Adaptability and evolution of the cell polarization machinery in budding yeast

Journal Article (2020)
Author(s)

Fridtjof Brauns (LMU Munich)

Leila M. Iñigo de la Cruz (Kavli institute of nanoscience Delft, TU Delft - Applied Sciences)

Werner K.G. Daalman (Kavli institute of nanoscience Delft, TU Delft - Applied Sciences)

Ilse de Bruin (Student TU Delft, Kavli institute of nanoscience Delft)

Jacob Halatek (Microsoft Research Cambridge, LMU Munich)

Liedewij Laan (Kavli institute of nanoscience Delft, TU Delft - Applied Sciences)

Erwin Frey (LMU Munich)

Research Group
BN/Liedewij Laan Lab
DOI related publication
https://doi.org/10.1101/2020.09.09.290510 Final published version
More Info
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Publication Year
2020
Language
English
Research Group
BN/Liedewij Laan Lab
Journal title
bioRxiv
Issue number
1
Volume number
14
Article number
6504
Downloads counter
347
Collections
Institutional Repository
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Abstract

How can a self-organized cellular function evolve, adapt to perturbations, and acquire new sub-functions? To make progress in answering these basic questions of evolutionary cell biology, we analyze, as a concrete example, the cell polarity machinery of Saccharomyces cerevisiae. This cellular module exhibits an intriguing resilience: it remains operational under genetic perturbations and recovers quickly and reproducibly from the deletion of one of its key components. Using a combination of modeling, conceptual theory, and experiments, we propose that multiple, redundant self-organization mechanisms coexist within the protein network underlying cell polarization and are responsible for the module’s resilience and adaptability. Based on our mechanistic understanding of polarity establishment, we hypothesize that scaffold proteins, by introducing new connections in the existing network, can increase the redundancy of mechanisms and thus increase the evolvability of other network components. Moreover, our work gives a perspective on how a complex, redundant cellular module might have evolved from a more rudimental ancestral form.