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CRISPR相关的生物信息学基础 被引量:3

Fundamental of CRISPR System-related Bioinformatics
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摘要 成簇规律间隔短回文序列(clustered regularly interspaced short palindromic repeats,CRISPR)是细菌和古细菌在不断进化的过程中获得的一种适应性免疫防御机制,该结构与一些功能相关的蛋白质(CRISPR-associated,Cas)合称CRISPR-Cas系统。由于其致突变效率高、操作简单及成本较低的特点,近年来对CRISPR/Cas系统的研究获得越来越广泛的关注。该系统迅速在各领域中得到广泛应用,被认为是一种具有广阔应用前景的基因组定点改造分子工具。但是,该系统存在脱靶效应、测序数据分析等挑战。为此,许多研究者开发出各种软件解决以上问题。本文着重从生物信息学的角度出发,对CRISPR/Cas系统中sgRNA的设计软件、CRISPR全基因组筛选功能基因的测序数据分析软件以及CRISPR在生物信息学中的运用作一系统综述。 Clustered regularly interspaced short palindromic repeats( CRISPR) are an adaptive immune defense mechanism of bacteria and archaea obtained during evolution process. CRISPR and its special structure and functional associated protein( CRISPR-associated,Cas) are called CRISPR-Cas system.Due to the high efficiency,simple operation and lower cost of CRISPR/Cas system,the study of CRISPR/Cas gets more and more attention and has been applied in various fields. It is regarded as one of the promising molecule tools with broad application in genome site-directed modification. However,the system has many problems such as off-target effects and screening analysis etc. Researchers have developed a variety of software tools to solve these problems. In this paper,we reviewed the soft tools for sgRNA CRISPR/Cas system design,the CRISPR sequencing analysis,and CRISPR in the application from the aspect of the bioinformatics.
机构地区 宁波大学医学院
出处 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2016年第10期1067-1076,共10页 Chinese Journal of Biochemistry and Molecular Biology
基金 国家自然科学基金项目(No.31301084) 浙江省自然科学基金项目(No.LQ13C060002) 宁波大学2016年度研究生科技创新基金资助项目(No.g16096)~~
关键词 CRISPR 基因编辑 生物信息学 clustered regularly interspaced short palindromic repeats(CRISPR) genome editing bioinformatics
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参考文献83

  • 1Ishino 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 ]. J Bacteriol, 1987,169 ( 12 ) :5429-5433. 被引量:1
  • 2Jansen R, Embden JD, Gaastra W, et al. Identification of genes that are associated with DNA repeats in prokaryotes [ J ]. Mol Microbiol, 2002,43 ( 6 ) : 1565-1575. 被引量:1
  • 3Bolotin A, Quinquis B, Sorokin A, et al. Clustered regularly interspaced short palindrome repeats (CRISPRs) have spacers of extrachromosomal origin [ J ]. Microbiology, 2005, 151 ( Pt8 ) : 2551-2561. 被引量:1
  • 4Mojica F J, Dlez-Villasefior C, Garcta-Martnez J,et al. Intervening sequences of regularly spaced prokaryotic repeats derive from foreign genetic elements[ J]. J Mol Evol,2005,60(2) :174- 182. 被引量:1
  • 5Poureel C, Salvignol G, Vergnaud G. CRISPR elements in Yersinia pestis acquire new repeats by preferential uptake of bacteriophage DNA, and provide additional tools for evolutionary studies [ J ]. Microbiology ,2005,151 ( Pt3 ) :653-663. 被引量:1
  • 6Barrangou R, Fremaux C, Deveau H, et al. CRISPR provides acquired resistance against viruses in prokaryotes [ J ]. Science, 2007,315 ( 5819 ) : 1709-1712. 被引量:1
  • 7Marraffini LA, Sontheimer EJ. CRISPR interference limits horizontal gene transfer in staphylococci by targeting DNA [ J ]. Science,2008,322(5909) : 1843-1845. 被引量:1
  • 8Jlnek 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. 被引量:1
  • 9Cencic R, Miura H, Malina A, et al. Protospacer adjacent motif (PAM)-distal sequences engage CRISPR Cas9 DNA target cleavage[ J]. PLoS One,2014,9(10) : e109213. 被引量:1
  • 10Gasiunas G, Barrangou R, Horvath P, et al. Cas9-erRNA ribonucleoprotein complex mediates specific DNA cleavage for adaptive immunity in bacteria [ J ]. Proc Natl Acad Sci USA, 2012, 109 (39) : E2579-E2586. 被引量:1

二级参考文献37

  • 1Gaj T,Gersbach C A,Barbas C F.ZFN,TALEN,and CRISPRCas-based methods for genome engineering[J].Trends Biotechnol,2013,31(7):397-405. 被引量:1
  • 2Carroll D.Genome engineering with zinc-finger nucleases[J].Genetics,2011,188(4):773-782. 被引量:1
  • 3Cornu T I,Thibodeau-Beganny S,Guhl E,et al.DNA-binding specificity is a major determinant of the activity and toxicity of zinc-finger nucleases[J].Mol Ther,2008,16(2):352-. 被引量:1
  • 4Joung J K,Sander J D.TALENs:a widely applicable technology for targeted genome editing[J].Nat Rev Mol Cell Biol,2013,14(1):49-55. 被引量:1
  • 5Wang L,Lin J,Zhang T,et al.Simultaneous screening and validation of effective zinc finger nucleases in yeast[J].PLoS One,2013,8(5):e64687-. 被引量:1
  • 6Cong L,Ran F A,Cox D,et al.Multiplex genome engineering using CRISPRCas systems[J].Science,2013,339(6121):819-823. 被引量:1
  • 7Lin W Y,Wilson J H,Lin Y.Repair of chromosomal double-strand breaks by precise ligation in human cells[J].DNA Repair (Amst),2013,12(7):480-487. 被引量:1
  • 8Richter C,Chang J T,Fineran P C.Function and regulation of clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated (Cas) systems[J].Viruses,2012,4(10):2291-2311. 被引量:1
  • 9Westra E R,Swarts D C,Staals R H J,et al.The CRISPRs,they are a-changin':how prokaryotes generate adaptive immunity[J].Annu Rev Genet,2012,46:311-339. 被引量:1
  • 10Hsu P D,Scott D A,Weinstein J A,et al.DNA targeting specificity of RNA-guided Cas9 nucleases[J].Nat Biotechnol,2013,31(9):827-832. 被引量:1

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