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Repurposing of a DNA segregation machinery into a cytoskeletal system controlling cell shape
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Repurposing of a DNA segregation machinery into a cytoskeletal system controlling cell shape

Benjamin L. Springstein, Manjunath G. Javoor, Daniela Megrian +6 more
November 2025
 ·
bioRxiv
 ·
DOI 
10.1101/2025.06.27.661541
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Why this is interesting

This work overturns the assumption that bacterial cytoskeletal functions are fixed by showing that a plasmid segregation system has been repurposed into a shape-controlling cortical cytoskeleton, revealing how multicellularity drives reinvention of fundamental cellular machinery.

Author perspective

What is the most important insight, discovery, or finding from your paper that you would like other scientists to know?
“

Benjamin L. Springstein: A key finding of our study is that bacterial polymer-forming protein systems are remarkably evolutionarily plastic and can be functionally repurposed to support entirely new cellular roles. We show that an ancestral DNA-segregation machinery was co-opted into a novel cytoskeletal system that controls cell shape in multicellular cyanobacteria, an event that coincided with the emergence of cyanobacterial multicellularity. This suggests that the evolution of bacterial multicellularity was accompanied by the acquisition of new structural functions from pre-existing molecular components. More broadly, our work demonstrates that seemingly conserved polymeric protein assemblies can be repeatedly adapted during evolution, implying that many additional examples of such functional innovation remain to be discovered across the tree of life.

Martin Loose: One of the most exciting insights from our paper is seeing evolution in action, not as an inventor, but as a tinkerer.

We found that cells have taken two emergent properties of protein systems that already existed for completely different tasks and repurposed them in a remarkably creative way. The first is dynamic instability: the ability of protein filaments to rapidly grow and collapse. This property is normally used by ParM to form plasmid-segregating filaments to push DNA to opposite ends of a cell before division. In multicellular cyanobacteria, we found that this same filament system, that we renamed to CorMR, has been evolutionarily repurposed to instead control cell shape via a cortical cytoskeleton.

The second is protein oscillations: the Min system, which oscillates from pole to pole in bacteria to mark the cell's midpoint, controlling where FtsZ polymerizes and where division occurs. We discovered that in these cyanobacteria, the Min system has acquired an additional role, it also regulates CorMR polymerization, controlling where these filaments can grow.

What makes this so interesting is that it shows that evolution didn't invent anything new from scratch. Instead, it coopted two pre-existing behaviors, dynamic instability and proteins oscillations, and wired them together for an entirely new purpose: building and maintaining the shape of multicellular cyanobacterial cells. I think this is a beautiful example of evolutionary tinkering, and that the possible functional repertoire of these protein systems is far broader than we previously recognized.

”
Benjamin L. Springstein
&
Martin Loose

QED claims analysis

Summary

In multicellular cyanobacteria, a chromosomally-encoded ParMR system has been functionally repurposed from plasmid DNA segregation into a cortical cytoskeleton (CorMR) that controls cell shape through membrane-associated, antiparallel filaments that are spatially regulated by MinC, representing an evolutionary innovation where CorR acquired membrane-binding capacity via an amphipathic helix while losing DNA-binding function, and MinC gained an extended N-terminal domain enabling competitive inhibition of CorM polymerization.

See full analysis
Main Claim 1 –

Chromosomal ParMR clade in Nostocales/Oscillatoriales has unique features

Supporting evidence

  • CorMR innovations and MinC extensions co-evolved with multicellularity
Main Claim 2 –

Chromosomal ParMR controls cell shape, not DNA segregation

Supporting evidence

  • Cortical CorM filaments transverse; excluded from poles and septa
  • CorM shows in vivo dynamic instability with growth-shrinkage cycles
  • CorR organizes cortical CorM; CorM IDR required for shape
  • CorMR domain deletions phenocopy complete corMR deletion
  • corMR deletion impairs septum maturation and reduces cellular fitness
  • Multiple fluorescent fusions validate cortical CorM/CorR localization
Main Claim 3 –

CorR lacks DNA-binding capacity unlike canonical ParR

Main Claim 4 –

CorR amphipathic helix binds membranes and recruits CorM

Supporting evidence

  • CorR amphipathic helices restricted to multicellular cyanobacteria
  • CorM and CorR activities persist in heterologous E. coli expression
  • CorM-CorR interaction is direct and mediated by CorR helix H5b
  • CorM IDR alters filament properties but not CorR recruitment

Abstract

Bacteria, like eukaryotes, use conserved cytoskeletal systems for intracellular organization. The plasmid-encoded ParMRC system forms actin-like filaments that segregate low-copy plasmids. In multicellular cyanobacteria like Anabaena sp., we found that a chromosomally-encoded ParMR has evolved into a novel cytoskeleton-termed CorMR-with a function in cell shape control rather than DNA segregation. Using live-cell imaging, in vitro reconstitution and Cryo-EM, we demonstrate that CorM forms dynamically unstable, antiparallel double-stranded filaments, which are recruited to the membrane by CorR via an amphipathic helix conserved in multicellular cyanobacteria. CorMR filaments are regulated by MinC, which excludes them from the poles and division plane. Comparative genomics reveal that the repurposing of ParMR and Min systems co-evolved with cyanobacterial multicellularity, highlighting the evolutionary plasticity of cytoskeletal systems in bacteria.

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