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Not just another genome
BMC Biology volume 9, Article number: 8 (2011)
Sequence analysis of the Daphnia pulex genome holds some surprises that could not have been anticipated from what was learned so far from other arthropod genomes. It establishes Daphnia as an eco-genetical model organism par excellence.
Genome of an aquatic sensor
One of my first courses in biology included an experiment in which we subjected Daphnia populations in glass beakers to different concentrations of a water pollutant and counted the fraction that stopped swimming around. This is still a very common test to monitor water quality and it is said to be more sensitive than any conventional chemical analysis. It reflects the fact that Daphnia plays a key role in fresh water ecology (Figure 1), not only for testing but also as a central component of nutrient cycles. In a typical lake in spring, Daphnia lives in paradise with food in the form of algae swimming around it ready to be collected at will. But no paradise lasts for ever. As the Daphnia population grows, algae become increasingly rare to the point of almost complete disappearance, leading to a short phase in the yearly cycle of a lake in which the water becomes crystal clear . Daphnia itself increasingly becomes a victim of predators during the yearly cycle and, although it starts to develop defenses , its population shrinks such that the algae can become more abundant again. The nutrient flux that is involved in this cycle is enormous and drives the whole ecology of the lake. But how can a genome sequence help to learn more about this ecology? The Daphnia genome  turns out to hold a large number of genes which were previously not known and which, excitingly, are likely to have a specific role in the interaction with its environment. The Daphnia genome may thus become a Rosetta stone for studying the genetic repertoire of fresh water ecology.
An abundance of newly evolved genes
Could one have expected that specific genes have evolved to cope with particular environmental challenges? A common notion in current evolutionary biology is that novelty arises out of the duplication and redeployment of ancient genes or protein domains in new regulatory pathways. This would not leave much room for the evolution of completely new genes. However, it is well known that every major evolutionary lineage contains genes that are only found in this lineage and can therefore be expected to have newly evolved . There are also good reasons to speculate that they have lineage specific functions  that likely include some that are relevant for environmental interactions. And it is now clear that Daphnia has a particularly large number of newly evolved genes - roughly a third of all that were identified in its genome so far.
One focus of the genome paper  is therefore to trace the origin of this novel gene repertoire. A hallmark of these genes is that they occur in gene families - that is, they have arisen, duplicated and diverged within the genome. The authors find a generally higher propensity for gene duplications and retention in Daphnia compared to other organisms and this includes not only the unknown genes, but also well known ones. For example, the expansion of photoresponsive gene families such as cryptochromes, opsins, and G proteins may play a role in coping with the complex light regime in aquatic environments ; or multiple copies of insulin receptor genes with special structures and differential expression might contribute to the plasticity in body size, as suggested in a companion paper . Of course, gene duplication on its own does not create much novelty, but these duplicates diverge over time, with respect to both their regulation and their sequences. And there is abundant evidence for concerted evolution among duplicates , which may create an additional level of evolutionary dynamics . Interestingly, in Daphnia there is also a large fraction of very recent duplicates that show differential expression to environmental challenges, indicating that these duplicates have very quickly become involved in specific adaptations . Again, one has to emphasize that this includes homologues of both previously known and unknown genes; thus, regulatory and protein evolution appear to take place concurrently. In fact, this tendency was already found in a previous study that aimed to identify cadmium-responsive genes . Among the genes that were differentially regulated in response to varying doses of cadmium were metallothionein genes with highly diverged protein sequences, but with consensus metal-responsive elements in their promotors.
A clear case for an adaptive role of duplication and selective retention of duplicates comes from the analysis of genes involved in known metabolic pathways. Half of the expanded metabolic genes were found to belong to a subset of seven distinct pathways and the expression patterns of these genes co-diverge according to their pathway, not to their evolutionary history . But also the non-classifiable genes show expression characteristics that suggest a direct connection to the environment. When differential expression with respect to different environmental conditions, such as exposure to metals or to predators, was analyzed, twice as many of them were responsive compared to the set of known genes . Most intriguingly, there is apparently a further set of transcripts that are responsive to the environment, but whose structure could not yet be described since they were not found in EST libraries and did not fit the gene annotation models. They were identified by hybridization of RNA to whole genome tiling arrays, which revealed almost 35,000 additional transcriptionally active regions in the genome. These were not captured by other identification methods, but likely represent exons of an unknown number of additional genes  that await structural and functional characterization.
Life cycle plasticity may facilitate rapid evolution
Why is Daphnia so particularly amenable to developing an eco-responsive gene repertoire? On the one hand it is known that positive selection is much more efficient in large populations, since even genes or alleles that provide only a very small advantage are retained in the population rather than being lost by drift. However, large population sizes are also found in the insects for which full genome sequences are available - and they show no indication of a particularly strong genomic response to the environment. The explanation may lie with some additional peculiarities of population genetics shown by Daphnia. It can switch between parthenogenetic and sexual reproduction and it can produce resting stages that can survive for decades . Since parthenogenetic reproduction is numerically twice as efficient as sexual reproduction, Daphnia takes advantage of this in spring when a particularly fast population expansion is possible. This leads to a rapid amplification of clones that may have only a minimal advantage over their conspecifics. Of course, once the environment changes, the advantage of such clones may falter quickly, but this is the point where they can go into a sexual cycle and can produce special eggs that are protected by a cuticular structure that allows them to survive in the mud . Thus, all lakes harbor a genetic reservoir of resting eggs derived from animals that had a particular advantage at a previous time. Genes or alleles that were once successful can thus be preserved, even if the environmental conditions are temporarily changed. An explicit evolutionary theory that models the long-term adaptive consequences of such complex life cycles is still missing but, at least intuitively, it would seem that this adds to the evolutionary dynamics that have led to the special gene repertoire of Daphnia.
Because of these peculiarities, Daphnia should now also become a prime model for studying the evolution and the role of sex. One of the companion papers has indeed already specifically addressed such issues by looking at the evolutionary dynamics of transposons in Daphnia . These authors identified the major transposon families in the Daphnia genome and found active copies for most of them. Six of these were then studied in lines where sex was either promoted or inhibited. The data indicate that sexual reproduction is indeed a major factor to keep the elements under control. This effect could at least partially compensate for the short-term cost of sex and thus explain why sexual reproduction is maintained . Intriguingly, a previous study had suggested that sexual and parthenogenetic reproduction makes use of the same set of meiosis related genes and that an expansion of this gene complement may have helped to develop the parthenogenetic life cycle .
Thus, both the ecological relevance and the evolutionary dynamics of Daphnia populations are bound to attract general attention to Daphnia as a new model system in genetics. Duly, it is already listed among the small select group of model organisms for biomedical research at the NIH . The current genome paper focuses on D. pulex but another species of the genus, Daphnia magna, has an equally long history in ecological research and efforts to elucidate its genome are underway as well . These developments are bound to fuel the newly emerging discipline of ecological genomics , which has so far been one of the last black boxes of genetic research.
Lampert W: Daphnia: model herbivore, predator and prey. Polish J Ecol. 2006, 54: 607-620.
Tollrian R, Leese F: Ecological genomics: steps towards unraveling the genetic basis of inducible defenses in Daphnia. BMC Biol. 2010, 8: 51-10.1186/1741-7007-8-51.
Colbourne JK, Pfender ME, Gilbert D, Thomas WK, Tucker A, Oakley TH, Tokishita S, Aerts A, Arnold GJ, Basu MK, Bauer DJ, Caceres CE, Carmel L, Casola C, Choi JH, Detter JC, Dong Q, Dusheyko S, Eads BD, Frohlich T, Geiler-Samerotte KA, Gerlach D, Hatcher P, Jogdeo S, Krijgsveld J, Kriventseva EV, Kultz D, Laforsch C, Lindquist E, Lopez J, et al: The ecoresponsive genome of Daphnia pulex. Science. 2011, 331: 555-561. 10.1126/science.1197761.
Khalturin K, Hemmrich G, Fraune S, Augustin R, Bosch TC: More than just orphans: are taxonomically-restricted genes important in evolution?. Trends Genet. 2009, 25: 404-413. 10.1016/j.tig.2009.07.006.
Boucher P, Ditlecadet D, Dubé C, Dufresne F: Unusual duplication of the insulin-like receptor in the crustacean Daphnia pulex. BMC Evol Biol. 2010, 10: 305-10.1186/1471-2148-10-305.
Dover GA: Evolution of genetic redundancy for advanced players. Curr Opin Genet Dev. 1993, 3: 902-910. 10.1016/0959-437X(93)90012-E.
Shaw JR, Colbourne JK, Davey JC, Glaholt SP, Hampton TH, Chen CY, Folt CL, Hamilton JW: Gene response profiles for Daphnia pulex exposed to the environmental stressor cadmium reveals novel crustacean metallothioneins. BMC Genomics. 2007, 8: 477-10.1186/1471-2164-8-477.
Schaack s, Choi E, Lynch M, Pritham EJ: DNA transposons and the role of recombination in mutation accumulation in Daphnia pulex. Genome Biol. 2010, 11: R46-10.1186/gb-2010-11-4-r46.
Schurko AM, Logsdon JM, Eads BD: Meiosis genes in Daphnia pulex and the role of parthenogenesis in genome evolution. BMC Evol Biol. 2009, 9: 78-10.1186/1471-2148-9-78.
Model Organisms for Biomedical Research. [http://www.nih.gov/science/models/]
Routtu J, Jansen B, Colson I, De Meester L, Ebert D: The first-generation Daphnia magna linkage map. BMC Genomics. 2010, 11: 508-10.1186/1471-2164-11-508.
Renn SC, Siemens DH: Ecological genomics - changing perspectives on Darwin's basic concerns. Mol Ecol. 2010, 19: 3025-3030. 10.1111/j.1365-294X.2010.04743.x.
Daphnia: Development of a Model Organism in Ecology and Evolution. Excellence in Ecology. Edited by: Kinne O. 2011, International Ecology Institute, Oldendorf/Luhe, Book 21
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Tautz, D. Not just another genome. BMC Biol 9, 8 (2011). https://0-doi-org.brum.beds.ac.uk/10.1186/1741-7007-9-8
- Sexual Reproduction
- Gene Repertoire
- Daphnia Population
- Insulin Receptor Gene
- Parthenogenetic Reproduction