Does Simple Clumping Explain the Origin of Multicellularity?
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Bergman J.
Author
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D. Budinsky
Author
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M. Nailor
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- Abstract
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Laboratory evolution experiments in which the unicellular green alga Chlamydomonas reinhardtii forms cell clusters under predatory pressure are frequently cited as a direct observation of the origin of multicellularity. We review the most widely discussed of these studies and evaluate the claim against the biological requirements for complex multicellularity and against the predictions of a creation model. The evidence indicates that what was observed is the rapid, heritable expression of a pre-existing capacity for group formation, not the origin of the novel genetic machinery that differentiated multicellular life requires. The evolved clusters remain undifferentiated, lack division of labor, sacrifice motility, and draw on adhesion and extracellular-matrix genes already present in the algal genome and shared with its multicellular relatives. Comparable outcomes in other algae, in yeast, and in bacteria, together with recent work showing that group formation is frequently not adaptive, support the interpretation that these organisms carry engineered, environment-responsive programs for facultative aggregation. We argue that predator-induced clustering is better explained as designed phenotypic plasticity than as a macroevolutionary transition, and we set out the differing predictions of the evolutionary and creation models.
- Author Biographies
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- 2026-07-09
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