Evolutionary Genomics of Defense Systems in Archaea and Bacteria

被引:206
作者
Koonin, Eugene V. [1 ]
Makarova, Kira S. [1 ]
Wolf, Yuri I. [1 ]
机构
[1] NIH, Natl Ctr Biotechnol Informat, Natl Lib Med, Bethesda, MD 20894 USA
来源
ANNUAL REVIEW OF MICROBIOLOGY, VOL 71 | 2017年 / 71卷
关键词
antivirus defense; mobile genetic elements; innate immunity; adaptive immunity; dormancy; programmed cell death; restriction-modification; toxins-antitoxins; CRISPR-Cas; TOXIN-ANTITOXIN SYSTEMS; RESTRICTION-MODIFICATION SYSTEMS; MOBILE GENETIC ELEMENTS; CRISPR-CAS SYSTEMS; SEQUENCE-SPECIFIC ENDORIBONUCLEASES; ADAPTIVE IMMUNITY; PHAGE RESISTANCE; CRYSTAL-STRUCTURE; FUNCTIONAL-CHARACTERIZATION; MODIFICATION ENZYMES;
D O I
10.1146/annurev-micro-090816-093830
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Evolution of bacteria and archaea involves an incessant arms race against an enormous diversity of genetic parasites. Accordingly, a substantial fraction of the genes in most bacteria and archaea are dedicated to antiparasite defense. The functions of these defense systems follow several distinct strategies, including innate immunity; adaptive immunity; and dormancy induction, or programmed cell death. Recent comparative genomic studies taking advantage of the expanding database of microbial genomes and metagenomes, combined with direct experiments, resulted in the discovery of several previously unknown defense systems, including innate immunity centered on Argonaute proteins, bacteriophage exclusion, and new types of CRISPR-Cas systems of adaptive immunity. Some general principles of function and evolution of defense systems are starting to crystallize, in particular, extensive gain and loss of defense genes during the evolution of prokaryotes; formation of genomic defense islands; evolutionary connections between mobile genetic elements and defense, whereby genes of mobile elements are repeatedly recruited for defense functions; the partially selfish and addictive behavior of the defense systems; and coupling between immunity and dormancy induction/programmed cell death.
引用
收藏
页码:233 / +
页数:10
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