Mitochondrial genetics, signalling and stress responses

被引:0
|
作者
Liu, Yasmine J. [1 ]
Sulc, Jonathan [1 ]
Auwerx, Johan [1 ]
机构
[1] Ecole Polytech Fed Lausanne EPFL, Lab Integrat Syst Physiol, Lausanne, Switzerland
基金
瑞士国家科学基金会; 新加坡国家研究基金会; 欧盟地平线“2020”; 欧洲研究理事会;
关键词
UNFOLDED PROTEIN RESPONSE; DNA COPY NUMBER; METABOLIC HOMEOSTASIS; LONGEVITY; HEALTH; HETEROPLASMY; COMPLEX; SIRT1; AMPK; UPR;
D O I
10.1038/s41556-025-01625-w
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondria are multifaceted organelles with crucial roles in energy generation, cellular signalling and a range of synthesis pathways. The study of mitochondrial biology is complicated by its own small genome, which is matrilineally inherited and not subject to recombination, and present in multiple, possibly different, copies. Recent methodological developments have enabled the analysis of mitochondrial DNA (mtDNA) in large-scale cohorts and highlight the far-reaching impact of mitochondrial genetic variation. Genome-editing techniques have been adapted to target mtDNA, further propelling the functional analysis of mitochondrial genes. Mitochondria are finely tuned signalling hubs, a concept that has been expanded by advances in methodologies for studying the function of mitochondrial proteins and protein complexes. Mitochondrial respiratory complexes are of dual genetic origin, requiring close coordination between mitochondrial and nuclear gene-expression systems (transcription and translation) for proper assembly and function, and recent findings highlight the importance of the mitochondria in this bidirectional signalling.
引用
收藏
页码:393 / 407
页数:15
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