The little big genome: the organization of mitochondrial DNA

被引:39
作者
Garcia, Iraselia [1 ]
Jones, Edith [1 ]
Ramos, Manuel [1 ]
Innis-Whitehouse, Wendy [2 ]
Gilkerson, Robert [1 ,3 ]
机构
[1] Univ Texas Rio Grande Valley, Dept Biol, 1201 West Univ Dr, Edinburg, TX 78539 USA
[2] Univ Texas Rio Grande Valley, Dept Biomed Sci, Edinburg, TX 78539 USA
[3] Univ Texas Rio Grande Valley, Dept Clin Lab Sci, 1201 West Univ Dr, Edinburg, TX 78539 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2017年 / 22卷
关键词
Mitochondria; Mitochondrial DNA; Fusion; Fission; Review; MISMATCH-REPAIR ACTIVITY; MTDNA COPY NUMBER; NF-KAPPA-B; HUMAN-CELLS; TRANSCRIPTION FACTOR; OXIDATIVE STRESS; MAMMALIAN-CELLS; GENE-EXPRESSION; MATERNAL INHERITANCE; BINDING PROTEIN;
D O I
10.2741/4511
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
The small (16,569 base pair) human mitochondrial genome plays a significant role in cell metabolism and homeostasis. Mitochondrial DNA (mtDNA) contributes to the generation of complexes which are essential to oxidative phosphorylation (OXPHOS). As such, mtDNA is directly integrated into mitochondrial biogenesis and signaling and regulates mitochondrial metabolism in concert with nuclearencoded mitochondrial factors. Mitochondria are a highly dynamic, pleiomorphic network that undergoes fission and fusion events. Within this network, mtDNAs are packaged into structures called nucleoids which are actively distributed in discrete foci within the network. This sensitive organelle is frequently disrupted by insults such as oxidants and inflammatory cytokines, and undergoes genomic damage with double-and single-strand breaks that impair its function. Collectively, mtDNA is emerging as a highly sensitive indicator of cellular stress, which is directly integrated into the mitochondrial network as a contributor of a wide range of critical signaling pathways.
引用
收藏
页码:710 / 721
页数:12
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