CRISPR-Cas adaptive immune systems in Sulfolobales: genetic studies and molecular mechanisms

被引:1
作者
Zhenxiao Yu [1 ]
Suping Jiang [1 ,2 ]
Yuan Wang [1 ,2 ]
Xuhui Tian [1 ,2 ]
Pengpeng Zhao [1 ]
Jianan Xu [1 ]
Mingxia Feng [1 ]
Qunxin She [1 ]
机构
[1] CRISPR and Archaea Biology Research Center,State Key Laboratory of Microbial Technology,Shandong University
[2] State Key Laboratory of Agricultural Microbiology,College of Life Science and Technology,Huazhong Agricultural University
关键词
CRISPR-Cas; adaptation; crRNA processing; PAM-dependent DNA interference; RNA-activated Cas10 activities; spatiotemporal regulation; cOA signaling; anti-CRISPR; Sulfolobales;
D O I
暂无
中图分类号
Q78 [基因工程(遗传工程)];
学科分类号
071007 ; 0836 ; 090102 ;
摘要
CRISPR-Cas systems provide the small RNA-based adaptive immunity to defend against invasive genetic elements in archaea and bacteria. Organisms of Sulfolobales, an order of thermophilic acidophiles belonging to the Crenarchaeotal Phylum, usually contain both type I and type Ⅲ CRISPR-Cas systems. Two species, Saccharolobus solfataricus and Sulfolobus islandicus, have been important models for CRISPR study in archaea, and knowledge obtained from these studies has greatly expanded our understanding of molecular mechanisms of antiviral defense in all three steps: adaptation, expression and crRNA processing, and interference. Four subtypes of CRISPR-Cas systems are common in these organisms, including I-A, I-D, Ⅲ-B, and Ⅲ-D. These cas genes form functional modules, e.g., all genes required for adaptation and for interference in the I-A immune system are clustered together to form aCas and i Cas modules. Genetic assays have been developed to study mechanisms of adaptation and interference by different CRISPR-Cas systems in these model archaea, and these methodologies are useful in demonstration of the protospacer-adjacent motif(PAM)-dependent DNA interference by I-A interference modules and multiple interference activities by Ⅲ-B Cmr systems. Ribonucleoprotein effector complexes have been isolated for Sulfolobales Ⅲ-B and Ⅲ-D systems, and their biochemical characterization has greatly enriched the knowledge of molecular mechanisms of these novel antiviral immune responses.
引用
收藏
页码:678 / 696
页数:19
相关论文
共 117 条
[51]   Diverse CRISPR-Cas responses and dramatic cellular DNA changes and cell death in pKEF9-conjugated Sulfolobus species [J].
Liu, Guannan ;
She, Qunxin ;
Garrett, Roger A. .
NUCLEIC ACIDS RESEARCH, 2016, 44 (09) :4233-4242
[52]  
Spatiotemporal Control of Type III-A CRISPR-Cas Immunity: Coupling DNA Degradation with the Target RNA Recognition[J] . Migle Kazlauskiene,Gintautas Tamulaitis,Georgij Kostiuk,?eslovas Venclovas,Virginijus Siksnys.Molecular Cell . 2016 (2)
[53]   Structural basis for the endoribonuclease activity of the type III-A CRISPR-associated protein Csm6 [J].
Niewoehner, Ole ;
Jinek, Martin .
RNA, 2016, 22 (03) :318-329
[54]   Multiple nucleic acid cleavage modes in divergent type III CRISPR systems [J].
Zhang, Jing ;
Graham, Shirley ;
Tello, Agnes ;
Liu, Huanting ;
White, Malcolm F. .
NUCLEIC ACIDS RESEARCH, 2016, 44 (04) :1789-1799
[55]   Harnessing Type I and Type III CRISPR-Cas systems for genome editing [J].
Li, Yingjun ;
Pan, Saifu ;
Zhang, Yan ;
Ren, Min ;
Feng, Mingxia ;
Peng, Nan ;
Chen, Lanming ;
Liang, Yun Xiang ;
She, Qunxin .
NUCLEIC ACIDS RESEARCH, 2016, 44 (04)
[56]   Transcriptome changes in STSV2-infected Sulfolobus islandicusREY15A undergoing continuous CRISPR spacer acquisition [J].
Leon-Sobrino, Carlos ;
Kot, Witold P. ;
Garrett, Roger A. .
MOLECULAR MICROBIOLOGY, 2016, 99 (04) :719-728
[57]   RNA-activated DNA cleavage by the Type III-B CRISPR-Cas effector complex [J].
Estrella, Michael A. ;
Kuo, Fang-Ting ;
Bailey, Scott .
GENES & DEVELOPMENT, 2016, 30 (04) :460-470
[58]   Bipartite recognition of target RNAs activates DNA cleavage by the Type III-B CRISPR-Cas system [J].
Elmore, Joshua R. ;
Sheppard, Nolan F. ;
Ramia, Nancy ;
Deighan, Trace ;
Li, Hong ;
Terns, Rebecca M. ;
Terns, Michael P. .
GENES & DEVELOPMENT, 2016, 30 (04) :447-459
[59]   The CRISPR-associated Csx1 protein of Pyrococcus furiosus is an adenosine-specific endoribonuclease [J].
Sheppard, Nolan F. ;
Glover, Claiborne V. C., III ;
Terns, Rebecca M. ;
Terns, Michael P. .
RNA, 2016, 22 (02) :216-224
[60]  
Degradation of phage transcripts by CRISPR-associated RNases enables type III CRISPR-Cas immunity[J] . Wenyan Jiang,Poulami Samai,Luciano A. Marraffini.Cell . 2015