EuPaGDT: a web tool tailored to design CRISPR guide RNAs for eukaryotic pathogens

被引:204
作者
Peng, Duo [1 ,2 ,3 ]
Tarleton, Rick [1 ,2 ,3 ]
机构
[1] Univ Georgia, Ctr Trop & Emerging Global Dis, Athens, GA 30602 USA
[2] Univ Georgia, Dept Cellular Biol, Athens, GA 30602 USA
[3] Univ Georgia, Inst Bioinformat, Athens, GA 30602 USA
关键词
CRISPR-Cas9; eukaryotic pathogens; genome editing; gRNA design; webserver;
D O I
10.1099/mgen.0.000033
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recent development of CRISPR-Cas9 genome editing has enabled highly efficient and versatile manipulation of a variety of organisms and adaptation of the CRISPR-Cas9 system to eukaryotic pathogens has opened new avenues for studying these otherwise hard to manipulate organisms. Here we describe a webtool, Eukaryotic Pathogen gRNA Design Tool (EuPaGDT; available at http://grna.ctegd.uga.edu), which identifies guide RNA (gRNA) in input gene(s) to guide users in arriving at well-informed and appropriate gRNA design for many eukaryotic pathogens. Flexibility in gRNA design, accommodating unique eukaryotic pathogen (gene and genome) attributes and high-throughput gRNA design are the main features that distinguish EuPaGDT from other gRNA design tools. In addition to employing an array of known principles to score and rank gRNAs, EuPaGDT implements an effective on-target search algorithm to identify gRNA targeting multi-gene families, which are highly represented in these pathogens and play important roles in host-pathogen interactions. EuPaGDT also identifies and scores microhomology sequences flanking each gRNA targeted cut-site; these sites are often essential for the microhomology-mediated end joining process used for double-stranded break repair in these organisms. EuPaGDT also assists users in designing single-stranded oligonucleotides for homology directed repair. In batch processing mode, EuPaGDT is able to process genome-scale sequences, enabling preparation of gRNA libraries for large-scale screening projects.
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页数:7
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共 23 条
[1]   Microhomology-based choice of Cas9 nuclease target sites [J].
Bae, Sangsu ;
Kweon, Jiyeon ;
Kim, Heon Seok ;
Kim, Jin-Soo .
NATURE METHODS, 2014, 11 (07) :705-706
[2]   Regulation of Gene Editing Activity Directed by Single-Stranded Oligonucleotides and CRISPR/Cas9 Systems [J].
Bialk, Pawel ;
Rivera-Torres, Natalia ;
Strouse, Bryan ;
Kmiec, Eric B. .
PLOS ONE, 2015, 10 (06)
[3]   NUCLEOTIDE-SEQUENCES IN XENOPUS 5S DNA REQUIRED FOR TRANSCRIPTION TERMINATION [J].
BOGENHAGEN, DF ;
BROWN, DD .
CELL, 1981, 24 (01) :261-270
[4]   Chromosomal translocations induced at specified loci in human stem cells [J].
Brunet, Erika ;
Simsek, Deniz ;
Tomishima, Mark ;
DeKelver, Russell ;
Choi, Vivian M. ;
Gregory, Philip ;
Urnov, Fyodor ;
Weinstock, David M. ;
Jasin, Maria .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (26) :10620-10625
[5]   Analysis of off-target effects of CRISPR/Cas-derived RNA-guided endonucleases and nickases [J].
Cho, Seung Woo ;
Kim, Sojung ;
Kim, Yongsub ;
Kweon, Jiyeon ;
Kim, Heon Seok ;
Bae, Sangsu ;
Kim, Jin-Soo .
GENOME RESEARCH, 2014, 24 (01) :132-141
[6]   NOMENCLATURE FOR INCOMPLETELY SPECIFIED BASES IN NUCLEIC-ACID SEQUENCES - RECOMMENDATIONS 1984 [J].
CORNISHBOWDEN, A .
NUCLEIC ACIDS RESEARCH, 1985, 13 (09) :3021-3030
[7]   Rational design of highly active sgRNAs for CRISPR-Cas9-mediated gene inactivation [J].
Doench, John G. ;
Hartenian, Ella ;
Graham, Daniel B. ;
Tothova, Zuzana ;
Hegde, Mudra ;
Smith, Ian ;
Sullender, Meagan ;
Ebert, Benjamin L. ;
Xavier, Ramnik J. ;
Root, David E. .
NATURE BIOTECHNOLOGY, 2014, 32 (12) :1262-U130
[8]   Improving CRISPR-Cas nuclease specificity using truncated guide RNAs [J].
Fu, Yanfang ;
Sander, Jeffry D. ;
Reyon, Deepak ;
Cascio, Vincent M. ;
Joung, J. Keith .
NATURE BIOTECHNOLOGY, 2014, 32 (03) :279-284
[9]   Genome editing in the human malaria parasite Plasmodium falciparum using the CRISPR-Cas9 system [J].
Ghorbal, Mehdi ;
Gorman, Molly ;
Macpherson, Cameron Ross ;
Martins, Rafael Miyazawa ;
Scherf, Artur ;
Lopez-Rubio, Jose-Juan .
NATURE BIOTECHNOLOGY, 2014, 32 (08) :819-821
[10]   Microhomology-mediated deletion and gene conversion in African trypanosomes [J].
Glover, Lucy ;
Jun, Junho ;
Horn, David .
NUCLEIC ACIDS RESEARCH, 2011, 39 (04) :1372-1380