Mitochondrial DNA damage induced autophagy, cell death, and disease.
Abstract
Mammalian mitochondria contain multiple small genomes. While these organelles have
efficient base excision removal of oxidative DNA lesions and alkylation damage, many
DNA repair systems that work on nuclear DNA damage are not active in mitochondria.
What is the fate of DNA damage in the mitochondria that cannot be repaired or that
overwhelms the repair system? Some forms of mitochondrial DNA damage can apparently
trigger mitochondrial DNA destruction, either via direct degradation or through specific
forms of autophagy, such as mitophagy. However, accumulation of certain types of mitochondrial
damage, in the absence of DNA ligase III (Lig3) or exonuclease G (EXOG), can directly
trigger cell death. This review examines the cellular effects of persistent damage
to mitochondrial genomes and discusses the very different cell fates that occur in
response to different kinds of damage.
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https://hdl.handle.net/10161/12423Collections
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Joel Meyer
Professor of Environmental Genomics in the Division of Environmental Sciences and
Policy
Dr. Meyer studies the effects of toxic agents and stressors on human and wildlife
health. He is particularly interested in understanding the mechanisms by which environmental
agents cause DNA damage, the molecular processes that organisms employ to protect
prevent and repair DNA damage, and genetic differences that may lead to increased
or decreased sensitivity to DNA damage. Mitochondrial DNA damage and repair, as well
as mitochondrial function in general, are a particular focus. He studies

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