Role of Mutations of Mitochondrial Aminoacyl-tRNA Synthetases Genes on Epileptogenesis

被引:0
|
作者
Kong, Ling-yue [1 ]
Wu, Yi-ze [1 ]
Cheng, Run-qi [1 ]
Wang, Pei-han [1 ]
Peng, Bi-wen [1 ,2 ]
机构
[1] Wuhan Univ, Sch Basic Med Sci, Dept Physiol, Wuhan, Peoples R China
[2] Wuhan Univ, Sch Basic Med Sci, Dept Physiol, Hubei Prov Key Lab Dev Originated Dis, Donghu Rd185, Wuhan, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Mitochondrial tRNA; Aminoacyl-tRNA synthetase; Mitochondrial disorders; Epilepsy; SPINAL-CORD INVOLVEMENT; BRAIN-STEM; DEFICIENCY; FARS2; ENCEPHALOPATHY; LEUKOENCEPHALOPATHY; TRANSLATION; ACTIVATION; PHENOTYPE; FEATURES;
D O I
10.1007/s12035-023-03429-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mitochondria are the structures in cells that are responsible for producing energy. They contain a specific translation unit for synthesizing mitochondria-encoded respiratory chain components: the mitochondrial DNA (mt DNA). Recently, a growing number of syndromes associated with the dysfunction of mt DNA translation have been reported. However, the functions of these diseases still need to be precise and thus attract much attention. Mitochondrial tRNAs (mt tRNAs) are encoded by mt DNA; they are the primary cause of mitochondrial dysfunction and are associated with a wide range of pathologies. Previous research has shown the role of mt tRNAs in the epileptic mechanism. This review will focus on the function of mt tRNA and the role of mitochondrial aminoacyl-tRNA synthetase (mt aaRS) in order to summarize some common relevant mutant genes of mt aaRS that cause epilepsy and the specific symptoms of the disease they cause.
引用
收藏
页码:5482 / 5492
页数:11
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