Scientists have discovered a novel genetic repair process that allows a hardy desert microbe to die and resurrect itself over and over again.
The finding, detailed in the Sept. 28 issue of the journal Nature, could lead to new forms of regenerative medicines and might even allow scientists to one day bring dead cells in our own bodies back to life.
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Without a genome, the microbe is effectively dead because it can't synthesize the proteins necessary for life.
In only a few hours, though, Deinococcus can reassemble its genome and return to life.
"This is the first case, I think, of a living cell that clinically dies — its DNA is chopped into little pieces and it has no metabolism — when desiccated, and yet, as long as it can reconstitute its genome, it reconstitutes its own life," said study team member Miroslav Radman of the University of Paris.
The microbe is able to perform its remarkable feat because, like other bacteria, it carries at least two, sometimes more, copies of its genome and also because radiation damages DNA randomly.
So even if both genome copies are damaged, they likely aren't damaged in the same spots.
With the right tools, a microbe can piece together what the original sequence was.
Returning to life
Here's how it works: When it Deinococcus' genome initially shatters, it breaks apart into numerous double-stranded DNA fragments.
Proteins chew away at the ends of the fragments, creating overhanging single-stranded DNA "tails."
The tails are called "sticky-ends" because they can combine with each other.
To function, the sticky-ends have to contain complementary DNA sequences.
DNA is made up of four amino-acid bases, or "letters," that combine in specific ways: adenine (A) always pairs with thymine (T) and guanine (G) with cytosine (C).
So if the sequence on one tail is ATG, it can pair with another tail whose sequence is TAC. Two complimentary sticky ends will fit together naturally like toy Lego blocks.
The sticky-ends allow sequential DNA fragments to be joined together to form linear, double-stranded intermediate pieces.
A protein then arranges the double-stranded pieces into circular chromosomes, which are characteristic of bacteria.
"Once the genome is reconstituted, the cell can synthesize [again] all of its proteins, lipids and membranes and the cell resurrects," Radman said.
Potential human applications
Although the basic mechanism behind Deinococcus' hardiness is understood, many mysteries still remain.
For one, proteins are needed for DNA repair and synthesis, but proteins can be damaged by radiation, too.
It's one thing to piece together a broken genome, but how does Deinococcus do it with broken tools?
"That's still a mystery," Radman told LiveScience. "How, after months of desiccation and burning from UV sunlight in the desert, is there still sufficient protein activity to start reconstituting DNA? We don't know."
One possibility is that Deinococcus' proteins are resistant to dehydration, in the same way proteins in thermophilic bacteria are resistant to temperature.
Radman believes his team's findings open up the possibility of resurrecting dead cells in our own bodies, specifically those in our brains.
"It allows us now, legitimately, to dream of bringing back to life dead, or close-to-dead, neurons," he said.
Unlike most bacteria studied in biology, such as E. coli and salmonella, Deinococcus is a slow grower. It didn't evolve to divide rapidly, but to be robust.
"It sort of went the other way of capitalism — it doesn't care about growth and fast division because it doesn't need to compete in the desert with anybody," Radman said. "So in that sense, Deinococcus is the bacterial paradigm of neurons, which [usually] don't divide during our lifetimes."
Like Deinococcus, neurons carry two — albeit slightly different — copies of their genomes: one from Mom and the other from Dad.
In fact, all the cells in our bodies, except sperm and eggs, contain two genome copies.
Therefore, it's possible that one day scientists could resurrect dead neurons using repair mechanisms similar to those employed by Deinococcus, Radman said.
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