
Aggregation
Autophagy
Ca(2+)
Cancer
Cellular stress
c-Fos
Chaperones
c-myc
Degradation
E3 ligases
Heat shock
Hsp40
Hsp70
Hsp90
Hypoxia
IFN
IGF
Inflammation
LC3
mTor
Neurodegeneration
NFkappaB
Oxidative stress
Parkinson's
Proteases
Proteasome
Protein folding
Protein misfolding
ROS
Tau
Ubiquitin
UPR

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Caenorhabditis elegans as a model system to study intercompartmental proteostasis: Interrelation of mitochondrial function, longevity, and neurodegenerative diseases
Dev. Dyn. 2010, view full abstract in PubMed
The protein quality control system, composed of molecular chaperones and proteases, is of vital importance for the maintenance and function of the proteome and the health of the cell. To achieve this, the cellular proteostasis network integrates the protein folding machinery across all compartments of the eukaryotic cell to enable efficient communication and coordinate a rapid response of folding capacity. Quality control in the mitochondria, however, differs from its cytosolic counterpart due to its prokaryotic origin, and is entirely encoded by the nuclear genome. The control and regulatory cross-talk of mitochondrial function in cellular proteostasis is essential for cellular metabolism, organismal development, and lifespan. Consequently, mitochondrial dysfunction has dramatic effects on the development and progression of a number of neurodegenerative diseases, such as Friedreich's ataxia and Parkinson's disease. Studies using Caenorhabditis elegans as a model system have greatly contributed to our current knowledge of inter-compartmental proteostasis on the cellular and organismal levels.