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Manipulating the segregation of human mitochondrial DNA

Mennuni, M; (2018) Manipulating the segregation of human mitochondrial DNA. Doctoral thesis (Ph.D), UCL (University College London).

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Abstract

Mitochondria contain their own DNA (mtDNA), which is tiny compared to the nuclear genome and it is present in thousands of copies in the cell. This feature can lead to the coexistence of different variants within the same cell or individual, a phenomenon known as heteroplasmy and a key characteristic of many mitochondrial disorders. Typically, these diseases manifest only when the mutant mtDNAs substantially outnumber the normal copies. Therefore, even a small increase in the proportion of wild-type mtDNA can markedly improve mitochondrial function. The level of mutant mtDNA is known to be influenced by the nuclear genome, but the exact mechanism underlying the selection is still obscure. The study of the unique behaviour of A549 cells in preferring the wild-type mtDNA has led to the identification of pathways potentially important for the selection of normal mtDNA molecules. This led to the identification of a small molecule able to decrease the mutant mtDNA in heteroplasmic cells and to significantly improve mitochondrial function. After the efficacy of the compound was proved in cybrid and fibroblast cellular models, the pathways and processes affected by the compound were investigated. Both boosting the respiratory chain (RC) function and inducing ER stress appear to be necessary for the selection, but neither alone has proven to be sufficient. Moreover, the enhancement of mitochondrial function was associated with the expression of p62. The compound’s dual action of enhancing mitochondrial RC and inducing survival by activating the ER stress response, seems to be determinant in exerting a selective pressure and allow the discrimination between functional and dysfunctional mitochondria. Ultimately, the selection results from a fine tuning of selective removal of defective mitochondria by mitophagy and selective propagation of wild-type mtDNA molecules.

Type: Thesis (Doctoral)
Qualification: Ph.D
Title: Manipulating the segregation of human mitochondrial DNA
Event: UCL
Language: English
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
URI: https://discovery.ucl.ac.uk/id/eprint/10047179
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