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Modelling the mitochondrial bottleneck in vitro

Grant number: 19/07714-5
Support type:Scholarships abroad - Research Internship - Doctorate
Effective date (Start): June 17, 2019
Effective date (End): August 26, 2019
Field of knowledge:Biological Sciences - Genetics
Principal Investigator:Marcos Roberto Chiaratti
Grantee:Carolina Habermann Macabelli
Supervisor abroad: Patrick Francis Chinnery
Home Institution: Centro de Ciências Biológicas e da Saúde (CCBS). Universidade Federal de São Carlos (UFSCAR). São Carlos , SP, Brazil
Local de pesquisa : University of Cambridge, England  
Associated to the scholarship:16/07868-4 - Effect of the mitofusins knockout on the inheritance of deleterious Mitochondrial DNA in mouse embryionic fibroblasts, BP.DR

Abstract

Diseases caused by mutations in mitochondrial DNA (mtDNA) affect ~1 in 4,300 people. In addition, almost every person carries very low levels of mutated mtDNA, which may be transmitted down to the maternal lineage and associate with late-onset degenerative diseases. Transmission of mutated mtDNAs in germ cells relies upon the mitochondrial bottleneck, which results in drastic changes in the frequency of mtDNA variants within one generation. Yet, counteracting forces seem to act during specific stages of germline development to filter out pathogenic mutations in mtDNA. Mitochondria in the germline differ from those of somatic tissues by their fragmented morphology, rounded shape and small size, suggesting mitochondrial fusion is downregulated. In addition, the number of mtDNA molecules per mitochondrion is decreased in the germline to a level close to haploidy. These characteristics are expected to contribute with the bottleneck effect and the filter that prevents mutation expansion. Currently, it is challenging to estimate the mutation level that will be transmitted by a woman with mutated mtDNA. Moreover, in the case of oocytes containing high levels of mutated mtDNA, the mitochondrial replacement therapy (MRT) has been proposed as the only way of generating healthy offspring. However, this requires a healthy oocyte donor, which is challenging. In addition, pre-clinical studies with the MRT have shown unexpected 'reversion' to the original genotype in ~15% of cases. A complete understanding of the underlying mechanisms leading to shifts in the level of mutated mtDNA could be useful to generate healthy offspring, potentially avoiding the need for in vitro embryo manipulation. Hence, we propose to establish a model of the mitochondrial bottleneck based on in vitro specification of primordial germ cells (PGC)-like cells (PGCLCs) from mouse embryonic stem cells (ESCs). In addition, we will manipulate mitochondrial dynamics during PGCLC specification to assess its impact on segregation of polymorphisms and pathogenic mtDNA variants.