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The structural biology of type III CRISPR-Cas systems
被引:3
|作者:
Li, Xuzichao
[1
]
Han, Jie
[2
]
Yang, Jie
[1
]
Zhang, Heng
[1
]
机构:
[1] Tianjin Med Univ, Prov & Minist Cosponsored Collaborat Innovat Ctr M, Sch Basic Med Sci, Dept Biochem & Mol Biol,Minist Educ,State Key Lab, Tianjin 300070, Peoples R China
[2] Tianjin Med Univ, Sch Basic Med Sci, Dept Anat & Histol, Tianjin 300070, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CRISPR-Cas systems;
Type III CRISPR-Cas systems;
Structural biology;
RNA-SILENCING COMPLEX;
CRYSTAL-STRUCTURE;
EVOLUTIONARY CLASSIFICATION;
PROTEIN CLEAVAGE;
CMR COMPLEX;
CSM COMPLEX;
EFFECTOR;
DEFENSE;
SPECIFICITY;
RESISTANCE;
D O I:
10.1016/j.jsb.2024.108070
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
CRISPR-Cas system is an RNA-guided adaptive immune system widespread in bacteria and archaea. Among them, type III CRISPR-Cas systems are the most ancient throughout the CRISPR-Cas family, proving anti-phage defense through a crRNA-guided RNA targeting manner and possessing multiple enzymatic activities. Type III CRISPR-Cas systems comprise four typical members (type III-A to III-D) and two atypical members (type III-E and type III-F), providing immune defense through distinct mechanisms. Here, we delve into structural studies conducted on three well-characterized members: the type III-A, III-B, and III-E systems, provide an overview of the structural insights into the crRNA-guided target RNA cleavage, self/non-self discrimination, and the target RNA-dependent regulation of enzymatic subunits in the effector complex.
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页数:13
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