Mitochondrial Base Editing: Recent Advances towards Therapeutic Opportunities

被引:11
|
作者
Kar, Bibekananda [1 ]
Castillo, Santiago R. [1 ,2 ]
Sabharwal, Ankit [1 ]
Clark, Karl J. [1 ]
Ekker, Stephen C. [1 ]
机构
[1] Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Mayo Clin, Grad Sch Biomed Sci Virol & Gene Therapy Track, Rochester 55905, MN, Afghanistan
关键词
mitochondria; mitochondrial DNA; heteroplasmy; base editing; DdCBE; TALED; DNA HETEROPLASMY; MTDNA MUTATIONS; GENE; DISEASE; CONSTRUCTION; ORGANIZATION; ELIMINATION; GENERATION; PROSPECTS; MODELS;
D O I
10.3390/ijms24065798
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
Mitochondria are critical organelles that form networks within our cells, generate energy dynamically, contribute to diverse cell and organ function, and produce a variety of critical signaling molecules, such as cortisol. This intracellular microbiome can differ between cells, tissues, and organs. Mitochondria can change with disease, age, and in response to the environment. Single nucleotide variants in the circular genomes of human mitochondrial DNA are associated with many different life-threatening diseases. Mitochondrial DNA base editing tools have established novel disease models and represent a new possibility toward personalized gene therapies for the treatment of mtDNA-based disorders.
引用
收藏
页数:25
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