|本期目录/Table of Contents|

[1]徐继法,徐艳,赵吉强,等.CRISPR/Cas9系统及其在单子叶植物中的应用[J].江苏农业科学,2017,45(18):21-24.
 Xu Jifa,et al.CRISPR/Cas9 system and its application in monocot:a review[J].Jiangsu Agricultural Sciences,2017,45(18):21-24.
点击复制

CRISPR/Cas9系统及其在单子叶植物中的应用(PDF)
分享到:

《江苏农业科学》[ISSN:1002-1302/CN:32-1214/S]

卷:
第45卷
期数:
2017年18期
页码:
21-24
栏目:
专论与综述
出版日期:
2017-09-20

文章信息/Info

Title:
CRISPR/Cas9 system and its application in monocot:a review
作者:
徐继法 徐艳 赵吉强 陈磊 郭善利 宋建成
烟台大学生命科学学院,山东烟台 264005
Author(s):
Xu Jifaet al
关键词:
CRISPR/Cas9系统基因编辑技术单子叶植物植物基因组遗传育种
Keywords:
-
分类号:
Q789
DOI:
-
文献标志码:
A
摘要:
CRISPR/Cas9系统作为第3代人工核酸内切酶,已经成为继锌指核酸内切酶(zinc finger endonuclease,简称ZFNs)和类转录激活因子效应物核酸酶(transcription activator-like effector nuclease,简称TALENs)之后的新型高效定点的基因组编辑新技术。作为新型的基因编辑技术,CRISPR/Cas9系统拥有突变效率高、构建简单、花费成本低等特点,自其出现之后,受到广泛关注且得到迅速发展,给植物基因组研究和遗传育种带来革命性的变革。目前,该技术已经在多种单子叶植物中实现了基因组定点精确编辑,包括水稻(Oryza sativa)、小麦(Triticum aestivum)、玉米(Zea mays)等单子叶植物。
Abstract:
-

参考文献/References:

[1]Morton J,Davis M W,Jorgensen E M,et al. Induction and repair of zinc-nuclease-targeted double-strand breaks in somatic cells[J]. Proceedings of the National Academy of Sciences,2006,103(44):16370-16375.
[2]Durai S,Mani M,Kandavelou K,et al. Zinc finger:nucleases custom-designed molecular scissors for genome engineering of plant and mammalian cells[J]. Nucleic Acids Research,2005,33(18):5978-5990.
[3]Miller J C,Tan S Y,Qiao G J,et al. A TALE nuclease architecture for efficient genome editing[J]. Nature Biotechnology,2011,29(2):143-148.
[4]Lillestol R,Redder P,Garrett R A,et al. A putative viral defence mechansm in archaeal cells[J]. Archaea,2006,2(1):59-72.
[5]Brouns S J J,Jore M M,Lundgren M,et al. Small CRISPR RNAs guide antiviral defense in prokaryotes[J]. Science,2008,321(5891):960-964.
[6]Ishino Y,Shinagawa H,Makino K,et al. Nucleotide sequence of the iap gene,responsible for alkaline phosphatase isozyme conversion in
Escherichia coli,and identification of the gene product[J]. Journal of Bacteriology,1987,169(12):5429-5433.
[7]Chrisyian M,Cermak T,Doyle E L,et al. Targeting DNA double-strand breaks with TAL effector nucleases[J]. Genetics,2010,186(2):757-761.
[8]Carroll D,Morton J J,Beumer K J,et al. Design,construction and
in vitro testing of zinc finger nuclease[J]. Nature Protocols,2006,1(3):1329-1341.
[9]Grissa I,Vergnaud G,Pourcel C. The CRISPRdb database and tools to display CRISPRs and to generate dictionaries of spacers and repeats[J]. BMC Bioinformat,2007,8(1):172.
[10]Grissa I,Vergnaud G,Pourcel C. CRISPR finder:a web tool to identify clustered regularly interspaced short palindromic repeats[J]. Nucleic Acids Research,2007,35:52-57.
[11]Jansen R,van Embden J D A,Gaastra W,et al. Identification of genes that are associated with DNA repeats in prokaryotes[J]. Molecular microbiology,2002,43(6):1565-1575.
[12]Wei C X,Liu J Y,Yu Z S,et al. TALEN or Cas9-rapid,efficient and specific choices for genome modifications[J]. Journal of Genetics and Genomics,2013,40(6):281-289.
[13]Godde J S,Bickerton A. The repetitive DNA elements called CRISPRs and their associated genes:evidence of horizontal transfer among prokaryotes[J]. Journal of Molecular Evolution,2006,62(6):718-729.
[14]Haft D H,Selengut J,Mongodin E F,et al. A guild of 45 CRISPR-associated (Cas) protein families and multiple CRISPR/Cas9 subtypes exist in prokaryotic genomes[J]. PLoS Computational Biology,2005,1(6):e60.
[15]Makarova KS,Aravind L,Wolf Y I,et al. Unification of Cas protein families and a simple scenario for the origin and evolution of CRISPR/Cas9 systems[J]. Biology Direct,2011,6(1):38.
[16]Garneau J E,Dupuis M ,Villion M,et al. The CRISPR/Cas9 bacterial immune system cleaves bacteriophage and plasmid DNA[J]. Nature,2010,468(7320):67-71.
[17]Cong L,Ran F A,Cox D,et al. Multiple genome engineering using CRISPR/Cas9 systems[J]. Science,2013,339(6121):819-923.
[18]Qi L S,Larson M H,Gilbert L A,et al. Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression[J]. Cell,2013,152(5):1173-1183.
[19]Wang H Y,Yang H,Shivalila C S,et al. One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas9 mediated genome engineering[J]. Cell,2013,153(4):910-918.
[20]Terns M P,Terns R M. CRISPR-based adaptive immune systems[J]. Current Opinion in Microbiology,2011,14(3):321-327.
[21]Jinek M,Chylinski K,Fonfara I,et al. A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity[J]. Science,2012,337(6096):816-821.
[22]Shan Q W,Gao C X. Research progress of genome editingand derivative technologies in plants[J]. Hereditas,2015,37(10):953-973.
[23]Xie K B,Yang Y N. RNA-guided genome editing in plants using a CRISPR-Cas system[J]. Molecular Plant,2013,6(6):1975-1983.
[24]Mao Y F,Zhang H,Xu N F,et al. Application of the CRISPR-Cas system for efficient genome engineering in plants[J]. Molecular Plant,2013,6(6):2008-2011.
[25]Feng Z Y,Zhang B T,Ding W N,et al. Efficient genome editing in plants using a CRISPR/Cas9 system[J]. Cell Research,2013,23(10):1229-1232.
[26]Ma X L,Zhang Q Y,Zhu Q L,et al. A robust CRISPR/Cas9 system for convenient,high-efficiency multiplex genome editing in monocot and dicot plants[J]. Molecular Plant,2015,8(8):1274-1284.
[27]Engler C,Kandzia R,Marillonnet S. A one pot,one step,precision cloning method with high throughput capability[J]. PLoS One,2008,3(11):e3647.
[28]Gibson D G,Young L,Chuang R Y,et al. Enzymatic assembly of DNA molecules up to several hundred kilobases[J]. Nature Methods,2009,6(5):343-345.
[29]Orel N,Kyryk A,Puchta H. Different pathways of homologous recombination are used for the repair of double-strand breaks within tandemly arranged sequences in the plant genome[J]. The Plant Journal,2003,35(5):604-612.
[30]Frampton R A,Pitman A R,Fineran P C. Advances in bacteriophage-mediated control of plant pathogens[J]. International Journal of Microbiology,2012(6079):1-11.
[31]Jiang W Z,Zhou H B,Bi H H,et al. Demonstration of CRISPR/Cas9/ sgRNA-mediated targeted gene modification in
Arabidopsis,tobacco,sorghum and rice[J]. Nucleic Acids Research,2013,41(20):e188.
[32]Wang Y P,Cheng X,Shan Q W,et al. Simultaneous editing of three homoeoalleles in hexaploid bread wheat confers heritable resistance to powdery mildew[J]. Nature Biotechnology,2014,32(9):947-951.
[33]Sharma S,Upadhyay S K. Functional characterization of expressed sequence tags of bread wheat (
Triticum aestivum) and analysis of crispr binding sites for targeted genome editing[J]. American Journal of Bioinformatics Research,2014,4(1):11-22.
[34]Liang Z,Zhang K,Chen K L,et al. Targeted mutagenesis in Zea mays using TALENs and the CRISPR/Cas9 system[J]. Journal of Genetics and Genomics,2014,41(2):63-68.
[35]Xing H L,Dong L,Wang Z P,et al. A CRISPR/Cas9 toolkit for multiplex genome editing in plants[J]. BMC Plant Biology,2014,14(1):327.
[36]Zetsche B,Gootenberg J S,Abudayyeh O O,et al. Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system[J]. Cell,2015,163(3):759-771.

相似文献/References:

[1]赵盼盼,王丽,袁园园,等.提高CRISPR/Cas9系统靶向编辑效率方法的研究进展[J].江苏农业科学,2017,45(01):12.
 Zhao Panpan,et al.Research progress on methods of enhancing CRISPR/Cas9 system target editing effects[J].Jiangsu Agricultural Sciences,2017,45(18):12.
[2]李莉,任红艳,毕延震,等.基因编辑技术的新进展及展望[J].江苏农业科学,2018,46(23):5.
 Li Li,et al.New progress and prospect of gene editing technology[J].Jiangsu Agricultural Sciences,2018,46(18):5.
[3]齐世杰,赵静娟,郑怀国.基于ESI的全球作物生物育种领域研究前沿分析[J].江苏农业科学,2021,49(19):9.
 Qi Shijie,et al.Research frontier analysis of global crop biological breeding based on ESI[J].Jiangsu Agricultural Sciences,2021,49(18):9.
[4]杨海峰,甘晓雪,薄高峰,等.利用CRISPR/Cas9系统编辑银腺杨84K LAZY基因[J].江苏农业科学,2022,50(18):258.
 Yang Haifeng,et al.LAZY gene editing of Populus alba ×P. glandulosa cv. 84K by CRISPR/Cas9 system[J].Jiangsu Agricultural Sciences,2022,50(18):258.
[5]朱宗财,王志军,高能,等.CRISPR/Cas9基因编辑技术在植物抗病性改良中的应用综述[J].江苏农业科学,2024,52(3):1.
 Zhu Zongcai,et al.Application of CRISPR/Cas9 gene editing technology in improvement of plant disease resistance:a review[J].Jiangsu Agricultural Sciences,2024,52(18):1.

备注/Memo

备注/Memo:
收稿日期:2016-04-24
基金项目:国家自然科学基金(编号:3137616);山东省自然科学基金(编号:ZR2011CM044、ZR2011CM006)。
作者简介:徐继法(1987—),男,山东枣庄人,硕士,研究方向为植物分子发育生物学。E-mail:dongfengxjf@163.com。
通信作者:宋建成,博士,硕士生导师,研究方向为植物分子发育生物学。E-mail:jcsong88@yahoo.com。
更新日期/Last Update: 2017-09-20