Literature DB >> 30301847

Is mitochondrial gene expression coordinated or stochastic?

Richard G Lee1, Danielle L Rudler1, Oliver Rackham1,2, Aleksandra Filipovska3,2.   

Abstract

Mitochondrial biogenesis is intimately dependent on the coordinated expression of the nuclear and mitochondrial genomes that is necessary for the assembly and function of the respiratory complexes to produce most of the energy required by cells. Although highly compacted in animals, the mitochondrial genome and its expression are essential for survival, development, and optimal energy production. The machinery that regulates gene expression within mitochondria is localised within the same compartment and, like in their ancestors, the bacteria, this machinery does not use membrane-based compartmentalisation to order the gene expression pathway. Therefore, the lifecycle of mitochondrial RNAs from transcription through processing, maturation, translation to turnover is mediated by a gamut of RNA-binding proteins (RBPs), all contained within the mitochondrial matrix milieu. Recent discoveries indicate that multiple processes regulating RNA metabolism occur at once but since mitochondria have a new complement of RBPs, many evolved de novo from nuclear genes, we are left wondering how co-ordinated are these processes? Here, we review recently identified examples of the co-ordinated and stochastic processes that govern the mitochondrial transcriptome. These new discoveries reveal the complexity of mitochondrial gene expression and the need for its in-depth exploration to understand how these organelles can respond to the energy demands of the cell.
© 2018 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society.

Keywords:  RNA metabolism; RNA-binding proteins; protein synthesis

Mesh:

Substances:

Year:  2018        PMID: 30301847     DOI: 10.1042/BST20180174

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  7 in total

Review 1.  Manipulating and elucidating mitochondrial gene expression with engineered proteins.

Authors:  Christopher P Wallis; Louis H Scott; Aleksandra Filipovska; Oliver Rackham
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2019-12-02       Impact factor: 6.237

Review 2.  Organization and expression of the mammalian mitochondrial genome.

Authors:  Oliver Rackham; Aleksandra Filipovska
Journal:  Nat Rev Genet       Date:  2022-04-22       Impact factor: 59.581

Review 3.  Mitochondrial Protection by PARP Inhibition.

Authors:  Ferenc Gallyas; Balazs Sumegi
Journal:  Int J Mol Sci       Date:  2020-04-16       Impact factor: 5.923

4.  MitoRibo-Tag Mice Provide a Tool for In Vivo Studies of Mitoribosome Composition.

Authors:  Jakob D Busch; Miriam Cipullo; Ilian Atanassov; Ana Bratic; Eduardo Silva Ramos; Thomas Schöndorf; Xinping Li; Sarah F Pearce; Dusanka Milenkovic; Joanna Rorbach; Nils-Göran Larsson
Journal:  Cell Rep       Date:  2019-11-05       Impact factor: 9.423

Review 5.  Mitochondrial Gene Expression and Beyond-Novel Aspects of Cellular Physiology.

Authors:  Anna V Kotrys; Roman J Szczesny
Journal:  Cells       Date:  2019-12-19       Impact factor: 6.600

6.  Fidelity of translation initiation is required for coordinated respiratory complex assembly.

Authors:  Danielle L Rudler; Laetitia A Hughes; Kara L Perks; Tara R Richman; Irina Kuznetsova; Judith A Ermer; Laila N Abudulai; Anne-Marie J Shearwood; Helena M Viola; Livia C Hool; Stefan J Siira; Oliver Rackham; Aleksandra Filipovska
Journal:  Sci Adv       Date:  2019-12-20       Impact factor: 14.136

7.  Reduced mitochondrial translation prevents diet-induced metabolic dysfunction but not inflammation.

Authors:  Kara L Perks; Nicola Ferreira; Judith A Ermer; Danielle L Rudler; Tara R Richman; Giulia Rossetti; Vance B Matthews; Natalie C Ward; Oliver Rackham; Aleksandra Filipovska
Journal:  Aging (Albany NY)       Date:  2020-10-06       Impact factor: 5.682

  7 in total

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