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Insert, remove or replace: A highly advanced genome editing system using CRISPR/Cas9

Ceasar, S. Antony, Rajan, Vinothkumar, Prykhozhij, Sergey V., Berman, Jason N., Ignacimuthu, S.·2016·Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
DOI 10.1016/j.bbamcr.2016.06.009
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  1. Grissa, 2007, The CRISPRdb database and tools to display CRISPRs and to generate dictionaries of spacers and repeats, BMC Bioinf., 8, 172, 10.1186/1471-2105-8-172 · DOI · Paper page
  2. Jinek, 2012, A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity, Science, 337, 816, 10.1126/science.1225829 · DOI · Paper page
  3. Townsend, 2009, High-frequency modification of plant genes using engineered zinc-finger nucleases, Nature, 459, 442, 10.1038/nature07845 · DOI
  4. Wood, 2011, Targeted genome editing across species using ZFNs and TALENs, Science, 333, 307, 10.1126/science.1207773 · DOI
  5. Moscou, 2009, A simple cipher governs DNA recognition by TAL effectors, Science, 326, 1501, 10.1126/science.1178817 · DOI
  6. Boch, 2009, Breaking the code of DNA binding specificity of TAL-type III effectors, Science, 326, 1509, 10.1126/science.1178811 · DOI · Paper page
  7. Harrison, 2014, A CRISPR view of development, Genes Dev., 28, 1859, 10.1101/gad.248252.114 · DOI
  8. Cradick, 2013, CRISPR/Cas9 systems targeting β-globin and CCR5 genes have substantial off-target activity, Nucleic Acids Res., 10.1093/nar/gkt714 · DOI · Paper page
  9. Hsu, 2014, Development and applications of CRISPR-Cas9 for genome engineering, Cell, 157, 1262, 10.1016/j.cell.2014.05.010 · DOI · Paper page
  10. Rollins, 2015, Mechanism of foreign DNA recognition by a CRISPR RNA-guided surveillance complex from Pseudomonas aeruginosa, Nucleic Acids Res., 10.1093/nar/gkv094 · DOI
  11. Heler, 2015, Cas9 specifies functional viral targets during CRISPR-Cas adaptation, Nature, 10.1038/nature14245 · DOI
  12. Choudhary, 2015, Gene silencing by CRISPR interference in mycobacteria, Nat. Commun., 6, 10.1038/ncomms7267 · DOI
  13. Ronda, 2015, CrEdit: CRISPR mediated multi-loci gene integration in Saccharomyces cerevisiae, Microb. Cell Factories, 14, 97, 10.1186/s12934-015-0288-3 · DOI
  14. Jakočiūnas, 2015, Multiplex metabolic pathway engineering using CRISPR/Cas9 in Saccharomyces cerevisiae, Metab. Eng., 28, 213, 10.1016/j.ymben.2015.01.008 · DOI
  15. Osakabe, 2014, Genome editing with engineered nucleases in plants, Plant Cell Physiol.
  16. Zhang, 2010, High frequency targeted mutagenesis in Arabidopsis thaliana using zinc finger nucleases, Proc. Natl. Acad. Sci., 107, 12028, 10.1073/pnas.0914991107 · DOI
  17. Li, 2013, Multiplex and homologous recombination-mediated genome editing in Arabidopsis and Nicotiana benthamiana using guide RNA and Cas9, Nat. Biotechnol., 31, 688, 10.1038/nbt.2654 · DOI
  18. Nekrasov, 2013, Targeted mutagenesis in the model plant Nicotiana benthamiana using Cas9 RNA-guided endonuclease, Nat. Biotechnol., 31, 691, 10.1038/nbt.2655 · DOI
  19. Shan, 2013, Targeted genome modification of crop plants using a CRISPR-Cas system, Nat. Biotechnol., 31, 686, 10.1038/nbt.2650 · DOI · Paper page
  20. Shan, 2014, Genome editing in rice and wheat using the CRISPR/Cas system, Nat. Protoc., 9, 2395, 10.1038/nprot.2014.157 · DOI
  21. Jiang, 2013, Demonstration of CRISPR/Cas9/sgRNA-mediated targeted gene modification in Arabidopsis, tobacco, sorghum and rice, Nucleic Acids Res., 41, e188, 10.1093/nar/gkt780 · DOI
  22. Johnson, 2015, Comparative assessments of CRISPR-Cas nucleases' cleavage efficiency in planta, Plant Mol. Biol., 87, 143, 10.1007/s11103-014-0266-x · DOI
  23. Feng, 2014, Multigeneration analysis reveals the inheritance, specificity, and patterns of CRISPR/Cas-induced gene modifications in Arabidopsis, Proc. Natl. Acad. Sci. U. S. A., 111, 4632, 10.1073/pnas.1400822111 · DOI
  24. Sugano, 2014, CRISPR/Cas9-mediated targeted mutagenesis in the liverwort Marchantia polymorpha L, Plant Cell Physiol., 55, 475, 10.1093/pcp/pcu014 · DOI
  25. Woo, 2015, DNA-free genome editing in plants with preassembled CRISPR-Cas9 ribonucleoproteins, Nat. Biotechnol., 10.1038/nbt.3389 · DOI · Paper page
  26. Holt, 2010, Zinc finger nuclease-mediated CCR5 knockout hematopoietic stem cell transplantation controls HIV-1 in vivo, Nat. Biotechnol., 28, 839, 10.1038/nbt.1663 · DOI · Paper page
  27. Cong, 2013, Multiplex genome engineering using CRISPR/Cas systems, Science, 339, 819, 10.1126/science.1231143 · DOI · Paper page
  28. Hou, 2013, Efficient genome engineering in human pluripotent stem cells using Cas9 from Neisseria meningitidis, Proc. Natl. Acad. Sci., 110, 15644, 10.1073/pnas.1313587110 · DOI · Paper page
  29. Ran, 2013, Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity, Cell, 154, 1380, 10.1016/j.cell.2013.08.021 · DOI · Paper page
  30. Pinder, 2015, Nuclear domain ‘knock-in’ screen for the evaluation and identification of small molecule enhancers of CRISPR-based genome editing, Nucleic Acids Res., 43, 9379, 10.1093/nar/gkv993 · DOI
  31. Song, 2016, RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency, Nat. Commun., 7, 10548, 10.1038/ncomms10548 · DOI
  32. Hilton, 2015, Epigenome editing by a CRISPR-Cas9-based acetyltransferase activates genes from promoters and enhancers, Nat. Biotechnol., 33, 510, 10.1038/nbt.3199 · DOI
  33. Wang, 2014, Genetic screens in human cells using the CRISPR-Cas9 system, Science, 343, 80, 10.1126/science.1246981 · DOI · Paper page
  34. Tzelepis, 2015, A crispr/Cas9 drop-out screen identifies genome-wide genetic valnerubilities in acute myeloid leukaemia, Blood, 126, 554, 10.1182/blood.V126.23.554.554 · DOI
  35. Port, 2015, Systematic evaluation of Drosophila CRISPR tools reveals safe and robust alternatives to autonomous gene drives in basic research, G3 (Bethesda), 5, 1493, 10.1534/g3.115.019083 · DOI · Paper page
  36. Xu, 2015, A toolkit of CRISPR-based genome editing systems in Drosophila, J. Genet. Genomics, 42, 141, 10.1016/j.jgg.2015.02.007 · DOI
  37. Ward, 2015, Rendering the intractable more tractable: tools from Caenorhabditis elegans ripe for import into parasitic nematodes, Genetics, 201, 1279, 10.1534/genetics.115.182717 · DOI
  38. Xu, 2015, The application of CRISPR-Cas9 genome editing in Caenorhabditis elegans, J. Genet. Genomics, 42, 413, 10.1016/j.jgg.2015.06.005 · DOI
  39. Pelletier, 2015, Mouse genome engineering via CRISPR-Cas9 for study of immune function, Immunity, 42, 18, 10.1016/j.immuni.2015.01.004 · DOI
  40. Duncker, 2015, Animal and in silico models for the study of sarcomeric cardiomyopathies, Cardiovasc. Res., 105, 439, 10.1093/cvr/cvv006 · DOI
  41. Horii, 2015, Genome editing using mammalian haploid cells, Int. J. Mol. Sci., 16, 23604, 10.3390/ijms161023604 · DOI
  42. Skarnes, 2015, Is mouse embryonic stem cell technology obsolete?, Genome Biol., 16, 109, 10.1186/s13059-015-0673-6 · DOI
  43. Nakade, 2014, Microhomology-mediated end-joining-dependent integration of donor DNA in cells and animals using TALENs and CRISPR/Cas9, Nat. Commun., 5, 5560, 10.1038/ncomms6560 · DOI
  44. Nakayama, 2013, Simple and efficient CRISPR/Cas9-mediated targeted mutagenesis in Xenopus tropicalis, Genesis, 51, 835, 10.1002/dvg.22720 · DOI
  45. Wang, 2015, Targeted gene disruption in Xenopus laevis using CRISPR/Cas9, Cell Biosci., 5, 1, 10.1186/s13578-015-0006-1 · DOI
  46. Ansai, 2014, Targeted mutagenesis using CRISPR/Cas system in medaka, Biology Open, 3, 362, 10.1242/bio.20148177 · DOI
  47. Carroll, 2015, The societal opportunities and challenges of genome editing, Genome Biol., 16, 242, 10.1186/s13059-015-0812-0 · DOI
  48. Wang, 2015, Genome engineering in cattle: recent technological advancements, Chromosom. Res., 23, 17, 10.1007/s10577-014-9452-6 · DOI
  49. Grobet, 1997, A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle, Nat. Genet., 17, 71, 10.1038/ng0997-71 · DOI · Paper page
  50. Proudfoot, 2015, Genome edited sheep and cattle, Transgenic Res., 24, 147, 10.1007/s11248-014-9832-x · DOI
  51. Heo, 2015, CRISPR/Cas9 nuclease-mediated gene knock-in in bovine-induced pluripotent cells, Stem Cells Dev., 24, 393, 10.1089/scd.2014.0278 · DOI · Paper page
  52. Ni, 2014, Efficient gene knockout in goats using CRISPR/Cas9 system, PLoS One, 9, e106718, 10.1371/journal.pone.0106718 · DOI
  53. Wang, 2015, Generation of gene-modified goats targeting MSTN and FGF5 via zygote injection of CRISPR/Cas9 system, Sci. Rep., 5, 13878, 10.1038/srep13878 · DOI
  54. Hai, 2014, One-step generation of knockout pigs by zygote injection of CRISPR/Cas system, Cell Res., 24, 372, 10.1038/cr.2014.11 · DOI
  55. Zhou, 2014, Generation of CRISPR/Cas9-mediated gene-targeted pigs via somatic cell nuclear transfer, Cell. Mol. Life Sci., 72, 1175, 10.1007/s00018-014-1744-7 · DOI
  56. Lai, 2016, Generation of knock-in pigs carrying Oct4-tdTomato reporter through CRISPR/Cas9-mediated genome engineering, PLoS One, 11
  57. Peng, 2015, Production of human albumin in pigs through CRISPR/Cas9-mediated knockin of human cDNA into swine albumin locus in the zygotes, Sci. Rep., 5, 16705, 10.1038/srep16705 · DOI
  58. Zhou, 2015, Efficient generation of gene-modified pigs harboring precise orthologous human mutation via CRISPR/Cas9-induced homology-directed repair in zygotes, Hum. Mutat., 37, 110, 10.1002/humu.22913 · DOI
  59. Honda, 2015, Single-step generation of rabbits carrying a targeted allele of the tyrosinase gene using CRISPR/Cas9, Exp. Anim., 64, 31, 10.1538/expanim.14-0034 · DOI
  60. Witte, 2014, Gene inactivation using the CRISPR/Cas9 system in the nematode Pristionchus pacificus, Dev. Genes Evol.
  61. Perry, 2015, CRISPR/Cas9-mediated genome modification in the mollusc, Crepidula fornicata, Genesis, 53, 237, 10.1002/dvg.22843 · DOI
  62. Nakanishi, 2014, CRISPR/Cas-mediated targeted mutagenesis in Daphnia magna, PLoS One, 9, 10.1371/journal.pone.0098363 · DOI
  63. Martin, 2015, CRISPR/Cas9 mutagenesis reveals versatile roles of Hox genes in crustacean limb specification and evolution, Curr. Biol., 26, 14, 10.1016/j.cub.2015.11.021 · DOI
  64. Wei, 2014, Heritable genome editing with CRISPR/Cas9 in the silkworm, Bombyx mori, PLoS One, 9, e101210, 10.1371/journal.pone.0101210 · DOI
  65. Li, 2015, Outbred genome sequencing and CRISPR/Cas9 gene editing in butterflies, Nat. Commun., 6, 8212, 10.1038/ncomms9212 · DOI
  66. Gilles, 2015, Efficient CRISPR-mediated gene targeting and transgene replacement in the beetle Tribolium castaneum, Development, 142, 2832, 10.1242/dev.125054 · DOI
  67. Kistler, 2015, Genome engineering with CRISPR-Cas9 in the mosquito Aedes aegypti, Cell Rep., 11, 51, 10.1016/j.celrep.2015.03.009 · DOI
  68. Gantz, 2015, Highly efficient Cas9-mediated gene drive for population modification of the malaria vector mosquito Anopheles stephensi, Proc. Natl. Acad. Sci., 112, E6736, 10.1073/pnas.1521077112 · DOI
  69. Hammond, 2015, A CRISPR-Cas9 gene drive system targeting female reproduction in the malaria mosquito vector Anopheles gambiae, Nat. Biotechnol., 34, 1, 10.1038/nbt.3439 · DOI
  70. Che-Yi Lin, 2015, Genome editing in sea urchin embryos by using a CRISPR/Cas9 system, Dev. Biol., 409, 1
  71. Stolfi, 2014, Tissue-specific genome editing in Ciona embryos by CRISPR/Cas9, Development, 141, 4115, 10.1242/dev.114488 · DOI
  72. Square, 2015, CRISPR/Cas9-mediated mutagenesis in the sea lamprey, Petromyzon marinus: a powerful tool for understanding ancestral gene functions in vertebrates, Development, 142, 4180, 10.1242/dev.125609 · DOI
  73. Aluru, 2015, Targeted mutagenesis of aryl hydrocarbon receptor 2a and 2b genes in Atlantic killifish (Fundulus heteroclitus), Aquat. Toxicol., 158, 192, 10.1016/j.aquatox.2014.11.016 · DOI
  74. Harel, 2015, A platform for rapid exploration of aging and diseases in a naturally short-lived vertebrate, Cell, 160, 1013, 10.1016/j.cell.2015.01.038 · DOI · Paper page
  75. Flowers, 2014, Highly efficient targeted mutagenesis in axolotl using Cas9 RNA-guided nuclease, Development, 141, 2165, 10.1242/dev.105072 · DOI
  76. Hwang, 2013, Heritable and precise zebrafish genome editing using a CRISPR-Cas system, PLoS One, 8, e68708, 10.1371/journal.pone.0068708 · DOI
  77. Chang, 2013, Genome editing with RNA-guided Cas9 nuclease in zebrafish embryos, Cell Res., 23, 465, 10.1038/cr.2013.45 · DOI
  78. Jao, 2013, Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system, Proc. Natl. Acad. Sci., 110, 13904, 10.1073/pnas.1308335110 · DOI · Paper page
  79. Hruscha, 2013, Efficient CRISPR/Cas9 genome editing with low off-target effects in zebrafish, Development, 140, 4982, 10.1242/dev.099085 · DOI
  80. Irion, 2014, Precise and efficient genome editing in zebrafish using the CRISPR/Cas9 system, Development, 141, 4827, 10.1242/dev.115584 · DOI
  81. Xiao, 2013, Chromosomal deletions and inversions mediated by TALENs and CRISPR/Cas in zebrafish, Nucleic Acids Res., 10.1093/nar/gkt464 · DOI
  82. Ablain, 2015, A CRISPR/Cas9 vector system for tissue-specific gene disruption in zebrafish, Dev. Cell, 32, 756, 10.1016/j.devcel.2015.01.032 · DOI
  83. Yin, 2015, Multiplex conditional mutagenesis using transgenic expression of Cas9 and sgRNAs, Genetics, 200, 431, 10.1534/genetics.115.176917 · DOI
  84. Shah, 2015, Rapid reverse genetic screening using CRISPR in zebrafish, Nat. Methods, 12, 535, 10.1038/nmeth.3360 · DOI
  85. Varshney, 2015, High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9, Genome Res., 25, 1030, 10.1101/gr.186379.114 · DOI
  86. Long, 2015, Regulation of transcriptionally active genes via the catalytically inactive Cas9 in C. elegans and D. rerio, Cell Res., 25, 638, 10.1038/cr.2015.35 · DOI
  87. Auer, 2014, Highly efficient CRISPR/Cas9-mediated knock-in in zebrafish by homology-independent DNA repair, Genome Res., 24, 142, 10.1101/gr.161638.113 · DOI · Paper page
  88. Kimura, 2014, Efficient generation of knock-in transgenic zebrafish carrying reporter/driver genes by CRISPR/Cas9-mediated genome engineering, Sci. Rep., 4, 6545, 10.1038/srep06545 · DOI
  89. Li, 2015, Intron targeting-mediated and endogenous gene integrity-maintaining knockin in zebrafish using the CRISPR/Cas9 system, Cell Res., 25, 634, 10.1038/cr.2015.43 · DOI
  90. Hisano, 2015, Precise in-frame integration of exogenous DNA mediated by CRISPR/Cas9 system in zebrafish, Sci. Rep., 5, 8841, 10.1038/srep08841 · DOI
  91. Hoshijima, 2016, Precise editing of the zebrafish genome made simple and efficient, Dev. Cell, 36, 654, 10.1016/j.devcel.2016.02.015 · DOI
  92. Prykhozhij, 2015, CRISPR MultiTargeter: a web tool to find common and unique CRISPR single guide RNA targets in a set of similar sequences, PLoS One, 10
  93. Prykhozhij, 2016, A guide to computational tools and design strategies for genome editing experiments in zebrafish using CRISPR/Cas9, Zebrafish, 13, 70, 10.1089/zeb.2015.1158 · DOI
  94. Doench, 2014, Rational design of highly active sgRNAs for CRISPR-Cas9-mediated gene inactivation, Nat. Biotechnol., 32, 1262, 10.1038/nbt.3026 · DOI · Paper page
  95. Xu, 2015, Sequence determinants of improved CRISPR sgRNA design, Genome Res., 10.1101/gr.191452.115 · DOI · Paper page
  96. Moreno-Mateos, 2015, CRISPRscan: designing highly efficient sgRNAs for CRISPR-Cas9 targeting in vivo, Nat. Methods, 10.1038/nmeth.3543 · DOI · Paper page
  97. Wong, 2015, WU-CRISPR: characteristics of functional guide RNAs for the CRISPR/Cas9 system, Genome Biol., 16, 218, 10.1186/s13059-015-0784-0 · DOI
  98. Chari, 2015, Unraveling CRISPR-Cas9 genome engineering parameters via a library-on-library approach, Nat. Methods, 12, 1, 10.1038/nmeth.3473 · DOI
  99. Heigwer, 2014, E-CRISP: fast CRISPR target site identification, Nat. Methods, 11, 122, 10.1038/nmeth.2812 · DOI
  100. Lei, 2014, CRISPR-P: a web tool for synthetic single-guide RNA design of CRISPR-system in plants, Mol. Plant, 7, 1494, 10.1093/mp/ssu044 · DOI
  101. Naito, 2014, CRISPRdirect: software for designing CRISPR/Cas guide RNA with reduced off-target sites, Bioinformatics
  102. Montague, 2014, CHOPCHOP: a CRISPR/Cas9 and TALEN web tool for genome editing, Nucleic Acids Res., 10.1093/nar/gku410 · DOI
  103. Guo, 2015, Online high-throughput mutagenesis designer using scoring matrix of sequence-specific endonucleases, J. Integr. Bioinform., 12, 283, 10.1515/jib-2015-283 · DOI
  104. Xie, 2014, sgRNAcas9: a software package for designing CRISPR sgRNA and evaluating potential off-target cleavage sites, PLoS One, 9, e100448, 10.1371/journal.pone.0100448 · DOI
  105. Zhu, 2014, CRISPRseek: a bioconductor package to identify target-specific guide RNAs for CRISPR-Cas9 genome-editing systems, PLoS One, 9, e108424, 10.1371/journal.pone.0108424 · DOI
  106. Bae, 2014, Cas-OFFinder: a fast and versatile algorithm that searches for potential off-target sites of Cas9 RNA-guided endonucleases, Bioinformatics, 30, 1473, 10.1093/bioinformatics/btu048 · DOI · Paper page
  107. Xiao, 2014, CasOT: a genome-wide Cas9/gRNA off-target searching tool, Bioinformatics, 10.1093/bioinformatics/btt764 · DOI · Paper page
  108. O'Brien, 2014, GT-scan: identifying unique genomic targets, Bioinformatics, 30, 2673, 10.1093/bioinformatics/btu354 · DOI
  109. Guilinger, 2014, Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification, Nat. Biotechnol., 32, 577, 10.1038/nbt.2909 · DOI · Paper page
  110. Tsai, 2014, Dimeric CRISPR RNA-guided FokI nucleases for highly specific genome editing, Nat. Biotechnol., 32, 569, 10.1038/nbt.2908 · DOI · Paper page
  111. Ledford, 2015, CRISPR, the disruptor, Nature, 522, 20, 10.1038/522020a · DOI
  112. Webber, 2015, Opinion: is CRISPR-based gene drive a biocontrol silver bullet or global conservation threat?, Proc. Natl. Acad. Sci., 112, 10565, 10.1073/pnas.1514258112 · DOI
  113. Ma, 2013, A guide RNA sequence design platform for the CRISPR/Cas9 system for model organism genomes, BioMed Res. Int., 2013, 270805, 10.1155/2013/270805 · DOI
  114. Liu, 2015, CRISPR-ERA: a comprehensive design tool for CRISPR-mediated gene editing, repression and activation, Bioinformatics, 31, 3676, 10.1093/bioinformatics/btv423 · DOI
  115. Ran, 2013, Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity, Cell, 154, 1380, 10.1016/j.cell.2013.08.021 · DOI · Paper page

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Metadata

Authors
Ceasar, S. A., Rajan, V., Prykhozhij, S. V., Berman, J. N., & Ignacimuthu, S.
ORCID
Ignacimuthu, S.
Venue
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
Publisher
Elsevier BV
Published
2016-09
Volume
1863
Issue
9
Pages
2333-2344
ISSN
0167-4889
DOI
10.1016/j.bbamcr.2016.06.009
Cited by
151
References
19
Language
en
Licence
Funders
  • India-Loyola College (7LCTOI14ERI001)
  • King Saud University (ISPP#0020)

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