Rice Science ›› 2019, Vol. 26 ›› Issue (2): 69-76.DOI: 10.1016/j.rsci.2019.01.001
• • 下一篇
收稿日期:
2018-11-21
接受日期:
2019-01-08
出版日期:
2019-03-04
发布日期:
2018-12-18
. [J]. Rice Science, 2019, 26(2): 69-76.
Property/Tool | PAM | Target gene | Reference |
CRISPR/SpCas9 | NGG | OsPDS, OsBADH2, Os02g23823, OsMPK2 | Shan et al, 2013 |
OsMPK5 | Xie et al, 2013 | ||
OsPDS, OsPMS3, OsEPSPS, OsDERF1, OsMSH1, OsMYB5, OsMYB1, OsROC5, OsSPP, OsYSA | Zhang et al, 2014 | ||
OsFTL11, Os07g0261200, Os02g0700600, OsGSTU, OsMRP15, OsWaxy | Ma et al, 2015 | ||
OsPDS, Os02g23823, OsMPK2 | Wang et al, 2015 | ||
OsPDS, OsYSA, OsDEP1 | Tang et al, 2016 | ||
OsBADH2, OsDEP1, OsGn1a, OsGS3, OsGW2, OsHd1, OsEP3, OsLPA1 | Shen et al, 2017a | ||
OsMPK5, OsPDS, OsMPK2, OsMPK1 | Ding et al, 2018 | ||
NAG | OsRAD51A, OsDMC1, OsNAL1, OsLPA1, OsLG1, OsGL1-1 | Meng et al, 2018 | |
CRISPR/SpCas9-VQR | NGA | OsNAL1, OsLPA1, OsLG1, OsGL1-1 | Hu et al, 2016 |
CRISPR/SpCas9-VRER | NGCG | OsNAL1, OsLG1, OsGL1-1 | Hu et al, 2016 |
CRISPR/SaCas9 | NNGRRT | OsDL, OsCYP72A33, OsCYP72A32, OsVIP1, OsVIP1-like gene | Kaya et al, 2016 |
CRISPR/FnCpf1 | TTN | OsDL, OsALS | Endo et al, 2016 |
OsRLK-798, OsRLK-799, OsRLK-802, OsRLK-803 | Wang et al, 2017b | ||
OsPDS, OsMPK2, OsMPK5 | Ding et al, 2018 | ||
CRISPR/LbCpf1 | TTTN | OsBEL-230, OsBEL-240, OsBEL-250, OsBEL-260 | Wang et al, 2017b |
OsPDS, OsDEP1, OsROC5 | Tang et al, 2017 | ||
OsPDS, OsBEL | Xu et al, 2017 | ||
OsNAL1, OsLG1 | Hu et al, 2017 | ||
OsPDS, OsMPK2, OsMPK5 | Ding et al, 2018 | ||
CRISPR/AsCpf1 | TTTN | OsPDS, OsDEP1, OsROC5 | Tang et al, 2017 |
OsNAL1, OsLG1 | Hu et al, 2017 | ||
CRISPR/LbCpf1-RR | TYCV | OsPDS, OsSBEIIb | Li et al, 2018b |
OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 | ||
CCCC | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 | |
CRISPR/LbCpf1-RVR | TATG | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 |
CRISPR/FnCpf1-RR | CCCC | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 |
TYCY | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 | |
CRISPR/FnCpf1-RVR | TATG | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 |
PAM, Protospacer adjacent motif. N represents A/T/G/C base. R represents A/G base. Y represents T/C base. V represents A/C/G base. |
Table 1. CRISPR/Cas system used in rice
Property/Tool | PAM | Target gene | Reference |
CRISPR/SpCas9 | NGG | OsPDS, OsBADH2, Os02g23823, OsMPK2 | Shan et al, 2013 |
OsMPK5 | Xie et al, 2013 | ||
OsPDS, OsPMS3, OsEPSPS, OsDERF1, OsMSH1, OsMYB5, OsMYB1, OsROC5, OsSPP, OsYSA | Zhang et al, 2014 | ||
OsFTL11, Os07g0261200, Os02g0700600, OsGSTU, OsMRP15, OsWaxy | Ma et al, 2015 | ||
OsPDS, Os02g23823, OsMPK2 | Wang et al, 2015 | ||
OsPDS, OsYSA, OsDEP1 | Tang et al, 2016 | ||
OsBADH2, OsDEP1, OsGn1a, OsGS3, OsGW2, OsHd1, OsEP3, OsLPA1 | Shen et al, 2017a | ||
OsMPK5, OsPDS, OsMPK2, OsMPK1 | Ding et al, 2018 | ||
NAG | OsRAD51A, OsDMC1, OsNAL1, OsLPA1, OsLG1, OsGL1-1 | Meng et al, 2018 | |
CRISPR/SpCas9-VQR | NGA | OsNAL1, OsLPA1, OsLG1, OsGL1-1 | Hu et al, 2016 |
CRISPR/SpCas9-VRER | NGCG | OsNAL1, OsLG1, OsGL1-1 | Hu et al, 2016 |
CRISPR/SaCas9 | NNGRRT | OsDL, OsCYP72A33, OsCYP72A32, OsVIP1, OsVIP1-like gene | Kaya et al, 2016 |
CRISPR/FnCpf1 | TTN | OsDL, OsALS | Endo et al, 2016 |
OsRLK-798, OsRLK-799, OsRLK-802, OsRLK-803 | Wang et al, 2017b | ||
OsPDS, OsMPK2, OsMPK5 | Ding et al, 2018 | ||
CRISPR/LbCpf1 | TTTN | OsBEL-230, OsBEL-240, OsBEL-250, OsBEL-260 | Wang et al, 2017b |
OsPDS, OsDEP1, OsROC5 | Tang et al, 2017 | ||
OsPDS, OsBEL | Xu et al, 2017 | ||
OsNAL1, OsLG1 | Hu et al, 2017 | ||
OsPDS, OsMPK2, OsMPK5 | Ding et al, 2018 | ||
CRISPR/AsCpf1 | TTTN | OsPDS, OsDEP1, OsROC5 | Tang et al, 2017 |
OsNAL1, OsLG1 | Hu et al, 2017 | ||
CRISPR/LbCpf1-RR | TYCV | OsPDS, OsSBEIIb | Li et al, 2018b |
OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 | ||
CCCC | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 | |
CRISPR/LbCpf1-RVR | TATG | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 |
CRISPR/FnCpf1-RR | CCCC | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 |
TYCY | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 | |
CRISPR/FnCpf1-RVR | TATG | OsROC5, OsPDS, OsDEP1 | Zhong et al, 2018 |
PAM, Protospacer adjacent motif. N represents A/T/G/C base. R represents A/G base. Y represents T/C base. V represents A/C/G base. |
[1] | Bibikova M, Beumer K, Trautman J K, Carroll D.2003. Enhancing gene targeting with designed zinc finger nucleases.Science, 300: 764. |
[2] | Bogdanove A J, Voytas D F.2011. TAL effectors: Customizable proteins for DNA targeting.Science, 333: 1843. |
[3] | Cong L, Ran F A, Cox D, Lin S L, Barretto R, Habib N, Hsu P D, Wu X B, Jiang W Y, Marraffini L A, Zhang F.2013. Multiplex genome engineering using CRISPR/Cas systems.Science, 8(11): 819-823. |
[4] | Ding D, Chen K Y, Chen Y D, Li H, Xie K B.2018. Engineering introns to express RNA guides for Cas9- and Cpf1-mediated multiplex genome editing.Mol Plant, 11(4): 542-552. |
[5] | Endo A, Masafumi M, Kaya H, Toki S.2016. Efficient targeted mutagenesis of rice and tobacco genomes using Cpf1 fromFrancisella novicida. Sci Rep, 6: 38169. |
[6] | Fu Y, Foden J A, Khayter C, Maeder M L, Reyon D, Joung J K, Sander J D.2013. High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells.Nat Biotechnol, 31(9): 822-826. |
[7] | Gao L Y, Cox D B T, Yan W X, Manteiga J C, Schneider M W, Yamano T, Nishimasu H, Nureki O, Crosetto N, Zhang F.2017. Engineered Cpf1 variants with altered PAM specificities.Nat Biotechnol, 35(8): 789-792. |
[8] | Gaudelli N M, Komor A C, Rees H A, Packer M S, Badran A H, Bryson D I, Liu D R.2017. Programmable base editing of A·T to G·C in genomic DNA without DNA cleavage.Nature, 551: 464-471. |
[9] | He Y B, Zhu M, Wang L H, Wu J H, Wang Q Y, Wang R C, Zhao Y D.2018. Programmed self-elimination of the CRISPR/Cas9 construct greatly accelerates the isolation of edited and transgene-free rice plants.Mol Plant, 11(9): 1210-1213. |
[10] | Hsu P D, Scott D A, Weinstein J A, Ran F A, Konermann S, Agarwala V, Li Y, Fine E J, Wu X, Shalem O, Cradick T J, Marraffini L A, Bao G, Zhang F.2013. DNA targeting specificity of RNA-guided Cas9 nucleases.Nat Biotechnol, 31(9): 827-832. |
[11] | Hu X X, Wang C, Fu Y P, Liu Q, Jiao X Z, Wang K J.2016. Expanding the range of CRISPR/Cas9 genome editing in rice.Mol Plant, 9(6): 943-945. |
[12] | Hu X X, Wang C, Liu Q, Fu Y P, Wang K J.2017. Targeted mutagenesis in rice using CRISPR-Cpf1 system.J Genet Genom, 44(1): 71-73. |
[13] | Hu X X, Meng X B, Liu Q, Li J Y, Wang K J.2018. Increasing the efficiency of CRISPR-Cas9-VQR precise genome editing in rice.Plant Biotechnol J, 16(1): 292-297. |
[14] | Hua K, Tao X P, Yuan F T, Wang D, Zhu J K.2018a. Precise A·T to G·C base editing in the rice genome.Mol Plant, 11(4): 627-630. |
[15] | Hua K, Tao X P, Zhu J K.2018b. Expanding the base editing scope in rice by using Cas9 variants.Plant Biotechnol J, doi: 10.111/pbi.12993. |
[16] | Jiang W Y, Bikard D, Cox D, Zhang F, Marraffini L A.2013. RNA-guided editing of bacterial genomes using CRISPR-Cas systems.Nat Biotechnol, 31(3): 233-239. |
[17] | Jinek M, Chylinski K, Fonfara I, Hauer M, Doudna J A, Charpentier E.2012. A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.Science, 337: 816-821. |
[18] | Kaya H, Mikami M, Endo A, Endo M, Toki S.2016. Highly specific targeted mutagenesis in plants usingStaphylococcus aureus Cas9. Sci Rep, 6: 26871. |
[19] | Kleinstiver B P, Prew M S, Tsai S Q, Topkar V V, Nguyen N T, Zheng Z, Gonzales A P, Li Z, Peterson R T, Yeh J R, Aryee M J, Joung J K.2015. Engineered CRISPR-Cas9 nucleases with altered PAM specificities.Nature, 523: 481-485. |
[20] | Kleinstiver B P, Tsai S Q, Prew M S, Nguyen N T, Welch M M, Lopez J M, McCaw Z R, Aryee M J, Joung J K.2016. Genome-wide specificities of CRISPR-Cas Cpf1 nucleases in human cells.Nat Biotechnol, 34(8): 869-874. |
[21] | Komor A C, Kim Y B, Packer M S, Zuris J A, Liu D R.2016. Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.Nature, 533: 420-424. |
[22] | Li C, Zong Y, Wang Y P, Jin S, Zhang D B, Song Q N, Zhang R, Gao C X.2018. Expanded base editing in rice and wheat using a Cas9-adenosine deaminase fusion.Genome Biol, 19: 59. |
[23] | Li J, Meng X B, Zong Y, Chen K L, Zhang H W, Liu J X, Li J Y, Gao C X.2016. Gene replacements and insertions in rice by intron targeting using CRISPR-Cas9.Nat Plants, 2: 16139. |
[24] | Li J Y, Sun Y W, Du J L, Zhao Y D, Xia L Q.2017. Generation of targeted point mutations in rice by a modified CRISPR/Cas9 system.Mol Plant, 10(3): 526-529. |
[25] | Li S Y, Li J Y, Zhang J H, Du W M, Fu J D, Sutar S, Zhao Y D, Xia L Q.2018a. Synthesis-dependent repair of Cpf1-induced double-strand DNA breaks enables targeted gene replacement in rice.J Exp Bot, 69(20): 4715-4721. |
[26] | Li S Y, Zhang X, Wang W S, Guo X P, Wu Z C, Du W M, Zhao Y D, Xia L Q.2018b. Expanding the scope of CRISPR/Cpf1- mediated genome editing in rice.Mol Plant, 11(7): 995-998. |
[27] | Li Z X, Zhang D D, Xiong X Y, Yan B Y, Xie W, Sheen J, Li J F.2017. A potent Cas9-derived gene activator for plant and mammalian cells.Nat Plants, 3(12): 930-936. |
[28] | Lowder L G, Zhang D W, Baltes N J, Paul J W, Tang X, Zheng X L, Voytas D F, Hsieh T F, Zhang Y, Qi Y P.2015. A CRISPR/Cas9 toolbox for multiplexed plant genome editing and transcriptional regulation.Plant Physiol, 169(2): 971-985. |
[29] | Lowder L G, Zhou J P, Zhang Y X, Malzahn A, Zhong Z H, Hsieh T F, Voytas D F, Zhang Y, Qi Y P.2018. Robust transcriptional activation in plants using multiplexed CRISPR-Act2.0 and mTALE-Act systems.Mol Plant, 11(2): 245-256. |
[30] | Lu H P, Liu S M, Xu S L, Chen W Y, Zhou X, Tan Y Y, Huang J Z, Shu Q Y.2017. CRISPR-S: An active interference element for a rapid and inexpensive selection of genome-edited, transgene-free rice plants.Plant Biotechnol J, 15(11): 1371-1373. |
[31] | Lu Y, Zhu J K.2017. Precise editing of a target base in the rice genome using a modified CRISPR/Cas9 system.Mol Plant, 10(3): 523-525. |
[32] | Ma X L, Zhang Q Y, Zhu Q N, Liu W, Chen Y, Qiu R, Wang B, Yang Z F, Li H Y, Lin Y R, Xie Y Y, Shen R X, Chen S F, Wang Z, Chen Y, Guo J X, Chen L T, Zhao X C, Dong Z C, Liu Y G.2015. A robust CRISPR/Cas9 system for convenient, high- efficiency multiplex genome editing in monocot and dicot plants.Mol Plant, 8(8): 1274-1284. |
[33] | Mali P, Yang L H, Esvelt K M, Aach J, Guell M, DiCarlo J E, Norville J E, Church G M.2013. RNA-guided human genome engineering via Cas9.Science, 339: 823-826. |
[34] | Meng X B, Hu X X, Liu Q, Song X G, Gao C X, Li J Y, Wang K J.2018. Robust genome editing of CRISPR-Cas9 at NAG PAMs in rice.Sci China Life Sci, 61(1): 122-125. |
[35] | Mladenov E, Iliakis G.2011. Induction and repair of DNA double strand breaks: The increasing spectrum of non-homologous end joining pathways.Mutat Res, 711: 61-72. |
[36] | Moscou M J, Bogdanove A J.2009. A simple cipher governs DNA recognition by TAL effectors.Science, 326: 1501. |
[37] | Puchta H, Fauser F.2014. Synthetic nucleases for genome engineering in plants: Prospects for a bright future.Plant J, 78(5): 727-741. |
[38] | Shan Q W, Wang Y P, Li J, Zhang Y, Chen K L, Liang Z, Zhang K, Liu J X, Xi J J Z, Qiu J L, Gao C X.2013. Targeted genome modification of crop plants using a CRISPR-Cas system.Nat Biotechnol, 31(8): 686-688. |
[39] | Shao G N, Xie L H, Jiao G A, Wei X J, Sheng Z H, Tang S Q, Hu P S.2017. CRISPR/CAS9-mediated editing of the fragrant geneBadh2 in rice. Chin J Rice Sci, 31(2): 216-222. (in Chinese with English abstract) |
[40] | Shen L, Hua Y F, Fu Y P, Li J, Liu Q, Jiao X Z, Xin G W, Wang J J, Wang X C, Yan C J, Wang K J.2017a. Rapid generation of genetic diversity by multiplex CRISPR/Cas9 genome editing in rice.Sci China Life Sci, 60(5): 506-515. |
[41] | Shen L, Li J, Fu Y P, Wang J J, Hua Y F, Jiao X Z, Yang C J, Wang K J.2017b. Orientation improvement of grain length and grain number in rice by using CRISPR/Cas9 system.Chin J Rice Sci, 31(3): 223-231. (in Chinese with English abstract) |
[42] | Sun Y W, Zhang X, Wu C Y, He Y B, Ma Y Z, Hou H, Guo X P, Du W M, Zhao Y D, Xia L Q.2016. Engineering herbicide-resistant rice plants through CRISPR/Cas9-mediated homologous recombination of acetolactate synthase.Mol Plant, 9(4): 628-631. |
[43] | Tang X, Zheng X L, Qi Y P, Zhang D W, Cheng Y, Tang A, Voytas D F, Zhang Y.2016. A single transcript CRISPR-Cas9 system for efficient genome editing in plants.Mol Plant, 9(7): 1088-1091. |
[44] | Tang X, Lowder L G, Zhang T, Malzahn A A, Zheng X, Voytas D F, Zhong Z H, Chen Y Y, Ren Q R, Li Q, Kirkland E R, Zhang Y, Qi Y P.2017. A CRISPR-Cpf1 system for efficient genome editing and transcriptional repression in plants.Nat Plants, 3: 17018. |
[45] | Tang X, Liu G Q, Zhou J P, Ren Q R, You Q, Tian L, Xin X H, Zhong Z H, Liu B L, Zheng X L, Zhang D W, Malzahn A, Gong Z Y, Qi Y P, Zhang T, Zhang Y.2018. A large-scale whole- genome sequencing analysis reveals highly specific genome editing by both Cas9 and Cpf1 (Cas12a) nucleases in rice.Genome Biol, 19: 84. |
[46] | Terns M P, Terns R M.2011. CRISPR-based adaptive immune systems.Curr Opin Microbiol, 14(3): 321-327. |
[47] | Tsai S Q, Zheng Z L, Nguyen N T, Liebers M, Topkar V V, Thapar V, Wyvekens N, Khayter C, Iafrate A J, Le L P, Aryee M J, Joung J K.2015. GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases.Nat Biotechnol, 33(2): 187-197. |
[48] | Wang C, Shen L, Fu Y P, Yan C J, Wang K J.2015. A simple CRISPR/Cas9 system for multiplex genome editing in rice.J Genet Genom, 42(12): 703-706. |
[49] | Wang M G, Lu Y M, Botella J R, Mao Y F, Hua K, Zhu J K.2017a. Gene targeting by homology-directed repair in rice using a geminivirus-based CRISPR/Cas9 system.Mol Plant, 10(7): 1007-1010. |
[50] | Wang M G, Mao Y F, Lu Y M, Tao X P, Zhu J K.2017b. Multiplex gene editing in rice using the CRISPR-Cpf1 system.Mol Plant, 10: 1011-1013. |
[51] | Wiedenheft B, Sternberg S H, Doudna J A.2012. RNA-guided genetic silencing systems in bacteria and archaea.Nature, 482: 331-338. |
[52] | Woo J W, Kim J, Kwon S I, Corvalan C, Cho S W, Kim H, Kim S G, Kim S T, Choe S, Kim J S.2015. DNA-free genome editing in plants with preassembled CRISPR-Cas9 ribonucleoproteins.Nat Biotechnol, 33(11): 1162-1164. |
[53] | Xie K B, Yang Y N.2013. RNA-guided genome editing in plants using a CRISPR-Cas system.Mol Plant, 6(6): 1975-1983. |
[54] | Xie K B, Minkenberg B, Yang Y N.2015. Boosting CRISPR/Cas9 multiplex editing capability with the endogenous tRNA-processing system.Proc Natl Acad Sci USA, 112(11): 3570-3575. |
[55] | Xing H L, Dong L, Wang Z P, Zhang H Y, Han C Y, Liu B, Wang X C, Chen Q J.2014. A CRISPR/Cas9 toolkit for multiplex genome editing in plants.BMC Plant Biol, 14: 327. |
[56] | Xu R F, Qin R Y, Li H, Li D D, Li L, Wei P C, Yang J B.2017. Generation of targeted mutant rice using a CRISPR-Cpf1 system.Plant Biotechnol J, 15(6): 713-717. |
[57] | Yamano T, Zetsche B, Ishitani R, Zhang F, Nishimasu H, Nureki O.2017. Structural basis for the canonical and non-canonical PAM recognition by CRISPR-Cpf1.Mol Cell, 67(4): 633-645. |
[58] | Yan F, Kuang Y J, Ren B, Wang J W, Zhang D W, Lin H H, Yang B, Zhou X P, Zhou H B.2018. Highly efficient A·T to G·C base editing by Cas9n-guided tRNA adenosine deaminase in rice.Mol Plant, 11(4): 631-634. |
[59] | Zetsche B, Gootenberg J S, Abudayyeh O O, Slaymaker I M, Makarova K S, Essletzbichler P, Volz S E, Joung J, van der Oost J, Regev A, Koonin E V, Zhang F.2015. Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system.Cell, 163(3): 759-771. |
[60] | Zhang D B, Zhang H W, Li T D, Chen K L, Qiu J L, Gao C X.2017. Perfectly matched 20-nucleotide guide RNA sequences enable robust genome editing using high-fidelity SpCas9 nucleases.Genome Biol, 18(1): 191. |
[61] | Zhang H, Zhang J S, Wei P L, Zhang B T, Gou F, Feng Z Y, Mao Y F, Yang L, Zhang H, Xu N F, Zhu J K.2014. The CRISPR/Cas9 system produces specific and homozygous targeted gene editing in rice in one generation.Plant Biotechnol J, 12(6): 797-807. |
[62] | Zhong Z H, Zhang Y X, You Q, Tang X, Ren Q R, Liu S S, Yang L J, Wang Y, Liu X P, Liu B L, Zhang T, Zheng X L, Le Y, Zhang Y, Qi Y P.2018. Plant genome editing using FnCpf1 and LbCpf1 nucleases at redefined and sltered PAM sites.Mol Plant, 11(7): 999-1002. |
[63] | Zong Y, Wang Y P, Li C, Zhang R, Chen K L, Ran Y D, Qiu J L, Wang D W, Gao C X.2017. Precise base editing in rice, wheat and maize with a Cas9-cytidine deaminase fusion.Nat Biotechnol, 35(5): 438-440. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||