Mitochondrial Genetics and Disease

被引:26
作者
Area-Gomez, Estela [1 ]
Schon, Eric A. [1 ,2 ]
机构
[1] Columbia Univ Med Ctr, Dept Neurol, New York, NY USA
[2] Columbia Univ Med Ctr, Dept Genet & Dev, New York, NY USA
基金
美国国家卫生研究院;
关键词
mitodynamics; mtDNA; oxidative phosphorylation; respiratory chain; MARIE-TOOTH-DISEASE; DIFFERENTIATION-ASSOCIATED PROTEIN-1; AMYOTROPHIC-LATERAL-SCLEROSIS; SPASTIC PARAPLEGIA; ER MEMBRANES; ALZHEIMER-DISEASE; ALPHA-SYNUCLEIN; COPY NUMBER; MUTATIONS; DNA;
D O I
10.1177/0883073814539561
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Mitochondrial disease resulting in reduced bioenergetic output can be due to mutations in either nuclear DNA-encoded or mitochondrial DNA-encoded gene products. We summarize some of the underlying principles of mitochondrial genetics that impact the diagnosis and pathogenesis of mitochondrial disorders. In addition, we present a brief overview of a new frontier in the field, namely, mitochondrial dynamics, which controls organellar fusion, fission, trafficking, and positioning, and exerts mitochondrial quality control by maintaining organellar integrity and viability. Analysis of mutations in gene products associated with this latter area has opened up new vistas in the study of disorders associated with compromised energy production.
引用
收藏
页码:1208 / 1215
页数:8
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