The evolutionary importance and affinities of
'amitochondriate' protists

Virginia Edgcomb1, Andrew Roger1,
and Alastair Simpson2
1Woods Hole Oceanographic Institution
2University of Sydney, Australia
Wednesday, November 4, 1998
3:00 p.m.Pacific Forum
It is now widely accepted that the eukaryotes we call protists are far more diverse in
cellular organization than the non-protist eukaryote groupsnamely animals, plants
and fungi. A variety of heterotrophic protists lack classical mitochondria, inhabiting
low- oxygen environments such as the guts and tissues of animals, marine or freshwater
sediments, and the lower reaches of stratified water bodies. Over the last two decades
these 'amitochondriate' organisms have been of great interest to evolutionary biologists,
as some may have diverged before the acquisition of the mitochondrion and consequently
represent very early stages in the evolution of the eukaryotic cell. Some amitochondriate
groupsparticularly the largely parasitic trichomonads, diplomonads, and
microsporidia have indeed tended to form the most basal branches in evolutionary
trees of eukaryotes, based on molecular sequence comparisons. However the validity of
these deep branches has, of late, been vigorously challenged, as has the contention that
these organisms lack any trace of having had mitochondria. To date, almost all of the
research into amitchondriate protists has focused on those groups with parasitic members.
However surveys of sediments and anoxic water bodies reveal a considerable and drastically
understudied diversity of free-living, low-oxygen protists, frequently of unclear
affinities. In several instances, electron-microscopical studies indicate the absence of
classical mitochondria.
Detailed morphological data in concert with molecular phylogenies, covering both
free-living and parasitic taxa, are leading us towards a more authoritative state
regarding the affinities of the amitochondriate protists and whether any groups remain
candidates for being primitively amitochondriate relicts of early eukaryotic evolution.
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