《自然》今天发表了一篇很有意思的短评“独角兽如何长出角的？”。 很多对进化论的怀疑，从一种生物特性发展出另一种生物特性，比如飞行，开花和感知磁场，这是不可思议的神奇。密西根州立大学的Richard Lenski构思从简单生物来验证生物进化的原则：“通过基因复制（copy number）和重组（rewiring）产生新的性状”。这个实验整整做个25年，至今仍在继续。从1988年2月24日，基因完全相同的12个E. coli种群开始培养并繁衍，每天将一定数目的菌群放入液氮冷藏，目前已经繁衍了五万五千代。当新的生物特性出现以后，可以从 液氮中取出若干代父代，以求重现。今天发表的文章用这一方法，分析了E. Coli一种新性状的基因生成机制，明明白白的告诉你 “独角兽如何长出角的？” Evolution: How the unicorn got its horn Heather Hendrickson Paul B. Rainey AffiliationsCorresponding author Nature (2012) doi:10.1038/nature11487 Published online 19 September 2012 An experiment studying bacterial populations over thousands of generations shows that a novel trait can evolve through rearrangement and amplification of a few pre-existing genes. Evolutionary novelties such as flight, flowers and eyes are central to life's diversity, and yet explanations for their origins are anything but straightforward. The difficulty arises because the relevant events happened a long time ago under circumstances that are poorly understood. However, in a paper published on Nature's website today, Blount et al.1 unravel molecular details underpinning a major innovation in a trait (phenotype) that evolved in bacterial populations after 30,000 generations. The capacity to store ancestral types in a state of suspended animation and then sequence their genomes has provided a remarkably complete picture of the main genetic events that gave rise to an instance of evolutionary novelty. The 'modern evolutionary synthesis', which provides the accepted account of evolution, unites Charles Darwin's gradualism — the view that evolution proceeds through gradual changes — with Gregor Mendel's concept of genes as discrete units. But some have argued that the resulting notion of incremental mutational change does not provide an adequate framework for explaining how phenotypic innovations arise2, 3. What steps precede a major evolutionary advance such as the eye? Far from being a simple philosophical point, the need for mechanistic understanding at this level is paramount, and Blount et al. (researchers in Richard Lenski's laboratory) provide direct insight into how innovation happens. In 1988, Lenski initiated what is now the longest-running project in experimental evolution. He took a clone (a group of genetically identical cells derived from a single cell) of the fast-growing bacterium Escherichia coli and founded 12 independent populations, each resident in a flask containing a simple medium, with glucose as the sole source of carbon. Every day for almost 25 years, a sample of each population has been transferred to a fresh flask — which means that these populations have gone through 55,000 generations. In addition to daily transfer, the researchers have been periodically storing samples at −80 °C, thereby ensuring access to a detailed history of ancestral states. Moreover, unlike fossils, these frozen ancestors are readily brought back to life. Although Lenski's group reported adaptations that improved the microbes' fitness from the earliest stages of the experiment, something remarkable happened after about 31,000 generations. One of the populations (Ara-3) evolved the capacity to use citrate as a nutrient4. Citrate, a chelating agent that facilitates iron uptake, is a component of the growth medium. Although E. coli can 'digest' citrate when oxygen is absent, it typically cannot do so under the aerobic conditions of this experiment. The fact that the microbe can use citrate under some circumstances raises an important point: new genes are not invented de novo. Quite the contrary — evolution builds on the raw material at its disposal. The bacterium has the building blocks necessary for the evolution of aerobic citrate utilization, but realization of this capacity requires a rewiring and refinement of regulatory connectivities. To understand the nature of the genetic changes conferring the ability to use citrate in the presence of oxygen (a trait dubbed the Cit+ phenotype), Blount et al. returned to the freezer and resuscitated ancestral Cit− populations from earlier time points in the Ara-3 lineage. When the researchers tried to 'replay' the evolution of the trait, they found that the Cit+ phenotype appeared again only in populations derived from the most recent Cit− lineages. This result suggested that genetic changes had occurred in these lineages that made it possible for the Cit+ phenotype to evolve. Although the precise nature of such 'potentiating' mutations is unclear, the important fact is that they took place (Fig. 1). Figure 1: The evolution of a new trait. In 1988, Richard Lenski took a single clone formed by genetically identical Escherichia coli bacteria and propagated it, with daily transfer, in 12 independent flasks. Whereas the original cells could use citrate as a nutrient only in the absence of oxygen (Cit− cells), bacteria in one of the flasks eventually evolved the ability to use it with oxygen present (Cit+ cells, indicated in red). After analysing the genomes of the microbes at different stages of the process, Blount et al.1 (researchers in Lenski's laboratory) found that the original clone had diverged into competing lineages — some of which went extinct and some of which prospered. The authors report that, for the new ability to appear, the bacterial populations went through three successive evolutionary steps. 'Potentiating' mutations (of unclear nature) were required for cells to acquire 'actualizing' mutations that consisted of a specific rearrangement of a few genes and that allowed some growth — although poor — on citrate in the presence of oxygen. Further 'refining' mutations, which involved duplications of the rearranged DNA sequence, were needed for robust growth under such conditions. Full size image (37 KB) The step that made the cells weakly Cit+ — the 'actualization' step — was easier to identify. The authors examined a genomic region that carries the gene citT, which encodes a protein (citrate transporter) needed for citrate to enter the cell. In the original bacterial strain, citT is located downstream of citG (another gene required for citrate utilization) and rnk, a functionally unrelated gene that participates in energy metabolism. In each of the derived Cit+ cells, Blount et al. found a distinctive genomic rearrangement that fused rnk to citG. As a result, expression of citG and citT came under the control of the promoter (regulatory sequence) of rnk, which allowed their expression in the presence of oxygen. What's more, the authors found that a single copy of the genetic rearrangement was insufficient to generate the Cit+ phenotype, and that there was a tandem array of between two and nine copies in Cit+ cells. Therefore, gene duplications took a very low level of citrate transport and propelled it to life-sustaining levels. All cells that inherited the genetic fusion (the actualizing mutation), followed by amplification (a 'refining' mutation), were Cit+. The discovery of the Cit+ mutants in Lenski's experiment has been a mote in the eye for those suggesting that major phenotypic innovations cannot be explained by microevolutionary (gradual) processes. Indeed, for anti-evolutionists, lack of mechanistic detail has even allowed room for divine intervention. After several attempts to politely address the concerns of one critic, Lenski responded publicly in what has proven to be one of the most competent and direct defences of science versus dogma for some time. It includes the memorable phrase5, “In other words, it's not that we claim to have glimpsed 'a unicorn in the garden' — we have a whole population of them living in my lab!”. With knowledge of the key events that determine this unicorn's horn, one can next look for lessons of a general nature. The idea that genetic evolution might conform to a set of rules is attractive6. Capture and amplification of other genes' promoters have been shown to facilitate adaptation in a variety of situations7, 8, but the extent to which these kinds of events can fuel phenotypic innovation depends on prior history, chance and fortuitous factors such as genome architecture. Blount and colleagues' work shows that evolution, given sufficient time, will take advantage of any opportunity — but opportunity may depend on the most fickle of potentiating events. Unfortunately, predicting the nature of these crucial potentiating mutations may well lie beyond reach. Nevertheless, on a positive note, this work strengthens a central premise of the modern evolutionary synthesis: genetic change is gradual. Phenotypic change, however, can be dramatic. References References Author information Blount, Z. D., Barrick, J. E., Davidson, C. J. Lenski, R. E. Nature http://dx.doi.org/10.1038/nature11514 (2012). Show context Pigliucci, M. Phil. Sci. 75, 887–898 (2008). Show context Gould, S. J. The Structure of Evolutionary Theory (Belknap, 2002). Show context Blount, Z. D., Borland, C. Z. Lenski, R. E. Proc. Natl Acad. Sci. USA 105, 7899–7906 (2008). PubMed Article Show context http://rationalwiki.org/wiki/Lenski_affair Show context Stern, D. L. Orgogozo, V. Science 323, 746–751 (2009). CAS ISI PubMed Article Show context Whoriskey, S. K., Nghiem, V. H., Leong, P. M., Masson, J. M. Miller, J. H. Genes Dev. 1, 227–237 (1987). CAS ISI PubMed Article Show context Andersson, D. I. Science 282, 1133–1135 (1998). CAS ISI PubMed Article Show context Download references Author information References Author information Affiliations Heather Hendrickson and Paul B. Rainey are at the New Zealand Institute for Advanced Study, Massey University, Auckland, 0745, Massachusetts, New Zealand. P.B.R. is also at the Max Planck Institute for Evolutionary Biology, plön, Germany Paul B. Rainey Corresponding author Correspondence to: Paul B. Rainey
标签: 生物进化
