Engineered RNA-Interacting CRISPR Guide RNAs for Genetic Sensing and Diagnostics

被引:14
作者
Galizi, Roberto [1 ,2 ]
Duncan, John N. [3 ]
Rostain, William [3 ]
Quinn, Charlotte M. [2 ,4 ]
Storch, Marko [2 ,5 ]
Kushwaha, Manish [3 ,6 ]
Jaramillo, Alfonso [3 ,7 ]
机构
[1] Keele Univ, Ctr Appl Entomol & Parasitol, Sch Life Sci, Keele, Staffs, England
[2] Imperial Coll London, Dept Life Sci, London, England
[3] Univ Warwick, Sch Life Sci, Gibbet Hill Campus, Coventry CV4 7AL, W Midlands, England
[4] Univ Liverpool Liverpool Sch Trop Med, Dept Vector Biol, Liverpool, Merseyside, England
[5] Imperial Coll London, London Biofoundry, London, England
[6] Univ Paris Saclay, Micalis Inst, AgroParisTech, INRAE, Paris, France
[7] Univ Warwick, Warwick Integrat Synthet Biol Ctr WISB, Coventry, W Midlands, England
来源
CRISPR JOURNAL | 2020年 / 3卷 / 05期
基金
英国工程与自然科学研究理事会; 欧盟地平线“2020”; 英国生物技术与生命科学研究理事会; 欧盟第七框架计划;
关键词
SOR GENE; EXPRESSION; BACTERIAL; ACTIVATION; DESIGN; TRANSCRIPTION; CELLS; COLI;
D O I
10.1089/crispr.2020.0029
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
CRISPR guide RNAs (gRNAs) can be programmed with relative ease to allow the genetic editing of nearly any DNA or RNA sequence. Here, we propose novel molecular architectures to achieve RNA-dependent modulation of CRISPR activity in response to specific RNA molecules. We designed and tested, in both living Escherichia coli cells and cell-free assays for rapid prototyping, cis-repressed RNA-interacting guide RNA (igRNA) that switch to their active state only upon interaction with small RNA fragments or long RNA transcripts, including pathogen-derived mRNAs of medical relevance such as the human immunodeficiency virus infectivity factor. The proposed CRISPR-igRNAs are fully customizable and easily adaptable to the majority if not all the available CRISPR-Cas variants to modulate a variety of genetic functions in response to specific cellular conditions, providing orthogonal activation and increased specificity. We thereby foresee a large scope of application for therapeutic, diagnostic, and biotech applications in both prokaryotic and eukaryotic systems.
引用
收藏
页码:398 / 408
页数:11
相关论文
共 47 条
[1]   Principles for Predicting RNA Secondary Structure Design Difficulty [J].
Anderson-Lee, Jeff ;
Fisker, Eli ;
Kosaraju, Vineet ;
Wu, Michelle ;
Kong, Justin ;
Lee, Jeehyung ;
Lee, Minjae ;
Zada, Mathew ;
Treuille, Adrien ;
Das, Rhiju .
JOURNAL OF MOLECULAR BIOLOGY, 2016, 428 (05) :748-757
[2]   CRISPR provides acquired resistance against viruses in prokaryotes [J].
Barrangou, Rodolphe ;
Fremaux, Christophe ;
Deveau, Helene ;
Richards, Melissa ;
Boyaval, Patrick ;
Moineau, Sylvain ;
Romero, Dennis A. ;
Horvath, Philippe .
SCIENCE, 2007, 315 (5819) :1709-1712
[3]   Self-cleaving ribozymes of hepatitis delta virus RNA [J].
Been, MD ;
Wickham, GS .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 247 (03) :741-753
[4]   Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system [J].
Bikard, David ;
Jiang, Wenyan ;
Samai, Poulami ;
Hochschild, Ann ;
Zhang, Feng ;
Marraffini, Luciano A. .
NUCLEIC ACIDS RESEARCH, 2013, 41 (15) :7429-7437
[5]   Creating small transcription activating RNAs [J].
Chappell, James ;
Takahashi, Melissa K. ;
Lucks, Julius B. .
NATURE CHEMICAL BIOLOGY, 2015, 11 (03) :214-U165
[6]   Dynamic Imaging of Genomic Loci in Living Human Cells by an Optimized CRISPR/Cas System [J].
Chen, Baohui ;
Gilbert, Luke A. ;
Cimini, Beth A. ;
Schnitzbauer, Joerg ;
Zhang, Wei ;
Li, Gene-Wei ;
Park, Jason ;
Blackburn, Elizabeth H. ;
Weissman, Jonathan S. ;
Qi, Lei S. ;
Huang, Bo .
CELL, 2013, 155 (07) :1479-1491
[7]   Orthogonal gene knockout and activation with a catalytically active Cas9 nuclease [J].
Dahlman, James E. ;
Abudayyeh, Omar O. ;
Joung, Julia ;
Gootenberg, Jonathan S. ;
Zhang, Feng ;
Konermann, Silvana .
NATURE BIOTECHNOLOGY, 2015, 33 (11) :1159-U147
[8]   Regulatory activity revealed by dynamic correlations in gene expression noise [J].
Dunlop, Mary J. ;
Cox, Robert Sidney, III ;
Levine, Joseph H. ;
Murray, Richard M. ;
Elowitz, Michael B. .
NATURE GENETICS, 2008, 40 (12) :1493-1498
[9]   Rational design of inducible CRISPR guide RNAs for de novo assembly of transcriptional programs [J].
Ferry, Quentin R. V. ;
Lyutova, Radostina ;
Fulga, Tudor A. .
NATURE COMMUNICATIONS, 2017, 8
[10]   THE SOR GENE OF HIV-1 IS REQUIRED FOR EFFICIENT VIRUS TRANSMISSION INVITRO [J].
FISHER, AG ;
ENSOLI, B ;
IVANOFF, L ;
CHAMBERLAIN, M ;
PETTEWAY, S ;
RATNER, L ;
GALLO, RC ;
WONGSTAAL, F .
SCIENCE, 1987, 237 (4817) :888-893