Journal
PROCEEDINGS OF THE INDIAN NATIONAL SCIENCE ACADEMY
Volume 83, Issue 4, Pages 877-891Publisher
INDIAN NAT SCI ACAD
DOI: 10.16943/ptinsa/2017/49225
Keywords
-
Categories
Funding
- University Grant Commission, India
- CAS-Zoology, Banaras Hindu University
Ask authors/readers for more resources
Human mitochondria require similar to 1500 proteins for its constitutive functions. However, the mitochondrial genome is gene deficient and most of the mitochondrial proteome is nuclear encoded and transported into the organelle. Import of majority of mitochondrial proteome is mediated by presequence pathway and requires functional interplay between a subset of molecular chaperones, along with accessory factors. Although detailed analysis has been carried out in yeast system, our understanding of human mitochondrial proteome maintenance has been severely limited by the absence of significant structural and functional information on the organization TIM23 complex in humans. Recent studies have revealed the presence of multiple presequence translocases in human mitochondria that show considerable diversity in their substrate and physiological specificity. The core organization and inter-molecular interactions between these machineries seems to be evolutionary conserved. These translocases have principally diversified due to divergence of Hsp70 co-chaperones and channel component Tim17. Another important feature associated with human mitochondrial translocases, which in most cases are absent in lower eukaryotes, is its multifunctionality. Other than housekeeping protein import, human mitochondrial translocases have gained secondary functions such asinvolvment in ROS sensing and regulation of redox balance, modulation of cellular sensitivity to xenobiotic drugs, maintenance of mitochondrial DNA, assembly of respiratory complexes' and import of non-canonical mitochondrial substrates. The origin of multifunctionality is indicative towards the possibility of functional connections between mitochondrial protein import and regulation of cellular pathways; hence, opening up new avenues of future research.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available