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Illuminating the mechanisms of mitochondrial DNA quality control and inheritance

Total Cost €


EC-Contrib. €






 IlluMitoDNA project word cloud

Explore the words cloud of the IlluMitoDNA project. It provides you a very rough idea of what is the project "IlluMitoDNA" about.

first    mitochondrial    cells    quality    encoded    integrity    diseases    cell    inheritance    mtdna    understand    copies   

Project "IlluMitoDNA" data sheet

The following table provides information about the project.


Organization address
postcode: 80539

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 1˙851˙834 €
 EC max contribution 1˙851˙834 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-STG
 Funding Scheme /ERC-STG
 Starting year 2017
 Duration (year-month-day) from 2017-08-01   to  2022-07-31


Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 


 Project objective

Essential subunits of the mitochondrial respiratory chain, which generates the majority of energy in eukaryotic cells, are encoded in the mitochondrial genome (mtDNA) that is present in hundreds of copies in every cell. Mutations within mtDNA have been identified as the cause for a multitude of human diseases and have been tightly linked to the ageing process and altered stem cell homeostasis. Accordingly, to ensure organismal health, good copies of mtDNA have to be faithfully inherited during cell division, their integrity needs to be maintained over generations and they need to be distributed throughout the mitochondrial network to provide all mitochondrial segments with mtDNA encoded proteins. Astonishingly, it remains poorly understood how cells accomplish these fundamental tasks.

Through the development of a novel system that for the first time allowed minimally invasive tracking of mtDNA in living cells, we have gained unique insights into the cellular principles that govern distribution and inheritance of mtDNA and the maintenance of its integrity. This work paved the way to understand the molecular mechanisms that underlie these processes and provides the tools required to elucidate them. We will build on this work and combine cutting-edge microscopy and next generation sequencing with biochemical and genetic approaches to identify and characterize the machineries responsible for (1) mtDNA inheritance and distribution and (2) mtDNA quality control. While these first two aims will exploit the unique experimental advantages of S. cerevisiae, our ultimate goal is (3) to transfer our findings to higher eukaryotes through the development of a mammalian mtDNA imaging system.

This powerful multipronged approach will mechanistically unravel mtDNA dynamics and quality control and will thus provide the necessary basis to understand diseases where these processes are dysregulated.

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The information about "ILLUMITODNA" are provided by the European Opendata Portal: CORDIS opendata.

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