Evolution of flagella


The evolution of flagella is of great interest to biologists because the three known varieties of flagella each represent a sophisticated cellular structure that requires the interaction of many different systems.

Eukaryotic flagellum

There are two competing groups of models for the evolutionary origin of the eukaryotic flagellum. Recent studies on the microtubule organizing center suggest that the most recent ancestor of all eukaryotes already had a complex flagellar apparatus.

Endogenous, autogenous and direct filiation models

These models argue that cilia developed from pre-existing components of the eukaryotic cytoskeleton as an extension of the mitotic spindle apparatus. The connection can still be seen, first in the various early-branching single-celled eukaryotes that have a microtubule basal body, where microtubules on one end form a spindle-like cone around the nucleus, while microtubules on the other end point away from the cell and form the cilium. A further connection is that the centriole, involved in the formation of the mitotic spindle in many eukaryotes, is homologous to the cilium, and in many cases is the basal body from which the cilium grows.
An apparent intermediate stage between spindle and cilium would be a non-swimming appendage made of microtubules with a selectable function like increasing surface area, helping the protozoan remain suspended in water, increasing the chances of bumping into bacteria to eat, or serving as a stalk attaching the cell to a solid substrate.
Regarding the origin of the individual protein components, a paper on the evolution of dyneins shows that the more complex protein family of ciliary dynein has an apparent ancestor in a simpler cytoplasmic dynein. Long-standing suspicions that tubulin was homologous to FtsZ were confirmed in 1998 by the independent resolution of the 3-dimensional structures of the two proteins.

Symbiotic/endosymbiotic/exogenous models

These models argue that the cilium evolved from a symbiotic Gracilicutes that attached to a primitive eukaryote or archaebacterium.
The modern version of the hypothesis was first proposed by Lynn Margulis. The hypothesis, though very well publicized, was never widely accepted by the experts, in contrast to Margulis' arguments for the symbiotic origin of mitochondria and chloroplasts. Margulis did strongly promote and publish versions of this hypothesis until the end of her life.
One primary point in favor of the symbiotic hypothesis was that there are eukaryotes that use symbiotic spirochetes as their motility organelles.
This is an example of co-option and the flexibility of biological systems, and the proposed homologies that have been reported between cilia and spirochetes have stood up to further scrutiny.
Margulis' hypothesis suggests that an archaea acquired tubulin proteins from a eubacter ancestor of Prosthecobacter.
The homology of tubulin to the bacterial replication and cytoskeletal protein FtsZ was an argument against Margulis, as FtsZ alike protein was apparently found natively in archaea, it was suggesting an endogenous ancestor to tubulin.

Bacterial flagellum

There is good evidence that the bacterial flagellum has evolved from a Type III secretory and transport system, given the similarity of proteins in both systems.
All currently known nonflagellar Type III transport systems serve the function of exporting toxin into eukaryotic cells. Similarly, flagella grow by exporting flagellin through the flagellar machinery. It is hypothesised that the flagellum evolved from the type three secretory system. For example, the bubonic plague bacterium Yersinia pestis has an organelle assembly very similar to a complex flagellum, except that is missing only a few flagellar mechanisms and functions, such as a needle to inject toxins into other cells. The hypothesis that the flagellum evolved from the type three secretory system has been challenged by recent phylogenetic research that strongly suggests the type three secretory system evolved from the flagellum through a series of gene deletions. As such, the type three secretory system supports the hypothesis that the flagellum evolved from a simpler bacterial secretion system.

Eubacterial flagellum

Eubacterial flagellum is a multifunctional organelle. It’s also one of a range of motility systems in bacteria. The structure of the organelle appears like a motor, shaft and a propeller. However, the structure of eubacterial flagellae varies based on whether their motor systems run on protons or sodium, and on the complexity of the flagellar whip. The evolutionary origin of eubacterial flagellae is probably an example of indirect evolution. A hypothesis on the evolutionary pathway of the eubacterial flagellum argues that a secretory system evolved first, based around the SMC rod- and pore-forming complex. This is presumed to be the common ancestor of the type-III secretory system and the flagellar system. Then, an ion pump was introduced to this structure which improved secretion. The ion pump later became the motor protein. This was followed by the emergence of the proto-flagellar filament as part of the protein-secretion structure. Gliding-twitching motility arose at this stage or later and was then refined into swimming motility.

Archaeal flagellum

The recently-elucidated archaeal flagellum, or archaellum, is analogous—but not homologous—to the bacterial one. In addition to no sequence similarity being detected between the genes of the two systems, the archaeal flagellum appears to grow at the base rather than the tip, and is about 15 nanometers in diameter rather than 20. Sequence comparison indicates that the archaeal flagellum is homologous to Type IV pili.. Some Type IV pili can retract. Pilus retraction provides the driving force for a different form of bacterial motility called "twitching" or "social gliding" which allows bacterial cells to crawl along a surface. Thus Type IV pili can, in different bacteria, promote either swimming or crawling. Type IV pili are assembled through the Type II transport system. So far, no species of bacteria is known to use its Type IV pili for both swimming and crawling.

Further research

Testable outlines exist for the origin of each of the three motility systems, and avenues for further research are clear; for prokaryotes, these avenues include the study of secretion systems in free-living, nonvirulent prokaryotes. In eukaryotes, the mechanisms of both mitosis and cilial construction, including the key role of the centriole, need to be much better understood. A detailed survey of the various nonmotile appendages found in eukaryotes is also necessary.
Finally, the study of the origin of all of these systems would benefit greatly from a resolution of the questions surrounding deep phylogeny, as to what are the most deeply branching organisms in each domain, and what are the interrelationships between the domains.