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Garcia-Pascual, B.

Publications and source records attributed to Garcia-Pascual, B..

2 recordsLinked to original sources

Optimal organelle inheritance strategies under different changing environments and mutational pressures

Mitochondrial and chloroplast DNA (mtDNA and cpDNA) encode essential cellular apparatus. This organelle DNA (oDNA) exists at high copy number (ploidy) in eukaryotic cells, which must both mitigate mutational damage and allow adaptation to changing demands. Across eukaryotes, a range of inheritance strategies are used for oDNA, including uniparental and doubly uniparental inheritance (DUI), paternal leakage, recombination-mediated repair and gene conversion, and an effective "genetic bottleneck" imposed between generations. Here, we use modelling and simulation to investigate how these different strategies support the robustness and evolvability of oDNA populations under different challenges of mutation and changes in selection imposed by the environment. We find a general tradeoff between maintaining heterozygosity for flexible adaptation and supporting purifying selection against dysfunctional mutants. Different combinations of leakage and bottleneck size provide optimal resolutions to this tradeoff under different sets of challenges. The model explains many observed behaviours, including the appearance of non-minimal bottleneck sizes, a tradeoff between high ploidy for heterozygosity and repair and tight bottlenecks for segregation, and environmental dependence of the benefits of leakage and DUI. We connect different strategies observed across eukaryotes with the ecology of the organisms involved to explore support for the predictions of this theory.

evolutionary biology↗

The cellular basis of feeding-dependent body size plasticity in sea anemones

Animals with indeterminate growth can adapt their growth rate and body size to changing food availability throughout their lifetime. As the cellular basis underlying food-dependent growth plasticity is poorly understood, we quantified how the sea anemones Nematostella vectensis and Exaiptasia diaphana (Aiptasia) respond to feeding and starvation on organismal and cellular levels. Using mathematical modelling to analyse growth phases, we found that growth and shrinkage rates in Nematostella are exponential, stereotypic and accompanied by high levels of cell gain or loss, respectively. During starvation and re-feeding, a considerable proportion of juvenile polyp cells (>7%) reversibly shift between S/G2/M and G1/G0 cell cycle phases, suggesting a tight nutritional control of quiescence and cell cycle re-entry. In the facultative symbiotic sea anemone Aiptasia, we found that growth and cell proliferation rates are dependent on the symbiotic state and, in comparison to Nematostella, respond less strongly to changes in food supply. Altogether, we provide a benchmark and resource to study the nutritional regulation of body plasticity on molecular, cellular and genomic levels using the rich functional toolkit available for Nematostella. Summary statementFeeding and starvation in sea anemones induce growth and shrinkage, cell size changes and dynamic cell proliferation changes that support a nutritional control of quiescence and cell cycle re-entry.

developmental biology↗