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Molecular, cellular and organismal functions of the mitochondrial fusion machinery in animal development

Subject Area Developmental Biology
Term from 2016 to 2020
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 327062981
 
Final Report Year 2021

Final Report Abstract

Mitochondria are cellular organelles whose function is critical for cellular and organismal life throughout all eukaryotic kingdoms. Mitochondria are also highly dynamic organelles that often fuse and divide. However, to date, the functional relevance of mitochondrial dynamics is not well understood. Goal of the proposed studies is to systematically analyze the role of mitochondrial dynamics in the context of animal development. To that end, we are taking advantage of the nematode Caenorhabditis elegans, which due to its highly reproducible development is particularly amenable to studies on animal development. We have begun to analyze the development of C. elegans mutants defective in mitochondrial fusion at single cell resolution. Preliminary results suggest that these mutants exhibit defective differentiation in specific cell lineages, such as a muscle cell lineage (the D lineage). In addition, the mitochondrial unfolded protein response (UPRmt), which couples changes in the protein-folding environment in mitochondria to the expression of nuclear genes, is activated. Using a combination of cell biological, genetic and molecular approaches as well as mass-spectrometry based proteomics, we will study these two responses mechanistically and define the molecular pathways through which they are mediated.

Publications

  • 2019. Compromised Mitochondrial Protein Import Acts as a Signal for UPRmt. Cell Rep. 2019 Aug 13;28(7):1659-1669.e5
    Rolland SG, Schneid S, Schwarz M, Rackles E, Fischer C, Haeussler S, Regmi SG, Yeroslaviz A, Habermann B, Mokranjac D, Lambie E, Conradt B
    (See online at https://doi.org/10.1016/j.celrep.2019.07.049)
  • PLoS Genet. 2020. Autophagy compensates for defects in mitochondrial dynamics.2020 Mar 19;16(3):e1008638
    Haeussler S, Köhler F, Witting M, Premm MF, Rolland SG, Fischer C, Chauve L, Casanueva O, Conradt B
    (See online at https://doi.org/10.1371/journal.pgen.1008638)
 
 

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