Differences in Strength and Timing of the mtDNA Bottleneck between Zebrafish Germline and Non-germline Cells
Auke B.C. Otten,
Tom E.J. Theunissen,
Josien G. Derhaag,
Ellen H. Lambrichs,
Iris B.W. Boesten,
Marie Winandy,
Aafke P.A. van Montfoort,
Katsiaryna Tarbashevich,
Erez Raz,
Mike Gerards,
Jo M. Vanoevelen,
Bianca J.C. van den Bosch,
Marc Muller,
Hubert J.M. Smeets
Affiliations
Auke B.C. Otten
Department of Genetics and Cell Biology, Clinical Genomics Unit, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
Tom E.J. Theunissen
Department of Genetics and Cell Biology, Clinical Genomics Unit, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
Josien G. Derhaag
Department of Obstetrics and Gynaecology, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
Ellen H. Lambrichs
Department of Genetics and Cell Biology, Clinical Genomics Unit, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
Iris B.W. Boesten
Department of Genetics and Cell Biology, Clinical Genomics Unit, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
Marie Winandy
Laboratory of Organogenesis and Regeneration, GIGA-Research, Univérsité de Liège, 4000 Liège, Belgium
Aafke P.A. van Montfoort
Department of Obstetrics and Gynaecology, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
Katsiaryna Tarbashevich
Institute for Cell Biology, Centre for Molecular Biology of Inflammation, Münster University, 48149 Münster, Germany
Erez Raz
Institute for Cell Biology, Centre for Molecular Biology of Inflammation, Münster University, 48149 Münster, Germany
Mike Gerards
Maastricht Centre for Systems Biology (MaCSBio), Maastricht University Medical Centre, 6200MD, the Netherlands
Jo M. Vanoevelen
Department of Genetics and Cell Biology, Clinical Genomics Unit, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
Bianca J.C. van den Bosch
Department of Genetics and Cell Biology, Clinical Genomics Unit, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
Marc Muller
Laboratory of Organogenesis and Regeneration, GIGA-Research, Univérsité de Liège, 4000 Liège, Belgium
Hubert J.M. Smeets
Department of Genetics and Cell Biology, Clinical Genomics Unit, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Centre, 6200MD Maastricht, the Netherlands
We studied the mtDNA bottleneck in zebrafish to elucidate size, timing, and variation in germline and non-germline cells. Mature zebrafish oocytes contain, on average, 19.0 × 106 mtDNA molecules with high variation between oocytes. During embryogenesis, the mtDNA copy number decreases to ∼170 mtDNA molecules per primordial germ cell (PGC), a number similar to that in mammals, and to ∼50 per non-PGC. These occur at the same developmental stage, implying considerable variation in mtDNA copy number in (non-)PGCs of the same female, dictated by variation in the mature oocyte. The presence of oocytes with low mtDNA numbers, if similar in humans, could explain how (de novo) mutations can reach high mutation loads within a single generation. High mtDNA copy numbers in mature oocytes are established by mtDNA replication during oocyte development. Bottleneck differences between germline and non-germline cells, due to early differentiation of PGCs, may account for different distribution patterns of familial mutations.