Evolution of cells: Difference between revisions
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{{see also|Eukaryotes}}, ''[[Archaea]], [[Bacteria]]'' | {{see also|Eukaryotes}}, ''[[Archaea]], [[Bacteria]]'', [[Origin of life]] | ||
<blockquote>"The evolution of modern cells is arguably the most challenging and important problem the field of Biology has ever faced. In Darwin's day the problem could hardly be imagined. For much of the 20th century it was intractable. In any case, the problem lay buried in the catch-all rubric "origin of life"---where, because it is a biological not a (bio)chemical problem, it was effectively ignored. Scientific interest in cellular evolution started to pick up once the universal phylogenetic tree, the framework within which the problem had to be addressed, was determined . But it was not until microbial genomics arrived on the scene that biologists could actually do much about the problem of cellular evolution." ([[Carl Woese]], 2002) <ref> Woese C (2002) [http://www.pnas.org/cgi/content/full/99/13/8742 On the evolution of cells.] ''Proc Natl Acad Sci USA'' '''99''':8742-7 PMID 12077305 This article shifts the emphasis in early [[Phylogenetics|phylogenic adaptation]] from vertical to horizontal gene transfer. (Open access.)</ref></blockquote> | <blockquote>"The evolution of modern cells is arguably the most challenging and important problem the field of Biology has ever faced. In Darwin's day the problem could hardly be imagined. For much of the 20th century it was intractable. In any case, the problem lay buried in the catch-all rubric "origin of life"---where, because it is a biological not a (bio)chemical problem, it was effectively ignored. Scientific interest in cellular evolution started to pick up once the universal phylogenetic tree, the framework within which the problem had to be addressed, was determined . But it was not until microbial genomics arrived on the scene that biologists could actually do much about the problem of cellular evolution." ([[Carl Woese]], 2002) <ref> Woese C (2002) [http://www.pnas.org/cgi/content/full/99/13/8742 On the evolution of cells.] ''Proc Natl Acad Sci USA'' '''99''':8742-7 PMID 12077305 This article shifts the emphasis in early [[Phylogenetics|phylogenic adaptation]] from vertical to horizontal gene transfer. (Open access.)</ref></blockquote> |
Revision as of 17:00, 22 January 2007
- See also: Eukaryotes, Archaea, Bacteria, Origin of life
"The evolution of modern cells is arguably the most challenging and important problem the field of Biology has ever faced. In Darwin's day the problem could hardly be imagined. For much of the 20th century it was intractable. In any case, the problem lay buried in the catch-all rubric "origin of life"---where, because it is a biological not a (bio)chemical problem, it was effectively ignored. Scientific interest in cellular evolution started to pick up once the universal phylogenetic tree, the framework within which the problem had to be addressed, was determined . But it was not until microbial genomics arrived on the scene that biologists could actually do much about the problem of cellular evolution." (Carl Woese, 2002) [1]
An early question that needs to be confronted, indeed a question that in the last analysis requires definition, is: What is life? Most biologists would agree that self-replication, genetic continuity, is a fundamental trait of the life process. Systems that generally would be deemed nonbiological can exhibit a sort of self-replication, however. Examples would be the growth of a crystal lattice or a propagating clay structure. Crystals and clays propagate, unquestionably, but life they are not. There is no locus of genetic continuity, no organism. Such systems do not evolve, do not change in genetic ways to meet new challenges. Consequently, the definition of life should include the capacity for evolution as well as self-replication. Indeed, the mechanism of evolution---natural selection---is a consequence of the necessarily competing drives for self-replication that are manifest in all organisms. The definition based on those processes, then, would be that life is any self-replicating, evolving system (Norman R Pace 2001).[2]
The first cells
The origin of cells was one of the most important steps in evolution of life as we know it. The birth of the cell marked the passage from prebiotic chemistry to biological life. If life is viewed from the point of view of replicator molecules, cells satisfy two fundamental conditions: protection from the outside environment and confinement of biochemical activity. The former condition is needed to keep complex molecules stable in a varying and sometimes aggressive environment; the latter is fundamental for the evolution of biological complexity. If freely-floating molecules that code for enzymes are not enclosed in cells, the enzymes will automatically benefit the neighbouring replicator molecules. This might be viewed as "parasitism by default." Therefore the selection pressure on replicator molecules will be lower, as there is not a definitive advantage for the 'lucky' molecule that produces the better enzyme over the others. If the molecule is enclosed in a cell, then the enzymes coded will be kept close to the replicator molecule itself, and the molecule will benefit from the enzymes it codes for.
Biochemically, cell-like spheroids formed by proteinoids are observed by heating amino acids with phosphoric acid as a catalyst. They bear much of the basic features provided by cell membranes. Proteinoid-based protocells enclosing RNA molecules could (but not necessarily should) have been the first cellular life forms on Earth.
Another theory holds that the turbulent shores of the ancient coastal waters may have served as a mammoth laboratory, aiding in the countless experiments necessary to bring about the first cell. Waves breaking on the shore create a delicate foam composed of bubbles. Winds sweeping across the ocean have a tendency to drive things to shore, much like driftwood collecting on the beach. It is possible that organic molecules were concentrated on the shorelines in much the same way. Shallow coastal waters also tend to be warmer, further concentrating the molecules through evaporation. While bubbles comprised of mostly water tend to burst quickly, oily bubbles happen to be much more stable, lending more time to the particular bubble to perform these crucial experiments. The Phospholipid is a good example of a common oily compound prevalent in the prebiotic seas. Phospholipids can be constructed in ones mind as a hydrophilic head on one end, and a hydrophobic tail on the other. Phospholipids also possess an important characteristic, that is being able to link together to form a bilayer membrane. A lipid monolayer bubble can only contain oil, and is therefore not conducive to harbouring water-soluble organic molecules. On the other hand, a lipid bilayer bubble [1] can contain water, and was a likely precursor to the modern cell membrane. If a protein came along that increased the integrity of its parent bubble, then that bubble had an advantage, and was placed at the top of the natural selection waiting list. Primitive reproduction can be envisioned when the bubbles burst, releasing the results of the experiment into the surrounding medium. Once enough of the 'right stuff' was released into the medium, the development of the first prokaryotes, eukaryotes, and multi-cellular organisms could be achieved. [3]
The eukaryotic cell seems to have evolved from a symbiotic community of prokaryotic cells. It appears that DNA-bearing organelles like mitochondria and chloroplasts are remnants of ancient symbiotic oxygen-breathing bacteria and cyanobacteria, respectively, where the rest of the cell seems to be derived from an ancestral archaean prokaryote cell – a theory termed the endosymbiotic theory. There is still debate about whether organelles like the hydrogenosome predated the origin of mitochondria, or viceversa: see the hydrogen hypothesis for the origin of eukaryotic cells.
How the current lineages of microbes evolved from this postulated community is currently unsolved but subject to intense research by biologists, stimulated by the great flow of new discoveries emerging from genome science.[4]
The common ancestor of eukaryotes, bacteria, and archaea may well have been a community of organisms that readily exchanged components and genes. It would have contained:
- Autotrophs that produced organic compounds from CO2 either photosynthetically or by inorganic chemical reactions;
- Heterotrophs that obtained organics by leakage from other organisms
- Saprotrophs that absorbed nutrients from decaying organisms
- Phagotrophs that were sufficiently complex to envelop and digest particulate nutrients including other organisms
![](/wiki/images/thumb/d/de/Genome_fusion_eukarya.gif/300px-Genome_fusion_eukarya.gif)
Using genomics to infer early lines of evolution
Instead of relying a single gene such as the SSU rRNA gene to reconstruct early evolution, or a few genes, scientific effort has shifted to exploiting the comprehensive information from the many complete genome sequences of organisms that are now available.[5]
It is now clear that trees based only on SSU rRNA alone do not capture the events of early eukaryote evolution accurately, and the origins of the first nucleated cells are still uncertain. For instance, careful analysis of the complete genome of the eukaryote yeast shows that many of its genes are more closely related to bacterial genes than they are to archaea, and it is now clear that archaea were not the simple progenitors of the eukaryotes, in stark contradiction to the findings based on SSU rRNA and limited samples of other genes.[6]
One imaginative but disputed hypothesis getting some support from recent computer-assisted studies of complete genome DNA sequences is that the first nucleated cell arose from two distinctly different ancient prokaryotic (non-nucleated) species that had formed a symbiotic relationship with one-another to carry out different aspects of metablism. One partner of this postulated symbiosis is proposed to be a true bacterial cell, and the other an archaean cell. It is postulated that this symbiotic partnership progressed via the cellular fusion of the partners to generate a chimeric or hybrid cell with a membrane bound internal structure that was the forerunner of the nucleus. The next stage in this scheme was transfer of both partner genomes into the nucleus and their fusion with one-another. Several variations of this hypothesis for the origin of nucleated cells have been suggested[7],
But some biologists dispute this conception[8] and argue for the need for a shift in conceptual framework if this problem is to be solved - and point out that early living communities would compise many different entities to extant cells, and would have shore their genetic material more extensively than current microbes.[9]
References
Citations
- ↑ Woese C (2002) On the evolution of cells. Proc Natl Acad Sci USA 99:8742-7 PMID 12077305 This article shifts the emphasis in early phylogenic adaptation from vertical to horizontal gene transfer. (Open access.)
- ↑ http://www.pnas.org/cgi/content/full/98/3/805 The universal nature of biochemistry
- ↑ This theory is expanded upon in The Cell: Evolution of the First Organism by Joseph Panno
- ↑ Kurland CG et al. (2006) Genomics and the irreducible nature of eukaryote cells. Science 312(5776):1011-4 PMID 16709776
- ↑ Daubin V et al. (2003) Phylogenetics and the cohesion of bacterial genomes. Science 301:829-32 PMID 12907801
- Eisen JA, Fraser CM (2003) Viewpoint phylogenomics: intersection of evolution and genomics. Science 300:1706-7 PMID 12805538
- Henz SR et al. (2005) Whole-genome prokaryotic phylogeny. Bioinformatics 21:2329-35 PMID 15166018
- ↑ Esser C et al. (2004) A genome phylogeny for mitochondria among alpha-proteobacteria and a predominantly eubacterial ancestry of yeast nuclear genes. Mol Biol Evol 21:1643-50 PMID 15155797
- Rivera MC, Lake JA (2004) The ring of life provides evidence for a genome fusion origin of eukaryotes. Nature 431:152-5 PMID 15356622
- Simonson AB et al. (2005) Decoding the genomic tree of life. Proc Natl Acad Sci USA 102 Suppl 1:6608-13 PMID 15851667
- ↑ Esser C et al. (2004) A genome phylogeny for mitochondria among alpha-proteobacteria and a preedominantly eubacterial ancestry of yeast nuclear genes. Mol Biol Evol 21:1643-50 PMID 15155797
- ↑ Kurland CG et al. (2006) Genomics and the irreducible nature of eukaryote cells. Science 312(5776):1011-4 PMID 16709776
- ↑ Woese C (2002) On the evolution of cells. Proc Natl Acad Sci USA 99:8742-7 PMID 12077305
Further reading
- Kurland CG et al. (2006) Genomics and the irreducible nature of eukaryote cells. Science 312(5776):1011-4 PMID 16709776
- Woese C (2002) On the evolution of cells. Proc Natl Acad Sci USA 99:8742-7 PMID 12077305. (Open access.)
- Daubin V et al. (2003) Phylogenetics and the cohesion of bacterial genomes. Science 301:829-32 PMID 12907801
- Eisen JA, Fraser CM (2003) Viewpoint phylogenomics: intersection of evolution and genomics. Science 300:1706-7 PMID 12805538
- Henz SR et al. (2005) Whole-genome prokaryotic phylogeny. Bioinformatics 21:2329-35 PMID 15166018
- Lerat E et al. (2005) Evolutionary origins of genomic repertoires in bacteria. PLoS Biology 3:e130 PMID 15799709
- Steenkamp ET et al. (2006) The protistan origins of animals and fungi. Mol Biol Evol 23:93-106 PMID 16151185]