White Collar Proteins Help Fungi Do It in the Dark

Average earth temperatures rose 0.6 ºC over the last century, according to the latest Intergovernmental Panel on Climate Change. But that increase pales in comparison to the 1.4–5.8 ºC expected increase over this century. As temperatures climb, climate models predict that high-latitude, high-altitude regions like Yellowstone National Park will experience shorter winters and earlier snow melts. How these environmental shifts will impact species and ecosystems remains to be seen. The effects of climate change are already evident at the species level, with disruptions in range, reproductive success, and seasonal phenomena like migration, and the decoupling of evolutionarily paired events like new births and food availability. Both experimental and data-driven modeling studies predict that climate change may well precipitate shifts in the structure of ecosystems as well. In a new study, Christopher Wilmers and Wayne Getz investigated the effects of climate change on ecosystem dynamics by studying a keystone species in Yellowstone, the gray wolf (Canis lupus). Gray wolves inhabited most of North America until US extirpation campaigns nearly eradicated them by the 1930s. In 1995, the US Fish and Wildlife Service reintroduced the persecuted predator into Yellowstone. Wilmers and Getz used data from the past 50 years at two weather stations in the park's northern range (where elk over winter and four to six wolf packs now A standard evolutionary assumption is that the DNA of closely related species should be more similar in both structure and function than that of more distantly related ones. This parsimonious rule of thumb holds true across wide expanses of time and among widely divergent species, but it has exceptions. In this issue, Michael Ludwig and colleagues show that one exception is in an enhancer region of a key developmental gene in fruitfl ies of the genus Drosophila. Here, the enhancer is functionally similar enough in two species that diverged 60 million years ago that switching them produces normal development, but different enough in two species separated by only 10 million years that exchanging them between the two fl ies aborts development. The gene in question is even-skipped, a patterning gene that creates seven transverse stripes along the anterior– posterior axis in the fruitfl y embryo. Its expression is regulated by fi ve enhancing elements located upstream from the promoter. The best characterized of these, the stripe 2 enhancer (S2E), binds fi ve different transcription factors at multiple locations. Ludwig et al. deleted S2E …


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Average earth temperatures rose 0.6 ºC over the last century, according to the latest Intergovernmental Panel on Climate Change. But that increase pales in comparison to the 1.4-5.8 ºC expected increase over this century. As temperatures climb, climate models predict that high-latitude, high-altitude regions like Yellowstone National Park will experience shorter winters and earlier snow melts. How these environmental shifts will impact species and ecosystems remains to be seen.
The effects of climate change are already evident at the species level, with disruptions in range, reproductive success, and seasonal phenomena like migration, and the decoupling of evolutionarily paired events like new births and food availability. Both experimental and data-driven modeling studies predict that climate change may well precipitate shifts in the structure of ecosystems as well.
In a new study, Christopher Wilmers and Wayne Getz investigated the effects of climate change on ecosystem dynamics by studying a keystone species in Yellowstone, the gray wolf (Canis lupus). Gray wolves inhabited most of North America until US extirpation campaigns nearly eradicated them by the 1930s. In 1995, the US Fish and Wildlife Service reintroduced the persecuted predator into Yellowstone.
Wilmers and Getz used data from the past 50 years at two weather stations in the park's northern range (where elk over winter and four to six wolf packs now Gray Wolves Help Scavengers Ride Out Climate Change DOI: 10.1371/journal.pbio.0030132 A standard evolutionary assumption is that the DNA of closely related species should be more similar in both structure and function than that of more distantly related ones. This parsimonious rule of thumb holds true across wide expanses of time and among widely divergent species, but it has exceptions. In this issue, Michael Ludwig and colleagues show that one exception is in an enhancer region of a key developmental gene in fruitfl ies of the genus Drosophila. Here, the enhancer is functionally similar enough in two species that diverged 60 million years ago that switching them produces normal development, but different enough in two species separated by only 10 million years that exchanging them between the two fl ies aborts development. The gene in question is even-skipped, a patterning gene that creates seven transverse stripes along the anteriorposterior axis in the fruitfl y embryo. Its expression is regulated by fi ve enhancing elements located upstream from the promoter. The best characterized of these, the stripe 2 enhancer (S2E), binds fi ve different transcription factors at multiple locations.
Ludwig et al. deleted S2E in D. melanogaster, and then added back S2E from one of four Drosophila species: D. melanogaster itself; D. yakuba or D. erecta, both of which have been separated from D. melanogaster for 10-12 million years; or D. pseudoobscura, which split from the D. melanogaster line 40-60 million years ago. Despite serving identical functional roles in each species, the structures of these enhancers differ, with large deletions and insertions between transcription factor binding sites, as well as other changes. Nonetheless, within each species, the spatiotemporal pattern of expression induced by S2E is essentially identical, suggesting that, despite their structural differences, they might be functionally interchangeable.
Since loss of S2E is lethal, the viability of the embryos that resulted from these experiments gives a measure of each enhancer's ability to function in its new environment. The authors found that while viability of D. melanogaster with the D. pseudoobscura S2E was identical to that with D. melanogaster's own, viability with S2E from the more closely related D. erecta was almost zero, essentially the same as not having the enhancer at all. S2E from D. yakuba impaired the viability of D. melanogaster as well, although not as much as that from D. erecta. Viability was closely correlated with the level of stripe 2 expression induced by each S2E, with very low levels induced by the D. erecta enhancer and normal levels by that of D. melanogaster and D. pseudoobscura.
Why did the D. erecta enhancer fail to respond in the D. melanogaster environment? Ludwig et al. suggest it may be due to a change in the sensitivity of the "set point" in D. erecta's enhancer, which acts like an on-off switch governing gene expression, making the enhancer unresponsive to the gradients of transcription factors found in D. melanogaster. This change may be due to relatively small differences in the two species' enhancers that have accumulated since their evolutionary split.
The results of this study indicate an important caveat about interpreting the evolution of gene regulatory regions. As a complex functional unit that integrates a host of signals, the S2E is likely to be under strong stabilizing selection, maintaining its output within narrow limits. Thus, the phenotypic result of the enhancer-the location and timing of stripe formation it induces in its native environment-remains conserved among the four species. However, unlike an enzyme or structural protein, in which structural changes are tightly constrained by their effects on function, the structure of any particular enhancer need not be so rigidly preserved. As long as the consequences of change in one region, such as loss of a transcription factor binding site, are matched by compensatory changes in another, such as gain of one, or, as Ludwig et al. speculate, by complementary changes in genetic background, the fi nal output of the enhancer can remain the same. Thus, the utility of structural similarities in understanding evolutionary relationships is likely to be less for gene regulatory regions than for structural genes or the proteins they encode. live) to establish winter trends and model wolves' impact on the fate of resident scavengers faced with a changing climate. Not surprisingly, their models show that this top predator exerts signifi cant infl uence over animals at lower levels in the food chain: wolf kills temper the potentially devastating effects of climaterelated carrion shortages on scavengers. Unlike mountain lions and grizzly bears, wolves abandon their prey (usually elk or moose) once sated, leaving much-coveted leftovers for ravens, eagles, coyotes, bears, and other scavengers. These fi ndings indicate that individual species stand a better chance of adapting to climate change in an ecosystem with an intact food chain.
Wilmers and Getz's weather data analysis found that both late-winter snow depth and snow-cover duration have decreased signifi cantly since 1948-winters in Yellowstone are getting shorter. That's good news for elknavigating deep snow taxes stamina and reduces access to forage-but bad news for scavengers that rely on elk carcasses to carry them through the winter.
The authors generated two sets of models to estimate the effects of shorter winters on the wolf-elk-scavenger dynamics. In the fi rst, late-winter carrion availability drops by 66% without wolves but by only 11% when the predators are present. The second model examines the impact of elk and wolf population dynamics on carrion availability. This analysis predicts that more elk will die in early winter than in late winter, a scenario that favors eagles and ravens-which can cover a lot of ground quickly-over bears and coyotes. Altogether, these modeling studies show that shorter winters without wolves will create intermittent food supplies that no longer track the needs of local scavengers. With or without wolves, late-winter carrion abundance will decline with shorter winters. But wolf kills buffer these shortages, providing meals that could determine whether scavengers will be able to survive and reproduce.
It seems clear that wolves have the potential to provide a safety net for scavengers, extending the time they need to adapt to a changing environment. Thanks to a rebounding wolf population, fi eld researchers can measure the magnitude of this predicted buffer effect. The models described here can guide their efforts and help species adjust to major environmental shifts like climate change.
As a young US ranger "full of triggeritch," Aldo Leopold killed his share of wolves under the federal eradication policy-until he "watched a fi erce green fi re dying" in the eyes of a slain mother fl ush with pups and realized he had not understood the wolf's ecological role. Wilmers and Getz's study shows that a robust food chain-including this still embattled top predator-may be even more important as ecological conditions deteriorate. It's been known for a long time that only 2%-3% of human DNA codes for proteins. Much of the rest of our genomes-often referred to as junk DNA-consists of retroelements: genomic elements that are transcribed into RNA, reverse-transcribed into DNA, and then reinserted into a new spot in the genome. Human endogenous retroviruses make up one class of these retroelements. Retroviruses can insinuate themselves into the host's DNA in either soma (nonreproductive cells) or the germline (sperm or egg).
If the virus invades a nonreproductive cell, infection may spread, but viral DNA will die with the host. A retrovirus is called endogenous when it invades the germline and gets passed on to offspring. Because endogenous retroviruses can alter gene function and genome structure, they can infl uence the evolution of their host species. Over 8% of our genome is made of these infectious remnants-infections that scientists believe occurred before Old World and New World monkeys diverged (25-35 million years ago).
In a new study, Evan Eichler and colleagues scanned fi nished chimpanzee genome sequence for endogenous retroviral elements, and found one (called PTERV1) that does not occur in humans. Searching the genomes of a subset of apes and monkeys revealed that the retrovirus had integrated into the germline of African great apes and Old World monkeys-but did not infect humans and Asian apes (orangutan, siamang, and gibbon). This undermines the notion that an ancient infection invaded an ancestral primate lineage, since great apes (including humans) share a common ancestor with Old World monkeys.
Eichler and colleagues found over 100 copies of PTERV1 in each African ape (chimp and gorilla) and Old World monkey (baboon and macaque) species. The authors compared the sites of viral integration in each of these primates and found that few if any of these insertion sites were shared among the primates. It appears therefore that the sequences have not been conserved from a common ancestor, but are specifi c to each lineage. PTERV1 contains three structural genes-gag, pol, and env-and regulatory sequences called long terminal repeats (LTRs). To further explore the evolutionary history of the retroviral elements, the authors compared the sequences of gag and pol, as well as the LTR sequences, for each infected primate species. The sequence history, they discovered, did not comport with the established evolutionary history of the primates themselves. Divergence between macaque and baboon was signifi cantly greater than between gorilla and chimp-even though slightly more evolutionary time separates gorilla and chimp than macaque and baboon.
When a retrovirus reproduces, identical copies of LTR sequences are created on either side of the retroviral element; the divergence of LTR sequences within a species can be used to estimate the age of an initial infection. Eichler and colleagues estimate that gorillas and chimps were infected about 3-4 million years ago, and baboon and macaque about 1.5 million years ago. The disconnect between the evolutionary history of the retrovirus and the primates, the authors conclude, could be explained if the Old World monkeys were infected by "several diverged viruses" while gorilla and chimpanzee were infected by a single, though unknown, source.
As for how this retroviral infection bypassed orangutans and humans, the authors offer a number of possible scenarios but dismiss geographic isolation: even though Asian and African apes were mostly isolated during the Miocene era (spanning 24 to 5 million years ago), humans and African apes did overlap. It could be that African apes evolved a susceptibility to infection, for example, or that humans and Asian apes evolved resistance. A better understanding of the evolutionary history and population genetics of great apes will help identify the most likely scenarios. And knowing how these retroviral elements infi ltrated some apes while sparing others could provide valuable insights into the process of evolution itself. In the intricate dance of animal development, several critical steps are choreographed by the Notch receptor and its ligands, including Delta (Dl) and Serrate (Ser). When these ligands bind, an intracellular segment of the receptor is cleaved off and becomes a transcriptional regulator within the nucleus. While Dl and Ser both occur in Drosophila, and appear to have similar interactions with Notch, less is known about exactly how they trigger Notch activity. In particular, few details are known about the activators of Dl and Ser, which begin the cascade ultimately leading to Notch signaling. In this issue, François Schweisguth and colleagues show that two activators, Drosophila mind bomb (D-mib) and Neuralized (Neur), while sharing a similar molecular activity, have distinct roles in Notch-related Drosophila development, and elucidate several important activities of the heretofore mysterious D-mib.
D-mib and Neur are ubiquitin ligases, enzymes that attach the small protein ubiquitin onto a target protein. While ubiquitination was fi rst appreciated as a tag for protein degradation, more recently, it has been recognized to be a signal for endocytosis, a process that brings substances outside a cell into the cell. Endocytosis, in turn, has recently been found to be a key step in Dl activation of Notch; its importance to Ser signaling has not been previously identifi ed. In Drosophila, Neur targets Dl, and Dl is endocytosed. In zebrafi sh, Dl is a target for a separate ubiquitin ligase, Mind bomb. But the function of the Drosophila homolog, D-mib, has not been elucidated. Thus, the essential questions in this study were, what role does D-mib play in Drosophila, and how is Ser signaling regulated?
Schweisguth and colleagues studied development in a D-mib mutant. The pattern of phenotypic changes seen was in keeping with a loss of Dl signaling, indicating that D-mib interacts with Dl, just as Neur does. But D-mib also interacts with the other Notch ligand, Ser, as shown by the aberrant distribution of Ser in the absence of D-mib. Furthermore, endocytosis of Ser occurred normally in the presence of D-mib, and was strongly inhibited in its absence. Acting through Notch, Ser activates a downstream gene that codes for a protein called Cut, whose absence leads to a particular pattern of wing defects. This pattern was seen in D-mib mutants, and could not be rescued by overexpressing Ser, thus indicating that D-mib not only prompts endocytosis of Ser, but allows it to trigger Notch signaling. It's unclear whether D-mib ubiquitinates Ser, as this study did not specifi cally address that question.
While Neur and D-mib differ structurally, they share the same molecular function, ubiquitination of Notch ligands, and the authors show that, when ectopically expressed, each can at least partially compensate for the absence of the other. Nonetheless, they normally have distinct developmental functions, owing largely to the fact that they are expressed in different locations and at different times during development, and thus mutations in the two lead to different patterns of developmental aberrations. More than a billion people are at risk for infection with fi larial nematodes, parasites that cause elephantiasis, African river blindness, and other debilitating diseases in more than 150 million people worldwide. The nematodes themselves play host to bacteria that live within their cells, but in this case, the relationship is classic mutualism, with each benefi ting from the other. Indeed, the Wolbachia bacterium is so crucial to its host nematode that apparently eradicating it with antibiotics severely compromises the nematode's ability to complete its life cycle within its human host. Thus, understanding the details of this symbiosis may help identify new strategies for controlling diseases caused by fi larial nematodes. In a new study, Barton Slatko and colleagues present the complete DNA sequence of the Wolbachia pipientis strain within Brugia malayi, a parasitic nematode responsible for lymphatic fi lariasis, and analyze its genome for clues to the interdependence of the two species.
This Wolbachia genome is small, only about a million base pairs, and many metabolically critical genes have degraded through mutation to the point of uselessness. This phenomenon, called reductive evolution, is typical of longterm symbioses, as the two partners increasingly complement one another's biochemical activities, reducing the selection pressure on otherwise lethal mutations. Wolbachia's translational machinery and DNA repair equipment are largely intact. The bacterium appears to supply nucleotides to its host, as it contains complete pathways for biosynthesis of both purine and pyrimidine nucleotides. This is in contrast to Rickettsia, a close relative of Wolbachia and a mammalian parasite. Slatko and colleagues enumerate a variety of other pathways that have either been degraded or preserved, and highlight patterns in the genome structure through comparisons with both Rickettsia and another Wolbachia strain, found in fruit fl ies. For example, the two Wolbachia strains appear to have different membrane structures, possibly refl ecting their different lifestyles (mutualistic versus parasitic).
Wolbachia can manufacture ribofl avin and FAD, which are essential metabolic coenzymes and which do not appear to be made by its host. Conversely, it cannot synthesize amino acids and a variety of other vitamins and cofactors, and probably depends on the nematode to supply them. One discovery of possible signifi cance is the presence in the bacterium of the synthetic pathway for heme-the oxygencarrying iron component of hemoglobin. The nematode may require heme for synthesis of developmental hormones, so Wolbachia's heme pathway may be an inviting target for therapy against nematode infection. Since no new antifi larial has been developed in two decades, these results may quickly lead to new therapeutic strategies against these parasites. And Littler Genomes inside 'Em: Clues to a Parasitic Nematode's Bacterial Partnership DOI: 10.1371/journal.pbio.0030148 Fungi live mainly in the dark, and they like it that way-out of the sunlight, they can avoid desiccation and damage from ultraviolet rays. The ability to sense light, therefore, is adaptive for fungi of all kinds. A pair of light-sensing proteins had been identifi ed in the model fungus Neurospora crassa, an ascomycete (one of the three fungal subgroups, defi ned by the production of sexual spores within sac-like structures), but little was known about mechanisms in other fungal phyla. In a new study, Alexander Idnurm and Joseph Heitman show that the basidiomycete (a subgroup defi ned by the production of sexual spores on the ends of club-like structures) Cryptococcus neoformans employs a similar protein pair, which regulate mating, growth, and virulence of this human fungal pathogen.
In N. crassa, blue light is sensed by the protein White collar 1, which interacts with a fl avin (light-absorbing pigment) tuned to photons in the blue region of the spectrum. White collar 1 then binds to White collar 2, and the complex serves as a transcription factor. In this study, the authors searched the C. neoformans genome for genes with similar evolutionary origins to these two genes (called homologs), as well as others implicated in light sensing, and identifi ed Basidiomycete white collar 1, or BWC1, along with other light-sensor candidates, including an opsin and a phytochrome homolog. Mutations of BWC1, but not the other candidate photoreceptors, rendered C. neoformans insensitive to light. While mating and fruiting in the wild-type fungus is suppressed by exposure to blue light, bwc1 mutants were unaffected by light. Interestingly, the mating process was released from light inhibition when either one of the two mating strains were mutated, suggesting that the cell fusion process at the heart of fungal mating requires only one cell to commit to fusion. In addition, bwc1 mutants were extremely Adjusting to life after birth takes a lot of energy. One way cells meet increased demand is by ramping up synthesis of mitochondria, the cells' power generators. This ability to increase mitochondria becomes limited in a variety of diseases including diabetes and heart failure. Therefore, it is important to identify the factors that control mitochondrial function. One way researchers have searched for candidate proteins that play a role in this process is by overexpressing proteins in targeted cells to see what happens. That's how several previous studies concluded that a protein called PGC-1α triggers pathways that promote mitochondrial synthesis and regulate both mitochondrial activity and energy metabolism.
In a new study, Daniel Kelly and colleagues took a different approach. Rather than increasing the protein's activity, they blocked it. To do that, Kelly and colleagues engineered "knockout" mice that lack functional copies of the PGC-1α gene. PGC-1α, they found, isn't absolutely required for mitochondrial biogenesis but plays a vital role later in life by "boosting" the ability of cells to increase mitochondrial function in response to the shifting energy demands and physiological stresses encountered after birth.
Though leaner than the control mice soon after birth, by 18 weeks the female knockouts were slightly heavier and had more body fat, even though their food intake and activity levels matched the controls. Knockout mice had observable growth defects in skeletal and heart muscle-tissues with high mitochondrial energy requirements-were less active and more easily fatigued than the controls, and had abnormal heart rates after physical exertion. And their livers showed a propensity to accumulate fat because of abnormal mitochondria.
Altogether, these results demonstrate PGC-1α's critical role in regulating the adaptive metabolic responses required by the increasing energy demands and changing physiological stimuli associated with a growing organism. The increased fat stores and weight gain in the knockout mice, the authors propose, could result from a systemic reduction in energy use, related to defective mitochondria. Given the recently reported link between PGC-1α mutations and human obesity and diabetes, this connection will likely trigger further investigations. And given the pivotal role mitochondria play in a wide range of organs, this mouse model could help shed light on metabolic defects associated with a wide range of diseases. Interestingly, another group, led by Bruce Spiegelman, reported on a PGC-1α knockout model last year. Their mice share traits with the mice described here, but also exhibit a number of contrasting traits, including hyperactive, lean males, which the Spiegelman group attributed to a neurological defect. Kelly and colleagues speculate on possible causes for the differences in the results of the two studies, but only direct comparison of both mouse models will explain the inconsistencies. sensitive to ultraviolet radiation. No homolog of photolyase, a protein that uses light to repair DNA damage, was identifi ed in the genome. Future studies will be necessary to understand how Bwc1 functions in ultraviolet resistance, but these fi ndings suggest the protein could sense photons in both the ultraviolet and blue wavelengths.
To identify other proteins with which the Bwc1 protein functionally interacts, the authors examined nearly 3,000 mutant strains, yielding three with a phenotype similar to the bwc1 mutant. They found that the gene for one of these, dubbed BWC2, is a homolog of N. crassa White collar 2, and that its protein binds to Bwc1. Together, the two infl uence transcript levels of two key genes required for C. neoformans mating, further strengthening the case that the pair function as a transcription factor as do their homologs in N. crassa. Interestingly, mutants of either BWC1 or BWC2 were less virulent than the wildtype strain of the fungus, revealing a novel environmental signaling pathway involved in C. neoformans virulence.
The functional and structural similarities of the ascomycote and basidiomycote White collar proteins indicate that they arose prior to the split of these two lineages more than 500 million years ago. The fungal kingdom contains an estimated one million species. The authors suggest that the ultraviolet protection afforded by the White collar system may have been crucial to the evolutionary diversifi cation of this kingdom, in particular when ultraviolet radiation on the earth's surface was higher than it is today, such as when life emerged from the sea and colonized the barren continents. They also note that the same proteins are found in clinical isolates of C. neoformans, and that the mitigation of virulence by bwc1 and bwc2 mutations will be useful in the identifi cation of new genes required for disease development in this important pathogen. For a virus to survive, it must elude the ever vigilant immune sentinels of its host. A latent virus can escape immune detection if it resides in nondividing cells and doesn't produce any proteins. No viral proteins means no red fl ags for immune cells. If the virus targets one of the many cell types that rarely divide, it's relatively safe while latent. But some viruses, like the gamma-herpesvirus, infect B cells of the immune system, which occasionally divide. The gammaherpesvirus genome persists as circular pieces of DNA called episomes. When an infected B cell divides, the latent gammaherpes virus episome must replicate and segregate into daughter cells along with the cell's genome. Viral replication and segregation requires the services of a protein called the episome maintenance protein-a potentially recognizable target for immune cells.
Gamma-herpesviruses, including Epstein-Barr virus (EBV) and Kaposi's sarcoma-associated herpesvirus (KSHV), can induce uncontrolled lymphocyte (immune cell) proliferation and result in lymphoma, Hodgkin's disease, and Kaposi's sarcoma. These diseases arise from the persistent latent infections that take hold after initial infections are controlled by immune defenses. The episome maintenance protein produced by EBV, called EBNA-1, harbors an amino acid element in its epitope-the region that binds to a T cell and triggers an immune response-that helps the viral protein evade the killer T cells that could destroy it. Lab studies show that the amino acid element limits EBNA-1's interaction with T cells by inhibiting synthesis and, to a lesser degree, degradation of the protein. How this evasive action works or helps the virus in a living organism is not entirely clear. But if T cells aren't presented with bits of viral protein, they have no way of knowing the virus is present.
In a new study, Neil Bennett, Janet May, and Philip Stevenson explore this question by studying virus-host interactions in mice infected with the murine gamma-herpesvirus-68 (MHV-68). Though MHV-68 infects mice, it behaves similarly to EBV and KSHV infections in humans, producing an acute mononucleosis-like illness and a pervasive pool of latently infected B cells. The episome maintenance protein in MHV-68 and KSHV is called ORF73. None of the viruses can maintain latent infections with defi cient episome maintenance proteins.
Stevenson and colleagues fi rst demonstrated that ORF73 limits T cell recognition and then identifi ed a key region responsible for immune evasion by modifying different regions of the viral protein. In the next round of experiments, the authors asked how the viral protein manages this feat. They discovered that ORF73 limits T cell recognition much like EBNA-1 does, by reducing synthesis and degradation of the protein.
One region strongly associated with inhibiting epitope presentation to killer T cells corresponded to reduced protein synthesis. When the authors modifi ed the ORF73 transcript to circumvent T cell evasion, the T cells "wiped out" latent virus. These results indicate that avoiding epitope presentation during episome maintenance is key to the virus's survival.
Interestingly, the MHV-68 episome maintenance protein mediates immune evasion even though it lacks the amino acid element that does the job for EBV. Future studies will have to determine the responsible MHV-68 epitope and the mechanisms that engineer immune avoidance. Since a majority of epitopes that killer T cells recognize come from aborted translation events, it may be that evasive action is taken at the RNA transcript stage, before RNA is translated into protein. Evading killer T cells, the authors argue, is key to the survival of the gamma-herpesvirus. By fi guring out just how evasion occurs, scientists can identify a promising target for controlling infection. For Proust, a taste of cookie was enough to trigger vivid recollections of his childhood, the fi rst of a long string of reveries that he fashioned into his famous memoir Remembrance of Things Past. For many animals, too, tastes and smells are evocative and play a crucial role in fi nding food, allowing them to build on past successes and to learn how to fi nd their next meal.
To locate blooming fl owers, for example, honeybees rely heavily on scent.
They can associate a whiff of an aldehyde, say, with a nectar-fi lled orchid. Then later they'll seek out the same or similar scents. To succeed in the wild, they must be able to distinguish relevant scents at varying concentrations, and within complex milieus of other scents. But to fi nd food in varied conditions and adapt to new situations, they also have to generalize from past experience.
Through both physiological and behavioral studies, scientists have investigated the response to smell in a wide range of organisms and have suggested that two key properties of scent-inducing chemicals are the functional class, such as alcohol or aldehyde, and the carbon-chain length. Bees trained to associate a particular chemical with a reward, for example, can then generalize to some extent to other chemicals with the same functional groups or similar carbon-chain lengths. In these situations, bees are surprisingly

MHV-68 virions emerging from infected
cells consistent in both in their behavior (extending their proboscis to an odor previously associated with food) and in their brains (brain activity in smellprocessing centers). Each set of data, behavioral and neural, can be thought of as a "code" underlying the bee's response: present a scent, and a bee's brain and body will tend to react in a certain way.
A new study of smell perception in honeybees (Apis mellifera) published in PLoS Biology gives a more comprehensive picture of how bees react to a suite of scents and also shows a remarkable correspondence between the codes for the insects' behavior and brain activity. The researchers, led by Martin Giurfa, fi rst trained bees to associate a specifi c chemical, such as the alcohol 1-nonanol, with a sucrose reward. Then the researchers tested the bees' response to a set of other chemicals, varying in carbon-chain length from six to nine, and with four different functional groups: aldehydes, ketones, and primary and secondary alcohols.
By watching how often the bees generalized-that is, how often they responded positively to a particular scent when they'd been trained on anotherthe researchers could assign perceptual "distances" between pairs of chemicals. Drawing together all these distances, they created a preliminary map of the bees' "perceptual space," similar to how surveyors measure distances between landmarks to map a landscape. From this comparison they found, for example, that the bees generalized more by functional group than by carbon-chain length.
Previously, Giovanni Galizia's group, which works closely with Giurfa's group, had recorded bees' brain responses to the same pairs of scents, assigning distances within centers of activity for each scent. Giurfa's team compared these two sets of data and found that the perceptual and neural distances correlated well, which suggests there's a species-specifi c code that ties together the insects' brain and behavior.
The brain recordings covered only a quarter of the bees' main smellprocessing center, the antennal lobe. Future studies with new methods of microscopy that visualize more of the brain and which focus on the olfactory message sent by the antennal lobe to higher-order brain centers should only improve our ability to investigate the correlations between brain and behavior, the authors say. Such studies would go even further toward cracking the codes underlying animals' perception and memory.

Guerrieri F, Schubert M, Sandoz J-C, Giurfa M (2005) Perceptual and neural olfactory similarity in honeybees. DOI: 10.1371/ journal.pbio.0030060
For most of human history, cancer has been incurable. But with the invention of anesthesia in the mid-19th century, surgeons were able to remove some forms of cancer surgically. Radiotherapy arrived next, soon after the discovery of X rays in 1896. Chemotherapy, now a mainstay of cancer treatment, did not arrive until the mid-1940s, when nitrogen mustard, an alkylating agent related to the mustard gas used in the two World Wars, was developed as an anticancer agent. Unfortunately, although cancer cells are hypersensitive to the effects of alkylating agents-molecules that introduce lethal changes into the cell's DNA-normal cells are also targeted by them, although less damage is caused because normal cells typically divide slower than cancer cells. Using chemotherapy based on alkylating agents to treat cancer is like using a sledgehammer to crack a nut. But with improved knowledge about how cancer cells differ from normal cells, chemotherapeutics are now being designed that hit only cancer cells.
Many of these new chemotherapeutics target protein receptors called tyrosine kinases. These receptors, which sit on the cell surface, normally stimulate intracellular pathways that control proliferation and other cellular functions in response to growth factors. In tumors, these receptors often have mutations that allow them to become active without growth factor binding, which results in the uncontrolled proliferation that is characteristic of cancer cells. For instance, mutations in the RET receptor tyrosine kinase are responsible for multiple endocrine neoplasia (MEN) type 2 syndromes. Whereas external stimulation by a growth factor is normally needed before two RET molecules can bind together (a process called dimerization) to activate intracellular signaling cascades, in MEN type 2A, a mutation in the RET receptor tyrosine kinase provokes (or induces) dimerization without external stimulation.
In recent years, several proteins and various small synthetic chemicals have been designed that specifi cally inhibit the activity of mutated receptor tyrosine kinases and show anticancer activity. Domenico Libri and colleagues are now working on another class of molecules, called aptamers, that have potential as anticancer drugs. Aptamers-singlestranded nucleic acid molecules that are 50-100 bases long and can be selected for their ability to bind directly and tightly to specifi c proteins-are less likely to be targeted and destroyed by the body's natural defenses than some other types of potential therapeutic molecules. To fi nd an aptamer able to recognize the RET receptor kinase within a cellular membrane environment, the researchers used whole-cell SELEX (systematic evolution of ligands by exponential enrichment), a process in which large pools of oligonucleotides are enriched for molecules that can distinguish between a real and sham target. First, they incubated a large pool of RNAs with PC12 cells, a rat cell line not expressing A Small RNA That Neutralizes a Protein Linked to Tumor Development RET, to remove sequences binding non-specifi cally to the PC12 cell surface. Unbound sequences were recovered and applied to PC12 cells expressing human RET with the MEN type 2A mutation that causes dimerization. This time, bound sequences were retained, and the whole selection process was repeated another 14 times to select for aptamers that recognize the dimeric form of the RET extracellular domain.
Of the 67 sequences pulled out of the fi nal pool of RNAs, the researchers found one sequence, D4, that not only bound the extracellular domain of RET but also blocked RET downstream signaling events and subsequent cellular and molecular changes. The researchers suggest that D4 blocks the dimerizationdependent activation of RET-whether it's induced by its physiological signaling molecule or by an activating mutation-and suggest that their method can be used to identify macromolecules with potential therapeutic effects against other transmembrane receptors involved in tumorigenesis, particularly since the whole-cell SELEX approach should effi ciently select aptamers that recognize these receptors as they are found on the surface of tumor cells. From The Worst Case Scenario Survival Handbook-with handy entries like "How to escape from killer bees" and "How to escape from quicksand"-to The Zombie Survival Guide: Complete Protection from the Living Dead, survival guides are one of the latest publishing fads.
If there was a market for it, a survival guide for bacteria might include topics like "How to use your pili to keep your host from going apoptotic." A host's cells can respond to a bacterial infection with apoptosis, or programmed cell death. For bacteria that pass directly from host to host, this can pose a problem. If the bacteria are highly virulent and induce too much cell death, they could take down their host before they're able to jump ship, thus hurting the bacteria's chances of survival in the long run.
Earlier studies suggested that bacteria can use their pili, fi nger-like appendages that many bear on their surface, to pull on a host's cell membranes and thus infl uence the cell's behavior. But these studies, which looked at mutant bacteria that could not retract their pili, did not examine the matter of how the bacteria coax their hosts to stay alive. Now, in PLoS Biology, a group of researchers present more direct evidence that bacteria can induce changes in hosts' gene expression-and possibly keep the host cells alive longer-through tiny tugs on cell membranes. The study, led by Magdalene So, examined gene activity in human epithelial cells infected with Neisseria gonorrhoeae, the bacteria responsible for the sexually transmitted disease gonorrhea.
By comparing cells infected with normal N. gonorrhoeae to those infected with a mutant strain with defective pili, the researchers found a subset of 52 host genes that had higher activity when the host was infected with the normal bacteria, suggesting that the pulls of the pili were responsible. They also ran a key control experiment with an artifi cial mechanical pull on the host cell membrane. By coating magnetic beads with a preparation of bacterial pili, the beads attached themselves to the cell membranes. Then, in the presence of a magnetic fi eld, the beads tugged on the cell membrane, approximating the effects on gene expression during infection with normal bacteria.
Thus, the mechanical tugs seem responsible for triggering a signaling cascade in the host cells, which ultimately affects the host's gene expression. Many of the genes that increased in activity due to the tugs were already known to regulate apoptosis and cellular response to stress, including mechanical strain on the membrane. Also, a majority of these genes were known to be induced by a family of proteins called mitogenactivated protein kinases, or MAPKs. The researchers showed that blocking MAPKs reduced the activity of several of the genes that are usually enhanced by infection with the normal bacteria. Also, they found that cells infected with the bacteria tended to survive treatment with staurosporine, a chemical that normally induces apoptosis.
Overall, the group's fi ndings support previous speculations that some bacteria infl uence gene expression and the fate of cells in their hosts by tugging on the host cells' membranes with their pili. For bacteria like N. gonorrhoeae that pass directly from host to host, the researchers argue, it would be in a bacterium's interest to help keep its host alive. And bacteria appear to do this with the help of their pili. We all know that our memories are stored somehow in our brains. But exactly how do we remember the way to our offi ce or what our mother looks like or the date we got married? Scientists attribute our ability to store apparently infi nite numbers of memories for decades to long-lasting changes in the electrical, structural, and biochemical properties of neurons. One cellular mechanism proposed to be involved in the storage of memories-long-term potentiationinvolves alterations in the strength of messages passed from one neuron to another across structures known as synapses.
The initiation of long-term potentiation is caused by activation of N-methyl-Daspartate receptors on the receiving neuron and a subsequent increase in the intracellular calcium concentration in a region of the neuron that is called the postsynaptic density. The increase in calcium, in turn, activates the calcium/ Memories Are Made of This: Modeling the CaMKII Molecular Switch DOI: 10.1371/journal.pbio.0030124 When you think of the cell as the fundamental unit of life, it's not surprising that some organs deal with injury better than others. A fl esh wound or muscle tear might hurt, but, assuming you are otherwise healthy, both will heal. The prognosis for a heart attack, on the other hand, is not so clear-cut. What accounts for the difference?
Skin cells reproduce regularly to replace dead cells, and simply increase production in the event of injury. Skeletal muscles recruit new muscle cells from a type of precursor cell within the muscle, called satellite cells, to repair a tear. Cardiac cells (cardiomyocytes), it has long been thought, appear to lack this capacity for self-renewal and repair, impeding the chances of a full recovery. That's why therapies derived from stem cells-which retain a unique ability to morph into any of the body's 200-plus cell types-hold such promise. But stem cells are a hot-button issue in the United States, complicating efforts to explore this promise.
Recent evidence suggests that the heart might harbor stem cells after all and that such cells can be transformed into cardiomyocytes. In a new study, Neal Epstein and colleagues report that cells isolated from the skeletal muscle of adult mice can turn into beating cardiomyocytes in a test tube within days of isolation-and without the addition of gene-altering drugs or special cardiac factors. When freshly isolated cells (called skeletal precursors of cardiomyocytes, or Spoc cells) are injected into the tail veins of mice with heart damage, they migrate to the damaged tissue and differentiate into cardiac muscle cells.
What distinguishes a cardiomyocyte from a skeletal muscle cell? Specialized cells produce unique proteins, allowing scientists to use those proteins as identifying markers. The so-called Spoc cells do not express any of the usual markers associated with either skeletal muscle satellite cells or partially differentiated skeletal muscle cells. By day 7 in culture, Spoc cells have undergone several rounds of cell division and have begun to express a (mostly) cardiacspecifi c protein, and have formed clusters of cardiac precursor cells, some of which beat. These precursors in turn express other cardiac-specifi c proteins.
Epstein and colleagues further divided Spoc-derived precursor cells into two groups based on whether or not they expressed another protein marker (Sca-1, a common marker found on blood stem cells). About 80% of cells without this protein differentiated into immature beating cells after proliferating for seven to ten days. They remained in an immature state (round and loosely attached) for over two months in culture, but differentiated into mature beating heart cells (elongated and adherent) when mixed with Sca-1 cells. The authors use video microscopy to track the cells' progression to beating cells, complete with contraction-generating thick myosin fi laments that are "nearly identical" to those seen in developing cardiomyocytes. Epstein and colleagues also demonstrate that the Spoc cells are distinct from stem cells cultured out of bone marrow, heart, or fat tissuesources of beating cells in other studies. The authors also injected these Spoc cells into mice with acute heart lesions to test the cells' ability to integrate into the damaged tissue. Many cells successfully migrated to and engrafted into the site of injury; some of these cells developed into cardiomyocytes. The cells showed a similar, though less robust, response to an older heart injury.
Epstein and colleagues argue that Spoc cells are more likely to be precursors to cardiomyocytes than to be some other type of skeletal muscle stem cell. This is based on an absence of protein markers for skeletal muscle or skeletal satellite cells in Spoc cells, as well as the fact that Spoc-derived cells display spontaneous rhythmic beating and express cardiac markers, whether they are grown in a test tube or have migrated to injured hearts in study mice. The authors can't say why skeletal muscle would harbor cardiac stem cells or why so few of these cells pitch in to repair a cardiac injury. But for now, the Spoc cells provide a valuable tool for studying heart cell differentiation.

Spoc cells can help repair a damaged heart
Protecting the liver from infection presents the immune system with a tough challenge. Because it is the fi rst stop for food absorbed from the gut, the liver is constantly bathed in a rich broth of mostly harmless foreign molecules, which need to be immunologically tolerated. On the other hand, the slow rate of blood fl ow and high internal surface area makes the liver's many sinuses ideal sites for infections to take hold. One unusual type of immune cell patrolling this complex maze in the liver is the natural killer T (NKT) cell. In this issue, Dan Littman, Mike Dustin, and colleagues shed some light on the behavior of this littleappreciated and important hepatic guardian, showing its unexpected ability to perform immune surveillance entirely within the vasculature. NKT cells crawl along vascular passages in the liver (hepatic sinusoids) at high speeds for a cell moving under its own power, but slow speeds compared to blood fl ow, and never or rarely venture into the surrounding tissue.
To track the movements of these cells, the authors used a mouse in which the gene for the CXCR6 receptor was replaced with a gene for green fl uorescent protein (GFP). In these mice, cells that express CXCR6 also express GFP, and because they fl uoresce, they can be visualized and tracked under a microscope. The study showed that cells remained entirely within the blood vessels, crawling along the endothelial lining at approximately 16 microns per minute. Despite directional blood fl ow, the NKT cells moved and changed directions randomly, and could occasionally be seen migrating past one another in opposite directions within a single vessel. When the authors injected antigen into the blood stream, the cells abruptly stopped, and remained stationary, suggesting that they had fulfi lled their fi rst duty to fi nd antigen and were beginning their next: to alert the rest of the immune system. Surprisingly, antigen detection occurred within the blood stream-it is normally calmodulin-dependent protein kinase II (CaMKII). This enzyme seems to play a critical role in long-term potentiation, and has been proposed as one of the leading candidates to act as the molecular switch that maintains stable synapse-specifi c cellular changes. To fulfi ll this role, CaMKII would need to have stable UP and DOWN positions, or states, much like a light switch. Xiao-Jing Wang and colleagues now provide a new analysis that strengthens the argument that CaMKII is a molecular switch involved in the storage of longterm neural changes. The activity of the CaMKII holoenzyme (the complete enzyme consisting of both regulatory and catalytic subunits) is controlled by its autophosphorylation state-the enzyme is able to add phosphate groups to specifi c amino acids within itself. Previous modeling studies have shown that the interplay between the autocatalytic addition of phosphate groups to CaMKII and the removal of phosphate groups by protein phosphatase-1 (PP1) enzymes produces two stable states of the CaMKII enzyme at basal free calcium levels. The DOWN state is unphosphorylated; the UP state is highly phosphorylated. When there is a transient high input of calcium, as happens when long-term potentiation is induced, the CaMKII enzyme fl ips from a DOWN state to a persistent UP state.
The questions that Wang and colleagues have now asked are what factors affect the stability of the state of this switch, and how many CaMKII holoenzymes are needed to construct a switch that could last a lifetime. These questions are important because a switch that could be spontaneously reset by small, random fl uctuations of the conditions within the postsynaptic density would not be useful in maintaining stable long-term changes. The researchers have used a mathematical probabilistic modeling technique known as Monte Carlo simulation, together with the known biochemical and thermodynamic characteristics of CaMKII and PP1, to test how random fl uctuations in the chemical reactions involved in the CaMKII/PP1 system change the state of the switch.
They report that switch state stability requires a balance between the phosphorylation and dephosphorylation rates of CaMKII, and that the turnover rate of the kinase-the replacement of old molecules with new ones-critically affects switch stability. However, their main fi nding is that the lifetime of states of the switch increases exponentially with the number of CaMKII holoenzymes that are present. This fi nding is important because experimental work by other researchers has estimated that there are about 30 CaMKII holoenzymes present in a typical postsynaptic density, and until Wang's team did their modeling it was unclear whether this number of holoenzymes could build a switch stable enough to last a lifetime. In fact, Wang and co-workers estimate that a switch containing as few as 15 holoenzymes can remain activated for longer than a human lifetime. Thus, the researchers conclude, CaMKII switches may indeed play a critical role in preserving our precious memories throughout our lives. Tracking the movment of glowing T cells in the vasculature thought to occur after lymphocytes leave the blood.
While they make up less than 1% of lymphocytes in other tissues, NKT cells comprise 30% of the lymphocytes in the liver. Mice lacking both copies of the cxcr6 gene had only one third the normal number of hepatic NKT cells. Though chemokine receptors are typically thought to function by directing cell homing, the authors observed that CXCR6-defi cient cells died rapidly in vitro, suggesting that CXCR6 delivers survival signals and thereby controls the number of hepatic NKT cells and liver immune surveillance in general.
While cell numbers were reduced, the movement of the remaining cells in the homozygous-deleted mice was no different than that in the heterozygotes. Because of this, the authors propose that cell motility in wild-type mice is likely to be similar to what they observed in these experiments. Based on the speed and density of the NKT cells, they calculate that each cell can visit a new hepatocyte every two minutes, and that every hepatocyte is surveyed approximately once every 15 minutes. This is in stark contrast to surveillance in the lymph nodes, in which a typical dendritic cell receives 5,000 visits per hour from its resident T cells, but it may make biological sense given that NKT cells have a much more restricted range than conventional T cells.