This is big idea in the history of evolution. The jump from the lowly bacterium to the cells used to produce complex life was an industrial revolution driven by the advent of mitochondria which is the engine providing the power. The big idea is the recognition that this power plant was central to it all rather say than the nucleus which has been the general assumption.
The emergence of mitochondria turns out to be critical and possibly difficult or perhaps naturally unique inasmuch as it appears to have been made once. It strongly hints that we need to understand it far better because it appears that the rest of the cell can be assembled in many different ways after that with no problems.
In fact this suggests that the panspermia idea may have also been travelling mitochondria.
Energy Revolution Key To Complex Life
by Staff Writers
Image: The Beginning of a Self by Odra Noel
The evolution of complex life is strictly dependent on mitochondria, the tiny power stations found in all complex cells, according to a new study by
"The underlying principles are universal. Energy is vital, even in the realm of evolutionary inventions," said Dr Lane, UCL Department of Genetics, Evolution and Environment. "Even aliens will need mitochondria."
For 70 years scientists have reasoned that evolution of nucleus was the key to complex life. Now, in work published this week in Nature, Lane and Martin reveal that in fact mitochondria were fundamental to the development of complex innovations like the nucleus because of their function as power stations in the cell.
"This overturns the traditional view that the jump to complex 'eukaryotic' cells simply required the right kinds of mutations. It actually required a kind of industrial revolution in terms of energy production," explained Dr Lane.
At the level of our cells, humans have far more in common with mushrooms, magnolias and marigolds than we do with bacteria. The reason is that complex cells like those of plants, animals and fungi have specialized compartments including an information centre, the nucleus, and power stations - mitochondria.
These compartmentalised cells are called 'eukaryotic', and they all share a common ancestor that arose just once in four billion years of evolution.
Scientists now know that this common ancestor, 'the first eukaryote', was a lot more sophisticated than any known bacterium. It had thousands more genes and proteins than any bacterium, despite sharing other features, like the genetic code. But what enabled eukaryotes to accumulate all these extra genes and proteins? And why don't bacteria bother?
By focusing on the energy available per gene, Lane and Martin showed that an average eukaryotic cell can support an astonishing 200,000 times more genes than bacteria.
"This gives eukaryotes the genetic raw material that enables them to accumulate new genes, big gene families and regulatory systems on a scale that is totally unaffordable to bacteria," said Dr Lane. "It's the basis of complexity, even if it's not always used."
"Bacteria are at the bottom of a deep chasm in the energy landscape, and they never found a way out," explained Dr Martin. "Mitochondria give eukaryotes four or five orders of magnitude more energy per gene, and that enabled them to tunnel straight through the walls of the chasm."
The authors went on to address a second question: why can't bacteria just compartmentalise themselves to gain all the advantages of having mitochondria? They often made a start but never got very far.
The answer lies in the tiny mitochondrial genome. These genes are needed for cell respiration, and without them eukaryotic cells die. If cells get bigger and more energetic, they need more copies of these mitochondrial genes to stay alive.
Bacteria face exactly the same problem. They can deal with it by making thousands of copies of their entire genome - as many as 600,000 copies in the case of giant bacterial cells like Epulopiscium, an extreme case that lives only in the unusual guts of surgeonfish.
But all this DNA has a big energetic cost that cripples even giant bacteria - stopping them from turning into more complex eukaryotes. "The only way out", said Dr Lane, "is if one cell somehow gets inside another one - an endosymbiosis."
Cells compete among themselves. When living inside other cells they tend to cut corners, relying on their host cell wherever possible. Over evolutionary time, they lose unnecessary genes and become streamlined, ultimately leaving them with a tiny fraction of the genes they started out with: only the ones they really need.
The key to complexity is that these few remaining genes weigh almost nothing. Calculate the energy needed to support a normal bacterial genome in thousands of copies and the cost is prohibitive. Do it for the tiny mitochondrial genome and the cost is easily affordable, as shown in the Nature paper.
The difference is the amount of DNA that could be supported in the nucleus, not as repetitive copies of the same old genes, but as the raw material for new evolution.
"If evolution works like a tinkerer, evolution with mitochondria works like a corps of engineers," said Dr Martin.\
The trouble is that, while cells within cells are common in eukaryotes, which often engulf other cells, they're vanishingly rare in more rigid bacteria. And that, Lane and Martin conclude, may well explain why complex life - eukaryotes - only evolved once in all of Earth's history.
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