Unknown

Dataset Information

0

Advances in methods for reducing mitochondrial DNA disease by replacing or manipulating the mitochondrial genome.


ABSTRACT: Mitochondrial DNA (mtDNA) is a multi-copy genome whose cell copy number varies depending on tissue type. Mutations in mtDNA can cause a wide spectrum of diseases. Mutated mtDNA is often found as a subset of the total mtDNA population in a cell or tissue, a situation known as heteroplasmy. As mitochondrial dysfunction only presents after a certain level of heteroplasmy has been acquired, ways to artificially reduce or replace the mutated species have been attempted. This review addresses recent approaches and advances in this field, focusing on the prevention of pathogenic mtDNA transfer via mitochondrial donation techniques such as maternal spindle transfer and pronuclear transfer in which mutated mtDNA in the oocyte or fertilized embryo is substituted with normal copies of the mitochondrial genome. This review also discusses the molecular targeting and cleavage of pathogenic mtDNA to shift heteroplasmy using antigenomic therapy and genome engineering techniques including Zinc-finger nucleases and transcription activator-like effector nucleases. Finally, it considers CRISPR technology and the unique difficulties that mitochondrial genome editing presents.

SUBMITTER: Rai PK 

PROVIDER: S-EPMC6056713 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Advances in methods for reducing mitochondrial DNA disease by replacing or manipulating the mitochondrial genome.

Rai Pavandeep K PK   Craven Lyndsey L   Hoogewijs Kurt K   Russell Oliver M OM   Lightowlers Robert N RN  

Essays in biochemistry 20180720 3


Mitochondrial DNA (mtDNA) is a multi-copy genome whose cell copy number varies depending on tissue type. Mutations in mtDNA can cause a wide spectrum of diseases. Mutated mtDNA is often found as a subset of the total mtDNA population in a cell or tissue, a situation known as heteroplasmy. As mitochondrial dysfunction only presents after a certain level of heteroplasmy has been acquired, ways to artificially reduce or replace the mutated species have been attempted. This review addresses recent a  ...[more]

Similar Datasets

| S-EPMC2754248 | biostudies-literature
| S-EPMC5499117 | biostudies-literature
| S-EPMC6926476 | biostudies-literature
| S-EPMC7194472 | biostudies-literature
| S-EPMC8779225 | biostudies-literature
| S-EPMC10525414 | biostudies-literature
| S-EPMC5315023 | biostudies-literature
| S-EPMC4523420 | biostudies-literature
| S-EPMC7041634 | biostudies-literature
| S-EPMC4852919 | biostudies-literature