ࡱ> vxu =bjbj,, $zNN5mmmmm &|||)8m||||mmmm|:,mmlR:. 08Rm||| 3:   The Search for LUCA Natural History Nov. 2000 Did the Last Universal Common Ancestor look like a bacterium--or like one of your own cells? By Matt Ridley What was the first organism with DNA like? Scientists have traditionally assumed it was some kind of primitive bacterium. But recent research suggests that the long-looked-for "it" may have been more of a "them." And according to a controversial new theory, the first organisms equipped with DNA may have resembled one of our own cells more closely than they resembled bacteria. All living creatures--be they amoebas, beech trees, beetles, or bacteria--share a common ancestor that lived about 4 billion years ago. We infer the existence of this Last Universal Common Ancestor--or LUCA--from the many features shared by all organisms, most notably the unique code that translates the language of DNA into the language of proteins, the things that actually do all the work inside cells. If there were other, rival life-forms here on Earth, they died out long ago. By comparing the similarities and differences in the genes of different organisms, we can climb down the family tree and observe where it branches. Take our own lineage. Five million years ago, the Homo sapiens branch meets that of chimpanzees; a few million years before that, the common ancestor of humans and chimps merges with gorillas; and so on, back to the first mammal, the first reptile, the first vertebrate, the first multicellular animal. Finally we get to the common ancestor of all animals, plants, protists, and fungi. This undoubtedly tiny organism was the last common ancestor of all present-day eukaryotes (organisms possessing cells with a nucleus). At this juncture, scientists long thought, there was only one convergence left: between eukaryotes and prokaryotes (single celled organisms with no nucleus). For most of the twentieth century, prokaryotes had generally been considered synonymous with bacteria. But in 1977 Carl Woese, of the University of Illinois, found a fundamental division within the prokaryotes: between bacteria and what he called archaea, a diverse group of cells that look very like bacteria but differ genetically and are often found in extremely hot environments, such as hot springs, with temperatures above 203 [degrees] F. Woese totted up the genetic differences between the two kinds of prokaryotes and concluded that the trifurcation of life--into eukaryotes, bacteria, and archaea--must have occurred more than 3 billion years ago. But which of the three groups appeared first? Are we eukaryotes more closely related to bacteria or to archaea? To find out, researchers in the mid-1980s turned to the enzyme RNA polymerase and other factors involved in the synthesis of proteins, some of the most ancient and universal pieces of machinery in the cell. After comparing these proteins in species from the three groups of organisms, the scientists concluded that plants, animals, and fungi are more closely related to archaea than to bacteria. Comparisons of other proteins, however, contradicted this conclusion: some suggested that eukaryotes and bacteria were closer kin, while still others suggested that archaea and bacteria were. By the mid-1990s, the situation had become a mess. The only explanation for these contradictory patterns, according to W. Ford Doolittle, of Dalhousie University in Nova Scotia, is to assume that at some point in the early history of life, there was promiscuous sharing of genes among species--or even mergers of whole organisms. Woese agrees. He now thinks that "the Last Universal Common Ancestor was not a discrete entity but rather a diverse community of cells that evolved as a biological unit." There the matter might have rested but for a meeting convened in 1996 at Les Treilles, near Paris, to discuss the confusing tree of life. Attending that meeting was Patrick Forterre, a scientist from the Universite Paris-Sud. Forterre had a heretical view. He challenged the generally accepted idea that bacteria (or archaea) predated all other creatures on Earth. He even doubted that they were primitive. The long-standing "prokaryote dogma," he claimed, was based on the prejudice that the simple must precede the complex. His own work on a bacterial enzyme called DNA gyrase had convinced him that bacteria are actually quite advanced. Gyrase is a powerful and sophisticated tool--and it's a tool eukaryotes do not possess. The more Forterre considered the streamlined simplicity and effectiveness of a bacterial cell, the more he was convinced that the clunky machinery in eukaryotic cells represented an older, more primitive technology. Forterre and his colleague Herve Philippe have now gathered many examples that support their case. Take RNA polymerase. This enzyme creates working copies of DNA (called messengers) used in gene translation. The version we eukaryotes use has up to thirteen components, each made by a separate gene. In addition, it is assisted by twenty or so "transcription factors," by a ten-part "spliceosome" (a machine whose job it is to cut out the pieces of nonmessage text, called introns, that interrupt eukaryotic genes), and by a six-part "polyadenylation device." The RNA polymerase used by archaea also has a large number of components (eight to twelve) and is assisted by only two or three other genes. The truly striking contrast, however, appears in the version used by bacteria, which has just three components and a single assistant. The traditional view would be that the complications found in eukaryotic RNA polymerase were added over the eons. But it could just as easily have happened the other way round, with bacteria slimming down the RNA polymerase machinery to its most efficient form. In plants, animals, and fungi, the synthesizing, capping, splicing, polyadenylating, and transporting of a DNA messenger takes about thirty minutes. In bacteria, the process is completed in a matter of seconds. Forterre argues that his scenario of moving from a complex eukaryotelike common ancestor to a simpler but more efficient prokaryotic system is more appealing than the classical hypothesis that views prokaryotes as the more primitive organisms. Appealing, maybe--but how strong a case can be made for his idea? There is no question that simplification does occur during evolution. Over time, parasitic lineages lose sense organs and brains they do not need. Microsporidia are a good example. These pathogens were once thought to be a missing link between primitive prokaryotes and advanced eukaryotes because they are so simple and because they lack mitochondria. We now know that microsporidia are nothing so special--they're merely cousins of fungi that have become drastically simplified by their parasitic life. Likewise, many biologists are convinced that viruses, which borrow the biochemistry of their hosts to reproduce themselves, are not derived from primitive independent life-forms but are little packets of rogue genes that have escaped from higher organisms. If viruses are reduced organisms, then why couldn't bacteria be as well? The eukaryotic cell is stuffed full of features that have no counterpart in bacteria or archaea and that, Forterre argues, no self-respecting life-form would invent unless it absolutely had to. We eukaryotes have telomeres, for example: specially constructed caps of DNA on the ends of chromosomes that prevent the tips from fraying. (Fraying is now thought to be one of the chief symptoms of aging.) But telomeres are unnecessary in bacteria, which have circular chromosomes and thus no ends to fray. And then there are our spliceosomes: bacteria have no introns and thus no need for spliceosomes. The most convincing part of Forterre's case is an argument developed by three New Zealanders: Anthony Poole, Daniel Jeffares, and David Penny, all at Massey University. They point out that a great many of the special features of eukaryotes have working components made of molecules of RNA, which is almost universally regarded as the primitive precursor of DNA. Telomerase, the enzyme that repairs telomeres, has working RNA inside it. So does the spliceosome. And RNA is crucial to the synthesis of proteins. The presence in eukaryotic cells of these working machines made from a more ancient material suggests to Forterre and his like-minded colleagues that they are relics of an earlier age. Moreover, RNA has a property that DNA lacks almost entirely--it can act as a catalyst to assist chemical reactions. Most current hypotheses about the history of life before LUCA envisage an entire RNA world of "riboorganisms," with RNA genes and RNA enzymes. Only later, according to these hypotheses, did some fortunate descendant invent both the much subtler catalytic machinery of protein and the much more chemically stable information-storage device called DNA. At that point, RNA was demoted to being the link between DNA and proteins. If the scenario of an ancestral RNA world is correct, then why, Forterre asks, do eukaryotes have much more complicated RNA machinery in their cells than bacteria and archaea do? And if, as Poole and his colleagues say, all these RNA devices are indeed molecular "living fossils" left over from a different world, then it seems unlikely that eukaryotes would have invented all this machinery to complicate their lives and used an old technology to do so. That would be a bit like finding wooden parts working in the innards of a computer. Additional support for the idea that eukaryotes evolved before prokaryotes can be seen in the structure of their chromosomes. Each chromosome is a very long molecule of DNA. We humans have twenty-three pairs of them--forty-six separate DNA molecules. Other species of eukaryote have different numbers of paired DNA molecules, but in all of us, the molecules come in separate chromosomes. Compare this with the single, circular chromosome of bacteria and archaea. Now imagine one system evolving from the other. If the prokaryotic system came first, the eukaryotes would have had to chop the ancestral chromosome into sections, add telomeres to their ends, and drop the equipment that closes the circle. If, however, the eukaryotic system arose earlier, the machinery for making a single circular chromosome would already have been in place: a single enzyme called reverse transcriptase. This enzyme makes a circular DNA copy of an RNA transcript (after the introns have been edited out by the spliceosome). Multiple copies of reverse transcriptase are present in all genomes, having been left there by retroviruses containing genes for the enzyme. The Forterre-Poole hypothesis envisages that some primitive retrovirus left behind a reverse transcriptase gene in a proto-eukaryotic organism, which used it by chance, one day, to make a circular chromosome. And separate linear chromosomes may not be the only primitive feature of our genome: the very habit of using pairs of chromosomes, one from each parent, may also be a relic from the days when transcription errors were more common and spare copies would thus have come in handy. If Forterre and Poole are right about eukaryotes being the steam engines of the living world, then how did we manage to remain so successful? The answer may lie in several features of modern eukaryotic cells that bacteria have not invented--in particular, the ability to engulf other cells. This talent allows some protozoa (single-celled eukaryotes) to pursue a largely predatory way of life. It is also the source of our immune system's ability to consume or otherwise incorporate invading bacteria and sometimes to benefit by their presence. Some bacteria engulfed in this way went on to become mitochondria, symbionts living inside the eukaryotic cell and providing it with energy. In addition, the eventual evolution of multicellularity in eukaryotes brought the immense advantages that accompany division of labor in a large body and helped offset the biochemical disadvantages of poorly developed genetic machinery. As with most attempts to reconstruct the history of life, Forterre's argument for a eukaryotic LUCA would be greatly strengthened by fossil evidence. The oldest known fossils are the 3.5-billion-year-old stromatolites discovered in western Australia in 1980. These small, pillow-shaped structures were almost certainly laid down by living organisms, but it is difficult to determine for certain what kind of creature built them. Modern stromatolites are usually--but not always--made by bona fide prokaryotes, and the common assumption is that the ancient ones were, too. But there is no hard evidence for this. And last year Jochen Brocks and his colleagues at the Australian Geological Survey Organisation made a remarkable discovery. They extracted hydrocarbon from 2.7-billion-year-old shales in the form of bitumen and subjected it to spectrographic analysis to see what it was made of. They were surprised to find a group of compounds called steranes--hydrocarbons made by eukaryotes but not by prokaryotes. The result, they say, provides persuasive evidence for the existence of eukaryotes 500 million to 1 billion years before the fossil record currently indicates that the lineage arose. In other words, the "age of prokaryotes," which all the textbooks say preceded the age of eukaryotes, might never have existed. Forterre's theory has by no means won the field. But he has done a great service by pointing out what a naked emperor the prokaryotic dogma may turn out to be. Matt Ridley is the author of Genome: The Autobiography of a Species in 23 Chapters, an adaptation of which appeared in the March issue of Natural History. COPYRIGHT 2000 Natural History Magazine, Inc. 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