4.5 Review

Mitochondrial protein translocases for survival and wellbeing

Journal

FEBS LETTERS
Volume 588, Issue 15, Pages 2484-2495

Publisher

WILEY
DOI: 10.1016/j.febslet.2014.05.028

Keywords

Cancer; HIF1 alpha; Mitochondrial disease; Neurodegeneration; p53; Protein biogenesis and import

Funding

  1. Foundation for Polish Science-Welcome Programme
  2. EU within the European Regional Development Fund
  3. EMBO Installation grant
  4. National Science Centre (NCN) [2011/02/B/NZ2/01402]
  5. FishMed within the EU [316125]
  6. FishMed
  7. Welcome
  8. NCN [2012/05/B/NZ3/00781]

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Mitochondria are involved in many essential cellular activities. These broad functions explicate the need for the well-orchestrated biogenesis of mitochondrial proteins to avoid death and pathological consequences, both in unicellular and more complex organisms. Yeast as a model organism has been pivotal in identifying components and mechanisms that drive the transport and sorting of nuclear-encoded mitochondrial proteins. The machinery components that are involved in the import of mitochondrial proteins are generally evolutionarily conserved within the eukaryotic kingdom. However, topological and functional differences have been observed. We review the similarities and differences in mitochondrial translocases from yeast to human. Additionally, we provide a systematic overview of the contribution of mitochondrial import machineries to human pathologies, including cancer, mitochondrial diseases, and neurodegeneration. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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