Frederic D. Bushman
Courtesy of Frederic D. Bushman
The endosymbiotic theory, which posits that organelles such as chloroplasts and mitochondria descended from formerly independent cells, has received wide acceptance in the last third of the 20th century. But recent findings suggest that endosymbiotic processes may have contributed still more cellular components, chloroplasts and mitochondria being simply the most easily identified examples.
Genomic analyses across a broad spectrum of organisms have solidified the case for mitochondria and chloroplasts and suggested that less well known organelles, the hydrogenosome and mitosome, are remnants of genome-depleted mitochondrial descendants. These findings raise questions as to whether still other structures in eukaryotic cells, now lacking their own DNA, might also have originated through endosymbiosis.
THE FEELING IS MUTUAL
According to the presently favored views on endosymbiosis, an anaerobic cell engulfed a respiring α-proteobacterium, allowing respiration in the resulting consortium. This may have taken place during early...
GENES LOST AND FOUND
Mitochondria and chloroplasts differ from bacterial progenitors in that their genomes are greatly reduced, which explains failed attempts at independent cultivation.
Indeed, this gene transfer from organelles to the nucleus is so active that it can readily be measured in the laboratory. Several studies have introduced marker genes into mitochondria and chloroplasts and monitored their rate of appearance in the nuclear genome. Results indicate that the transfer is quite high. And, with an active process it becomes possible to envision a ratchet mechanism for gene swapping. Organellar genes that take care of an overall cellular function can replace their counterparts in the genome as one gene becomes deleted by random mutation.
Similarly, genes needed for organellar function can become transferred to the nuclear genome and incorporated there, provided the encoded protein acquires the signal needed to traffic it back to the organelle. Over eons, the process has reduced the mitochondrial and chloroplast genomes but not completely eradicated them. The same might not be said for other organelles.
... AND LOST AGAIN
Remarkably, two structures appear to have evolved from mitochondria by losing all their DNA, either by deletion or transfer to the nuclear genome. Each of these organelles, the hydrogenosomes and mitosomes, appear in eukaryotic parasites that live in anaerobic environments and no longer need the mitochondria's respiratory functions.456
The hydrogenosome was the first organelle proposed to be a mitochondrial descendent lacking its own genome.4 This organelle, found in some trichomonads, ciliates, and fungi, morphologically resembles mitochondria. Hydrogenosomes are surrounded by a double membrane and participate in energy metabolism, yet they lack a genome, have some differences in membrane architecture, and do not participate in respiration. Instead, hydrogenosomes direct substrate-level phosphorylation, an anaerobic form of energy generation.
Despite these differences, the case for mitochondria as the hydrogenosome's precursor is strong. The genes that encode organelle proteins can be traced to mitochondrial relatives that now reside in the nuclear genome. The encoded proteins traffic back to the organelles, directed by short peptides that resemble mitochondrial trafficking signals. These sequences are functionally interchangeable in the laboratory.
Some organisms, including the anaerobic parasitic amoeba,
The complete sequence of
LIFTING THE LID
Endosymbiosis might have played a larger role in eukaryotic evolution than is currently appreciated. Once you allow that cellular structures lacking their own DNA may indeed be relics of former bacterial mutualists, the lid is off. Margulis and coworkers have proposed that the cellular microtubule network, together with its associated kinetochores and centrioles, might have arisen by capture of a spirochete bacterium.1 In another example, the peroxisome, a membrane-enclosed compartment for specialized oxidative reactions, has been proposed to have arisen from a captured bacterium capable of this chemistry.
But these just scratch the surface with regards to organelle diversity. As the number of complete genome sequences grows, and computational tools become more sensitive, we can investigate proteins in many organelles or subcellular structures for weak genetic signatures of endosymbiotic origin. There still might be some resemblance between microtubule network or peroxisome proteins and genes in modern bacteria. And eukaryotic genes that closely resemble bacterial counterparts might suggest new cellular structures to investigate as potential endosymbiotic products.
A related set of questions surrounds formation of new organelles. Was this process completed eons ago? It seems that gene transfer from mitochondria to the nucleus and stable incorporation into the germ line has largely stopped in metazoan animals, but for other lineages and other organelles it may well be ongoing. In plants, for example, transfer of own genes from the chloroplast to the nucleus appears much more dynamic and potentially continues today.
Looking ahead, we can expect more genome sequences to be determined for partners engaged in mutualistic lifestyles. It should be possible to clarify how often genes are transferred from endosymbionts to their hosts, and analyze this as a function of the intimacy of the mutualistic association. For example, do the mutual interactions seen in
Frederic D. Bushman, professor of microbiology at the University of Pennsylvania School of Medicine, studies the transfer of genetic information between cells and organisms by integrating viruses. He has published more than 80 scientific papers and a book,
He can be contacted at