing endonucleases |
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520 | |a Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. | ||
650 | 4 | |a Genome editing | |
650 | 4 | |a Engineered or synthetic nucleases | |
650 | 4 | |a Zinc Finger Nucleases (ZFNs) | |
650 | 4 | |a Transcription Activator Effector-Like Nucleases (TALENs) | |
650 | 4 | |a Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) | |
650 | 4 | |a Endonucleases | |
700 | 1 | |a Shelake, Rahul Mahadev |e verfasserin |0 (orcid)0000-0003-0691-560X |4 aut | |
700 | 1 | |a Chavhan, Rahul L. |e verfasserin |4 aut | |
700 | 1 | |a Suprasanna, Penna |e verfasserin |0 (orcid)0000-0002-6572-6190 |4 aut | |
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773 | 1 | 8 | |g volume:131 |g pages:22-30 |
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912 | |a GBV_ILN_2025 | ||
912 | |a GBV_ILN_2027 | ||
912 | |a GBV_ILN_2034 | ||
912 | |a GBV_ILN_2038 | ||
912 | |a GBV_ILN_2044 | ||
912 | |a GBV_ILN_2048 | ||
912 | |a GBV_ILN_2049 | ||
912 | |a GBV_ILN_2050 | ||
912 | |a GBV_ILN_2056 | ||
912 | |a GBV_ILN_2059 | ||
912 | |a GBV_ILN_2061 | ||
912 | |a GBV_ILN_2064 | ||
912 | |a GBV_ILN_2065 | ||
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912 | |a GBV_ILN_2112 | ||
912 | |a GBV_ILN_2113 | ||
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912 | |a GBV_ILN_2522 | ||
912 | |a GBV_ILN_4035 | ||
912 | |a GBV_ILN_4037 | ||
912 | |a GBV_ILN_4112 | ||
912 | |a GBV_ILN_4125 | ||
912 | |a GBV_ILN_4126 | ||
912 | |a GBV_ILN_4242 | ||
912 | |a GBV_ILN_4251 | ||
912 | |a GBV_ILN_4305 | ||
912 | |a GBV_ILN_4313 | ||
912 | |a GBV_ILN_4323 | ||
912 | |a GBV_ILN_4324 | ||
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912 | |a GBV_ILN_4326 | ||
912 | |a GBV_ILN_4333 | ||
912 | |a GBV_ILN_4334 | ||
912 | |a GBV_ILN_4335 | ||
912 | |a GBV_ILN_4338 | ||
912 | |a GBV_ILN_4393 | ||
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allfields |
10.1016/j.plaphy.2018.03.027 doi (DE-627)ELV000346675 (ELSEVIER)S0981-9428(18)30150-5 DE-627 ger DE-627 rda eng 630 640 580 DE-600 BIODIV DE-30 fid 42.00 bkl Kadam, Ulhas Sopanrao verfasserin (orcid)0000-0001-8737-167X aut Concerns regarding ‘off-target’ activity of genome editing endonucleases 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. Genome editing Engineered or synthetic nucleases Zinc Finger Nucleases (ZFNs) Transcription Activator Effector-Like Nucleases (TALENs) Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Endonucleases Shelake, Rahul Mahadev verfasserin (orcid)0000-0003-0691-560X aut Chavhan, Rahul L. verfasserin aut Suprasanna, Penna verfasserin (orcid)0000-0002-6572-6190 aut Enthalten in Plant physiology and biochemistry Amsterdam [u.a.] : Elsevier Science, 1998 131, Seite 22-30 Online-Ressource (DE-627)324869193 (DE-600)2031431-0 (DE-576)094080925 1873-2690 nnns volume:131 pages:22-30 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 42.00 Biologie: Allgemeines AR 131 22-30 |
spelling |
10.1016/j.plaphy.2018.03.027 doi (DE-627)ELV000346675 (ELSEVIER)S0981-9428(18)30150-5 DE-627 ger DE-627 rda eng 630 640 580 DE-600 BIODIV DE-30 fid 42.00 bkl Kadam, Ulhas Sopanrao verfasserin (orcid)0000-0001-8737-167X aut Concerns regarding ‘off-target’ activity of genome editing endonucleases 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. Genome editing Engineered or synthetic nucleases Zinc Finger Nucleases (ZFNs) Transcription Activator Effector-Like Nucleases (TALENs) Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Endonucleases Shelake, Rahul Mahadev verfasserin (orcid)0000-0003-0691-560X aut Chavhan, Rahul L. verfasserin aut Suprasanna, Penna verfasserin (orcid)0000-0002-6572-6190 aut Enthalten in Plant physiology and biochemistry Amsterdam [u.a.] : Elsevier Science, 1998 131, Seite 22-30 Online-Ressource (DE-627)324869193 (DE-600)2031431-0 (DE-576)094080925 1873-2690 nnns volume:131 pages:22-30 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 42.00 Biologie: Allgemeines AR 131 22-30 |
allfields_unstemmed |
10.1016/j.plaphy.2018.03.027 doi (DE-627)ELV000346675 (ELSEVIER)S0981-9428(18)30150-5 DE-627 ger DE-627 rda eng 630 640 580 DE-600 BIODIV DE-30 fid 42.00 bkl Kadam, Ulhas Sopanrao verfasserin (orcid)0000-0001-8737-167X aut Concerns regarding ‘off-target’ activity of genome editing endonucleases 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. Genome editing Engineered or synthetic nucleases Zinc Finger Nucleases (ZFNs) Transcription Activator Effector-Like Nucleases (TALENs) Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Endonucleases Shelake, Rahul Mahadev verfasserin (orcid)0000-0003-0691-560X aut Chavhan, Rahul L. verfasserin aut Suprasanna, Penna verfasserin (orcid)0000-0002-6572-6190 aut Enthalten in Plant physiology and biochemistry Amsterdam [u.a.] : Elsevier Science, 1998 131, Seite 22-30 Online-Ressource (DE-627)324869193 (DE-600)2031431-0 (DE-576)094080925 1873-2690 nnns volume:131 pages:22-30 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 42.00 Biologie: Allgemeines AR 131 22-30 |
allfieldsGer |
10.1016/j.plaphy.2018.03.027 doi (DE-627)ELV000346675 (ELSEVIER)S0981-9428(18)30150-5 DE-627 ger DE-627 rda eng 630 640 580 DE-600 BIODIV DE-30 fid 42.00 bkl Kadam, Ulhas Sopanrao verfasserin (orcid)0000-0001-8737-167X aut Concerns regarding ‘off-target’ activity of genome editing endonucleases 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. Genome editing Engineered or synthetic nucleases Zinc Finger Nucleases (ZFNs) Transcription Activator Effector-Like Nucleases (TALENs) Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Endonucleases Shelake, Rahul Mahadev verfasserin (orcid)0000-0003-0691-560X aut Chavhan, Rahul L. verfasserin aut Suprasanna, Penna verfasserin (orcid)0000-0002-6572-6190 aut Enthalten in Plant physiology and biochemistry Amsterdam [u.a.] : Elsevier Science, 1998 131, Seite 22-30 Online-Ressource (DE-627)324869193 (DE-600)2031431-0 (DE-576)094080925 1873-2690 nnns volume:131 pages:22-30 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 42.00 Biologie: Allgemeines AR 131 22-30 |
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10.1016/j.plaphy.2018.03.027 doi (DE-627)ELV000346675 (ELSEVIER)S0981-9428(18)30150-5 DE-627 ger DE-627 rda eng 630 640 580 DE-600 BIODIV DE-30 fid 42.00 bkl Kadam, Ulhas Sopanrao verfasserin (orcid)0000-0001-8737-167X aut Concerns regarding ‘off-target’ activity of genome editing endonucleases 2018 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. Genome editing Engineered or synthetic nucleases Zinc Finger Nucleases (ZFNs) Transcription Activator Effector-Like Nucleases (TALENs) Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Endonucleases Shelake, Rahul Mahadev verfasserin (orcid)0000-0003-0691-560X aut Chavhan, Rahul L. verfasserin aut Suprasanna, Penna verfasserin (orcid)0000-0002-6572-6190 aut Enthalten in Plant physiology and biochemistry Amsterdam [u.a.] : Elsevier Science, 1998 131, Seite 22-30 Online-Ressource (DE-627)324869193 (DE-600)2031431-0 (DE-576)094080925 1873-2690 nnns volume:131 pages:22-30 GBV_USEFLAG_U SYSFLAG_U GBV_ELV FID-BIODIV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 42.00 Biologie: Allgemeines AR 131 22-30 |
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630 640 580 DE-600 BIODIV DE-30 fid 42.00 bkl Concerns regarding ‘off-target’ activity of genome editing endonucleases Genome editing Engineered or synthetic nucleases Zinc Finger Nucleases (ZFNs) Transcription Activator Effector-Like Nucleases (TALENs) Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Endonucleases |
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ddc 630 fid BIODIV bkl 42.00 misc Genome editing misc Engineered or synthetic nucleases misc Zinc Finger Nucleases (ZFNs) misc Transcription Activator Effector-Like Nucleases (TALENs) misc Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) misc Endonucleases |
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ddc 630 fid BIODIV bkl 42.00 misc Genome editing misc Engineered or synthetic nucleases misc Zinc Finger Nucleases (ZFNs) misc Transcription Activator Effector-Like Nucleases (TALENs) misc Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) misc Endonucleases |
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ddc 630 fid BIODIV bkl 42.00 misc Genome editing misc Engineered or synthetic nucleases misc Zinc Finger Nucleases (ZFNs) misc Transcription Activator Effector-Like Nucleases (TALENs) misc Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) misc Endonucleases |
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Concerns regarding ‘off-target’ activity of genome editing endonucleases |
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Concerns regarding ‘off-target’ activity of genome editing endonucleases |
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Kadam, Ulhas Sopanrao |
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Kadam, Ulhas Sopanrao Shelake, Rahul Mahadev Chavhan, Rahul L. Suprasanna, Penna |
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concerns regarding ‘off-target’ activity of genome editing endonucleases |
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Concerns regarding ‘off-target’ activity of genome editing endonucleases |
abstract |
Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. |
abstractGer |
Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. |
abstract_unstemmed |
Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system. Among these, in recent times CRISPR/Cas9 has been widely used in functional genomics and plant genetic modification. A significant concern in the application of GE tools is the occurrence of ‘off-target’ activity and induced mutations, which may impede functional analysis and gene activity studies. Moreover, the ‘off-target’ activity results in either not reported or unknown, difficult to detect, produce non-quantifiable cellular signaling and physiological effects. In the past few years, several experimental methods have been developed to identify undesired mutations and to curtail ‘off-target’ cleavage. Improvement in target specificity and minimizing ‘off-target’ activity will offer better applications of GE technology in plant biology and crop improvement. |
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Concerns regarding ‘off-target’ activity of genome editing endonucleases |
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