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From Fins to Wings
NOVEMBER 2006

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By Carl Zimmer
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Photographs by Rosamond Purcell
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Scientists are tracing the steps through which evolution forged its successes. They're finding that the same genetic tool kit can build structures both simple and complex.
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The father of evolution was a nervous parent. Few things worried Charles Darwin more than the challenge of explaining how nature's most complex structures, such as the eye, came to be. "The eye to this day gives me a cold shudder," he wrote to a friend in 1860.
Today biologists are beginning to understand the origins of life's complexity—the exquisite optical mechanism of the eye, the masterly engineering of the arm, the architecture of a flower or a feather, the choreography that allows trillions of cells to cooperate in a single organism.
The fundamental answer is clear: In one way or another, all these wonders evolved. "The basic idea of evolution is so elegant, so beautiful, so simple," says Howard Berg, a Harvard researcher who has spent much of the past 40 years studying one of the humbler examples of nature's complexity, the spinning tail of common bacteria. "The idea is simply that you fiddle around and you change something and then you ask, Does it improve my survival or not? And if it doesn't, then those individuals die and that idea goes away. And if it does, then those individuals succeed, and you keep fiddling around, improving. It's an enormously powerful technique."
But nearly 150 years after Darwin first brought this elegant idea to the world's attention when he published The Origin of Species, the evolution of complex structures can still be hard to accept. Most of us can envision natural selection tweaking a simple trait—making an animal furrier, for example, or its neck longer. Yet it's harder to picture evolution producing a new complex organ, complete with all its precisely interlocking parts. Creationists claim that life is so complex that it could not have evolved. They often cite the virtuoso engineering of the bacterial tail, which resembles a tiny electric motor spinning a shaft, to argue that such complexity must be the direct product of "intelligent design" by a superior being.
The vast majority of biologists do not share this belief. Studying how complex structures came to be is one of the most exciting frontiers in evolutionary biology, with clues coming at remarkable speed.
Some have emerged from spectacular fossils that reveal the precursors of complex organs such as limbs or feathers. Others come from laboratories, where scientists are studying the genes that turn featureless embryos into mature organisms. By comparing the genes that build bodies in different species, they've found evidence that structures as seemingly different as the eyes of a fly and a human being actually have a shared heritage.
Scientists still have a long way to go in understanding the evolution of complexity, which isn't surprising since many of life's devices evolved hundreds of millions of years ago. Nevertheless, new discoveries are revealing the steps by which complex structures developed from simple beginnings. Through it all, scientists keep rediscovering a few key rules. One is that a complex structure can evolve through a series of simpler intermediates. Another is that nature is thrifty, modifying old genes for new uses and even reusing the same genes in new ways, to build something more elaborate.
Sean Carroll, a biologist at the University of WisconsinMadison, likens the body-building genes to construction workers. "If you walked past a construction site at 6 p.m. every day, you'd say, Wow, it's a miracle—the building is building itself. But if you sat there all day and saw the workers and the tools, you'd understand how it was put together. We can now see the workers and the machinery. And the same machinery and workers can build any structure."
A limb, a feather, or a flower is a marvel, but not a miracle.
From One Cell to Trillions In every human body roughly ten trillion cells—brainless units of life—come together to work as a unified whole. "It's a complex dance," says Nicole King, a biologist at the University of California, Berkeley, requiring organization and constant communication. And it began more than 600 million years ago when organisms containing just one cell gave rise to the first multicellular animals, the group that now includes creatures as diverse as sea sponges, beetles, and us. It turns out that some of those single-celled ancestors were already equipped for social life.
King studies some of our closest living single-celled relatives, known as choanoflagellates. Choanoflagellates are easy to find. Just scoop some water from a local creek or marsh, put a few drops under a microscope, and you may see the tadpole-shaped creatures flitting about. You can tell them apart from other protozoans by a distinctive collar at the base of their tail.
When King and her colleagues examined the proteins made by choanoflagellates, they found several that were thought to be unique to animals—molecules essential to maintaining a multicellular body. "It really blew our minds," says King. "What are these single-celled organisms doing with these proteins?"
Some of the proteins normally create what King calls "an armlock between cells," keeping animal cells from sticking together randomly. King and her colleagues are running experiments to figure out how choanoflagellates use these adhesive proteins—perhaps to snag bacteria for food. Others play a role in cell-to-cell communication. Choanoflagellates, which presumably have no need to talk to other cells, may use these proteins to sense changes in their environment.
The discoveries suggest that many of the tools necessary to build a multicellular body already existed in our single-celled ancestors. Evolution borrowed those tools for a new task: building bodies of increasing complexity.
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