Nuclear-Mitochondrial Interactions

被引:58
|
作者
Walker, Brittni R. [1 ]
Moraes, Carlos T. [2 ]
机构
[1] Univ Miami, Miller Sch Med, Neurosci Program, 1420 NW 9th Ave,Rm 229, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Neurol, 1420 NW 9th Ave,Rm 229, Miami, FL 33136 USA
关键词
ACTIVATED PROTEIN-KINASE; NF-KAPPA-B; INTEGRATED STRESS-RESPONSE; FOXO TRANSCRIPTION FACTORS; REACTIVE OXYGEN; GENE-EXPRESSION; DNA MUTATIONS; SIGNAL-TRANSDUCTION; EPIGENETIC MODIFICATION; MESENCHYMAL TRANSITION;
D O I
10.3390/biom12030427
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
Mitochondria, the cell's major energy producers, also act as signaling hubs, interacting with other organelles both directly and indirectly. Despite having its own circular genome, the majority of mitochondrial proteins are encoded by nuclear DNA. To respond to changes in cell physiology, the mitochondria must send signals to the nucleus, which can, in turn, upregulate gene expression to alter metabolism or initiate a stress response. This is known as retrograde signaling. A variety of stimuli and pathways fall under the retrograde signaling umbrella. Mitochondrial dysfunction has already been shown to have severe implications for human health. Disruption of retrograde signaling, whether directly associated with mitochondrial dysfunction or cellular environmental changes, may also contribute to pathological deficits. In this review, we discuss known signaling pathways between the mitochondria and the nucleus, examine the possibility of direct contacts, and identify pathological consequences of an altered relationship.
引用
收藏
页数:29
相关论文
共 50 条
  • [11] Mitochondria and the success of somatic cell nuclear transfer cloning: from nuclear-mitochondrial interactions to mitochondrial complementation and mitochondrial DNA recombination
    Hiendleder, S
    Zakhartchenko, V
    Wolf, E
    REPRODUCTION FERTILITY AND DEVELOPMENT, 2005, 17 (1-2) : 69 - 83
  • [12] Disorders of nuclear-mitochondrial intergenomic signaling
    Spinazzola, A
    Zeviani, M
    GENE, 2005, 354 : 162 - 168
  • [13] Disorders of Nuclear-Mitochondrial Intergenomic Signalling
    Massimo Zeviani
    Vittoria Petruzzella
    Rosalba Carrozzo
    Journal of Bioenergetics and Biomembranes, 1997, 29 : 121 - 130
  • [14] Disorders of nuclear-mitochondrial intergenomic signalling
    Zeviani, M
    Petruzzella, V
    Carrozzo, R
    JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1997, 29 (02) : 121 - 130
  • [15] Disorders of nuclear-mitochondrial intergenomic communication
    Spinazzola, Antonella
    Zeviani, Massimo
    BIOSCIENCE REPORTS, 2007, 27 (1-3) : 39 - 51
  • [16] Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines
    Dey, R
    Barrientos, A
    Moraes, CT
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (40) : 31520 - 31527
  • [17] Nuclear-Mitochondrial interactions influence susceptibility to HIV-associated for neurocognitive impairment
    Smieszek, S.
    Jia, P.
    Samuels, D. C.
    Zhao, Z.
    Barnholtz-Sloan, J.
    Kaur, H.
    Letendre, S.
    Ellis, R.
    Franklin, D. R.
    Hulgan, T.
    Kallianpur, A.
    Bush, W. S.
    MITOCHONDRION, 2019, 46 : 247 - 255
  • [19] Petunia mitochondrial mutations and their use in studying nuclear-mitochondrial interaction
    Hauschner, H
    Yesodi, V
    Izhar, S
    Tabib, Y
    Firon, N
    PLANT MITOCHONDRIA: FROM GENE TO FUNCTION, 1998, : 159 - 163
  • [20] Nuclear-mitochondrial DNA damage and repair signaling
    Bohr, Vilhelm A.
    Scheybye-Knudsen, Morten
    Fang, Evandro Fey
    Sykora, Peter
    Croteau, Deborah
    DNA REPAIR, 2015, 28 : 141 - 141