Exploiting CRISPR-Cas immune systems for genome editing in bacteria

被引:50
作者
Barrangou, Rodolphe [1 ]
van Pijkeren, Jan-Peter [2 ]
机构
[1] N Carolina State Univ, Dept Food Bioproc & Nutr Sci, Raleigh, NC 27695 USA
[2] Univ Wisconsin, Dept Food Sci, Madison, WI 53706 USA
关键词
SEQUENCE-SPECIFIC ANTIMICROBIALS; STREPTOCOCCUS-THERMOPHILUS; ADAPTIVE IMMUNITY; ESCHERICHIA-COLI; GENE-EXPRESSION; LACTOBACILLUS-REUTERI; DUAL-RNA; DNA; INTERFERENCE; PROKARYOTES;
D O I
10.1016/j.copbio.2015.10.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The CRISPR-Cas immune system is a DNA-encoded, RNA mediated, DNA-targeting defense mechanism, which provides sequence-specific targeting of DNA. This molecular machinery can be engineered into the sgRNA:Cas9 technology, for programmable cleavage of DNA. Following the genesis of double-stranded DNA breaks, the DNA repair machinery generates mutations at the cleavage site using various pathways. This technology has revolutionized eukaryotic genome editing, and we are at the cusp of full exploitation in bacteria. Here, we discuss the potential of CRISPR-based technologies for use in bacteria, and highlight the application of single stranded DNA recombineering combined with CRISPR-Cas selection to edit the genome of a probiotic organism. We envision that CRISPR-Cas technologies will play a key role in the development of next-generation industrial bacteria.
引用
收藏
页码:61 / 68
页数:8
相关论文
共 56 条
[1]   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
[2]   The roles of CRISPR-Cas systems in adaptive immunity and beyond [J].
Barrangou, Rodolphe .
CURRENT OPINION IN IMMUNOLOGY, 2015, 32 :36-41
[3]   CRISPR-Cas Systems: Prokaryotes Upgrade to Adaptive Immunity [J].
Barrangou, Rodolphe ;
Marraffini, Luciano A. .
MOLECULAR CELL, 2014, 54 (02) :234-244
[4]   Genomic impact of CRISPR immunization against bacteriophages [J].
Barrangou, Rodolphe ;
Coute-Monvoisin, Anne-Claire ;
Stahl, Buffy ;
Chavichvily, Isabelle ;
Damange, Florian ;
Romero, Dennis A. ;
Boyaval, Patrick ;
Fremaux, Christophe ;
Horvath, Philippe .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2013, 41 :1383-1391
[5]   CRISPR-Cas systems and RNA-guided interference [J].
Barrangou, Rodolphe .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2013, 4 (03) :267-278
[6]   CRISPR. New Horizons in Phage Resistance and Strain identification [J].
Barrangou, Rodolphe ;
Horvath, Philippe .
ANNUAL REVIEW OF FOOD SCIENCE AND TECHNOLOGY, VOL 3, 2012, 3 :143-162
[7]   Exploiting CRISPR-Cas nucleases to produce sequence-specific antimicrobials [J].
Bikard, David ;
Euler, Chad W. ;
Jiang, Wenyan ;
Nussenzweig, Philip M. ;
Goldberg, Gregory W. ;
Duportet, Xavier ;
Fischetti, Vincent A. ;
Marraffini, Luciano A. .
NATURE BIOTECHNOLOGY, 2014, 32 (11) :1146-1150
[8]   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
[9]   Guide RNA Functional Modules Direct Cas9 Activity and Orthogonality [J].
Briner, Alexandra E. ;
Donohoue, Paul D. ;
Gomaa, Ahmed A. ;
Selle, Kurt ;
Slorach, Euan M. ;
Nye, Christopher H. ;
Haurwitz, Rachel E. ;
Beisel, Chase L. ;
May, Andrew P. ;
Barrangou, Rodolphe .
MOLECULAR CELL, 2014, 56 (02) :333-339
[10]   Small CRISPR RNAs guide antiviral defense in prokaryotes [J].
Brouns, Stan J. J. ;
Jore, Matthijs M. ;
Lundgren, Magnus ;
Westra, Edze R. ;
Slijkhuis, Rik J. H. ;
Snijders, Ambrosius P. L. ;
Dickman, Mark J. ;
Makarova, Kira S. ;
Koonin, Eugene V. ;
van der Oost, John .
SCIENCE, 2008, 321 (5891) :960-964