| Autor: |
Peter Buchwald, Fulvia Verde, David J. Wiley, Marbelys Rodriguez Pino, Dimitrios Vavylonis, Illyce Nuñez, Maitreyi Das, Gennaro D'Urso, Chuan Chen |
| Rok vydání: |
2020 |
| Předmět: |
|
| DOI: |
10.1101/2020.06.16.151308 |
| Popis: |
The highly conserved small GTPase Cdc42 regulates polarized cell growth and morphogenesis from yeast to humans. We previously reported that Cdc42 activation exhibits oscillatory dynamics inSchizosaccharomyces pombecells. Mathematical modeling suggests that this dynamic behavior enables a variety of symmetric and asymmetric Cdc42 distributions to coexist in cell populations. For individual wild type cells, however, growth follows a stereotypical pattern where Cdc42 distribution is initially asymmetrical in young daughter cells and becomes more symmetrical as cell volume increases, enabling bipolar growth activation. To explore whether different states of Cdc42 activation are possible in a biological context, we examinedS. pombe rga4Δ mutant cells, lacking the Cdc42 GTPase activating protein (GAP) Rga4. We found that monopolarrga4Δ mother cells divide asymmetrically leading to the emergence of both symmetric and asymmetric Cdc42 distributions inrga4Δ daughter cells. Using genetic screening approaches to identify mutants that alter therga4Δ phenotype, we tested the predictions of different computational models that reproduce the unequal fate of daughter cells. We found experimentally that the unequal distribution of active Cdc42 GTPase in daughter cells is consistent with an unequal inheritance of another Cdc42 GAP, Rga6, in the two daughter cells. Our findings highlight the crucial role of Cdc42 GAP protein localization in determining the morphological fate of cell progeny and ensuring consistent Cdc42 activation and growth patterns across generations. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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