Constraints on the G1/S transition pathway may favor selection of simple multicellularity as a passenger phenotype
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Multicellularity is present throughout the entire tree of life. While the formation of simple multicellular entities can result from aggregation of cells or clonal development, it is not yet fully understood how, once formed, these simple multicellular entities could be maintained or even selected for. Here, using the yeast mutant ace2 snowflake as a model of simple multicellularity, we aimed at identifying genetic conditions favoring its maintenance. Growth-competition experiments revealed that, while the ace2 mutation by itself does not provide any advantage or disadvantage, the ace2 snowflakes were strongly selected when combined to conditions affecting regulators of the G1/S transition of the cell cycle, such as Cln3 or Whi5. We show that this selection results from a faster exit from stationary phase of the ace2 snowflake. Importantly, this advantage is not dependent on the multicellular phenotype, but rather on the ace2 genotype itself. We found that the ace2 selective advantage in the cln3 background fully depends on the KSS1 gene, another target of the Ace2 transcription factor. Finally, we show that results similar to those obtained with ace2 mutants are phenocopied by the AMN1 368D allelic form found in all feral yeast strains, hence bringing a strong physiological relevance to these observations. Altogether, our results support the hypothesis that simple multicellularity could persist, not because it provides a direct selective advantage due to multicellularity itself, but rather as a passenger phenotype that is maintained alongside other selected traits.
SIGNIFICANCE
While appearance of simple multicellularity does not seem so rare during evolution, what drove its maintenance and kept these simple multicellular entities away from counter-selection long enough for them to evolve sophisticated modes of cooperation such as division of labor, is questioning. A simple type of explanations is that multicellularity by itself could be advantageous, for example by allowing to escape predation or favoring resistance to stresses. Here we show that, alternatively, multicellularity can be selected as a phenotypic passenger of a mutation that is selected for another reason i.e. regulation of cell cycle progression. This initial absence of selective pressure on multicellularity itself may offer favorable conditions for further evolution.
