Oxidative stress, mitochondrial dysfunction, and aging

H Cui, Y Kong, H Zhang - Journal of signal transduction, 2012 - Wiley Online Library
Aging is an intricate phenomenon characterized by progressive decline in physiological
functions and increase in mortality that is often accompanied by many pathological …

Maintenance and expression of mammalian mitochondrial DNA

CM Gustafsson, M Falkenberg… - Annual review of …, 2016 - annualreviews.org
Mammalian mitochondrial DNA (mtDNA) encodes 13 proteins that are essential for the
function of the oxidative phosphorylation system, which is composed of four respiratory …

[BOOK][B] Bioenergetics

DG Nicholls - 2013 - books.google.com
Extensively revised, the fourth edition of this highly successful book takes into account the
many newly determined protein structures that provide molecular insight into chemiosmotic …

[HTML][HTML] Mitochondrial genome acquisition restores respiratory function and tumorigenic potential of cancer cells without mitochondrial DNA

AS Tan, JW Baty, LF Dong, A Bezawork-Geleta… - Cell metabolism, 2015 - cell.com
We report that tumor cells without mitochondrial DNA (mtDNA) show delayed tumor growth,
and that tumor formation is associated with acquisition of mtDNA from host cells. This leads …

Mitochondrial mutations and mitoepigenetics: Focus on regulation of oxidative stress-induced responses in breast cancers

K Chen, P Lu, NM Beeraka, OA Sukocheva… - Seminars in cancer …, 2022 - Elsevier
Epigenetic regulation of mitochondrial DNA (mtDNA) is an emerging and fast-develo**
field of research. Compared to regulation of nucler DNA, mechanisms of mtDNA epigenetic …

Base-resolution map** reveals distinct m1A methylome in nuclear-and mitochondrial-encoded transcripts

X Li, X **ong, M Zhang, K Wang, Y Chen, J Zhou… - Molecular cell, 2017 - cell.com
Gene expression can be post-transcriptionally regulated via dynamic and reversible RNA
modifications. N 1-methyladenosine (m 1 A) is a recently identified mRNA modification; …

Mitochondrial DNA damage and reactive oxygen species in neurodegenerative disease

N Nissanka, CT Moraes - FEBS letters, 2018 - Wiley Online Library
Mitochondria are essential organelles within the cell where most ATP is produced through
oxidative phosphorylation (OXPHOS). A subset of the genes needed for this process are …

[HTML][HTML] Mitochondrial DNA mutations and human disease

HAL Tuppen, EL Blakely, DM Turnbull… - Biochimica et Biophysica …, 2010 - Elsevier
Mitochondrial disorders are a group of clinically heterogeneous diseases, commonly
defined by a lack of cellular energy due to oxidative phosphorylation (OXPHOS) defects …

Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA

C Kukat, CA Wurm, H Spåhr… - Proceedings of the …, 2011 - National Acad Sciences
Mammalian mtDNA is packaged in DNA-protein complexes denoted mitochondrial
nucleoids. The organization of the nucleoid is a very fundamental question in mitochondrial …

Role and mechanisms of mitophagy in liver diseases

X Ma, T McKeen, J Zhang, WX Ding - Cells, 2020 - mdpi.com
The mitochondrion is an organelle that plays a vital role in the regulation of hepatic cellular
redox, lipid metabolism, and cell death. Mitochondrial dysfunction is associated with both …