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The Laboratory of Genetics and Physiology 2: Emerging Insights into the Controversial Functions of This RIG-I-Like Receptor
被引:56
作者:
Zhu, Zixiang
[1
]
Zhang, Xiangle
[1
]
Wang, Guoqing
[1
]
Zheng, Haixue
[1
]
机构:
[1] Chinese Acad Agr Sci, Lanzhou Vet Res Inst, Natl Foot & Mouth Dis Reference Lab, State Key Lab Vet Etiol Biol, Lanzhou 730046, Peoples R China
基金:
国家高技术研究发展计划(863计划);
中国国家自然科学基金;
关键词:
PATTERN-RECOGNITION RECEPTORS;
RNA HELICASE LGP2;
PARAMYXOVIRUS V PROTEINS;
INNATE IMMUNITY;
SIGNAL-TRANSDUCTION;
PATHOGEN RECOGNITION;
VIRAL REPLICATION;
CYTOSOLIC DNA;
MDA5;
SENSOR;
D O I:
10.1155/2014/960190
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The laboratory of genetics and physiology 2 (LGP2) is a key component of the RNA helicase family of retinoic acid-inducible gene 1- (RIG-I-) like receptors (RLRs) and is widely involved in viral RNA recognition and regulation during innate immune responses. Unlike RIG-I and melanoma differentiation-associated 5, both RLR members, LGP2 lacks the caspase-recruitment domain (CARD), which is required for recruiting and interacting with downstream signaling proteins to activate a cascade of downstream signaling events. The absence of the CARD results in divergent functional performance for LGP2 compared to these other RLR members. Both negative and positive regulatory roles have been reported for LGP2 in antiviral immune responses. It is currently unclear how the unusual properties of LGP2 mediate opposing roles. Future studies should elucidate the molecular mechanism(s) of LGP2 action. This minireview provides a brief overview of LGP2 structure and functions, with an expanded discussion on the regulation mechanisms in response to viral infection, hopefully stimulating insight into the divergent roles of LGP2 in the regulation of antiviral immune responses.
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页数:7
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