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Role of Mutations of Mitochondrial Aminoacyl-tRNA Synthetases Genes on Epileptogenesis.
Kong, Ling-Yue; Wu, Yi-Ze; Cheng, Run-Qi; Wang, Pei-Han; Peng, Bi-Wen.
Afiliação
  • Kong LY; Department of Physiology, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
  • Wu YZ; Department of Physiology, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
  • Cheng RQ; Department of Physiology, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
  • Wang PH; Department of Physiology, School of Basic Medical Sciences, Wuhan University, Wuhan, China.
  • Peng BW; Department of Physiology, School of Basic Medical Sciences, Wuhan University, Wuhan, China. pengbiwen@whu.edu.cn.
Mol Neurobiol ; 60(9): 5482-5492, 2023 Sep.
Article em En | MEDLINE | ID: mdl-37316759
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / Aminoacil-tRNA Sintetases Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / Aminoacil-tRNA Sintetases Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article