28 research outputs found
Zombi: A phylogenetic simulator of trees, genomes and sequences that accounts for dead lineages
International audienceHere we present Zombi, a tool to simulate the evolution of species, genomes and sequences in silico, that considers for the first time the evolution of genomes in extinct lineages. It also incorporates various features that have not to date been combined in a single simulator, such as the possibility of generating species trees with a pre-defined variation of speciation and extinction rates through time, simulating explicitly intergenic sequences of variable length and outputting gene tree - species tree reconciliations
State tomography for two qubits using reduced densities
The optimal state determination (or tomography) is studied for a composite
system of two qubits when measurements can be performed on one of the qubits
and interactions of the two qubits can be implemented. The goal is to minimize
the number of interactions to be used. The algebraic method applied in the
paper leads to an extension of the concept of mutually unbiased measurements.Comment: 8 pages LATE
Prioritization of fish communities with a view to conservation and restoration on a large scale European basin, the Loire (France)
The hierarchical organization of important sites for the conservation or the
restoration of fish communities is a great challenge for managers, especially because of
financial or time constraints. In this perspective, we developed a methodology, which is
easy to implement in different locations. Based on the fish assemblage characteristics of
the Loire basin (France), we created a synthetic conservation value index including the
rarity, the conservation status and the species origin. The relationship between this new
synthetic index and the Fish-Based Index allowed us to establish a classification protocol
of the sites along the Loire including fish assemblages to be restored or conserved. Sites
presenting disturbed fish assemblages, a low rarity index, few threatened species, and a
high proportion of non-native species were considered as important for the restoration of
fish biodiversity. These sites were found mainly in areas where the assemblages are
typical of the bream zone, e.g. with a higher number of eurytopic and limnophilic
species. On the contrary, important sites for conservation were defined as having an
important conservation potential (high RI, a lot of threatened species, and few nonnatives
fish species) and an undisturbed fish assemblage similar to the expected community
if habitats are undisturbed. Important sites for conservation were found in the
Loire basinâs medium reaches which host assemblages typical for the grayling and the
barbell zones, e.g. with a higher number of rheophilic species. The synthetic conservation value index could be adapted and completed with other criteria according to
management priorities and capacities
Megaphylogeny resolves global patterns of mushroom evolution
Mushroom-forming fungi (Agaricomycetes) have the greatest morphological diversity and complexity of any group of fungi. They have radiated into most niches and fulfil diverse roles in the ecosystem, including wood decomposers, pathogens or mycorrhizal mutualists. Despite the importance of mushroom-forming fungi, large-scale patterns of their evolutionary history are poorly known, in part due to the lack of a comprehensive and dated molecular phylogeny. Here, using multigene and genome-based data, we assemble a 5,284-species phylogenetic tree and infer ages and broad patterns of speciation/extinction and morphological innovation in mushroom-forming fungi. Agaricomycetes started a rapid class-wide radiation in the Jurassic, coinciding with the spread of (sub)tropical coniferous forests and a warming climate. A possible mass extinction, several clade-specific adaptive radiations and morphological diversification of fruiting bodies followed during the Cretaceous and the Paleogene, convergently giving rise to the classic toadstool morphology, with a cap, stalk and gills (pileate-stipitate morphology). This morphology is associated with increased rates of lineage diversification, suggesting it represents a key innovation in the evolution of mushroom-forming fungi. The increase in mushroom diversity started during the Mesozoic-Cenozoic radiation event, an era of humid climate when terrestrial communities dominated by gymnosperms and reptiles were also expanding.Fil: Varga, Torda. Hungarian Academy Of Sciences; HungrĂaFil: KrizsĂĄn, Krisztina. Hungarian Academy Of Sciences; HungrĂaFil: Földi, Csenge. Hungarian Academy Of Sciences; HungrĂaFil: Dima, BĂĄlint. Eötvös LorĂĄnd University; HungrĂaFil: SĂĄnchez-GarcĂa, Marisol. Clark University; Estados UnidosFil: Lechner, Bernardo Ernesto. Consejo Nacional de Investigaciones CientĂficas y TĂ©cnicas. Oficina de CoordinaciĂłn Administrativa Ciudad Universitaria. Instituto de MicologĂa y BotĂĄnica. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de MicologĂa y BotĂĄnica; ArgentinaFil: SĂĄnchez-RamĂrez, Santiago. University of Toronto; CanadĂĄFil: Szöllosi, Gergely J.. Eötvös LorĂĄnd University; HungrĂaFil: SzarkĂĄndi, JĂĄnos G.. University Of Szeged; HungrĂaFil: Papp, Viktor. Szent IstvĂĄn University; HungrĂaFil: Albert, LĂĄszlĂł. Hungarian Mycological Society; HungrĂaFil: Andreopoulos, William. United States Department Of Energy. Joint Genome Institute; Estados UnidosFil: Angelini, Claudio. Jardin Botanico Nacional Ma. Moscoso; RepĂșblica DominicanaFil: AntonĂn, VladimĂr. Moravian Museum; RepĂșblica ChecaFil: Barry, Kerrie W.. United States Department Of Energy. Joint Genome Institute; Estados UnidosFil: Bougher, Neale L.. Western Australian Herbarium; AustraliaFil: Buchanan, Peter. Manaaki Whenua-landcare Research; Nueva ZelandaFil: Buyck, Bart. MusĂ©um National d'Histoire Naturelle; FranciaFil: Bense, ViktĂłria. Hungarian Academy Of Sciences; HungrĂaFil: Catcheside, Pam. State Herbarium Of South Australia; AustraliaFil: Chovatia, Mansi. United States Department Of Energy. Joint Genome Institute; Estados UnidosFil: Cooper, Jerry. Manaaki Whenua-landcare Research; Nueva ZelandaFil: DĂ€mon, Wolfgang. Oberfeldstrasse 9; AustriaFil: Desjardin, Dennis. San Francisco State University; Estados UnidosFil: Finy, PĂ©ter. Zsombolyai U. 56.; HungrĂaFil: Geml, JĂłzsef. Naturalis Biodiversity Center; PaĂses BajosFil: Haridas, Sajeet. United States Department Of Energy. Joint Genome Institute; Estados UnidosFil: Hughes, Karen. University of Tennessee; Estados UnidosFil: Justo, Alfredo. Clark University; Estados UnidosFil: Karasinski, Dariusz. Polish Academy of Sciences; Poloni
Detection of human neutrophil elastase (HNE) on wound dressings as marker of inflammation
Chronic wound fluids have elevated concentration of human neutrophil elastase (HNE) which can be used as inflammation/infection marker. Our goal is to develop functional materials for fast diagnosis of wound inflammation/infection by using HNE as a specific marker. For that, fluorogenic peptides with a HNE-specific cleavage sequence were incorporated into traditional textile dressings, to allow real-time detection of the wound status. Two different fluorogenic approaches were studied in terms of intensity of the signal generated upon HNE addition: a fluorophore 7-amino-4-trifluormethylcoumarin (AFC) conjugated to a HNE-specific peptide and two fluorophore/quencher pairs (FAM/Dabcyl and EDANS/Dabcyl) coupled to a similar peptide as a Förster resonance energy transfer (FRET) strategy. Also, two immobilization methods were tested: sonochemistry immobilization onto a cotton bandage and glutaraldehyde (GTA)-assisted chemical crosslinking onto a polyamide dressing. The immobilized fluorogenic AFC peptide showed an intense fluorescence emission in the presence of HNE. HNE also induced an enhanced fluorescent signal with the EDANS/Dabcyl FRET peptide which showed to be a more sensitive and effective strategy than the AFC peptide. However, its chemical immobilization onto the polyamide dressing greatly decreased its detection, mainly due to the more difficult access of the enzyme to the cleavage sequence of the immobilized peptide. After optimization of the in situ immobilization, it will be possible to use these fluorescence-functionalized dressings for an effective and specific monitoring of chronic wounds by simply using a portable ultraviolet (UV) light source. We envision that the development of this point-of-care medical device for wound control will have a great impact on patients life quality and reduction of costs on health care system.This study was funded by the European project InFact-Functional materials for fast diagnosis of wound infection (FP7-NMP-2013-SME-7-grant agreement no. 604278). The work done at Centre of Biological Engineering (CEB) was also supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit, COMPETE 2020 (POCI-01-0145-FEDER-006684) and BioTecNorte operation (NORTE-01-0145-FEDER-000004) funded by European Regional Development Fund under the scope of Norte 2020-Programa Operacional Regional do Norte
Ancient horizontal gene transfer and the last common ancestors
Background
The genomic history of prokaryotic organismal lineages is marked by extensive horizontal gene transfer (HGT) between groups of organisms at all taxonomic levels. These HGT events have played an essential role in the origin and distribution of biological innovations. Analyses of ancient gene families show that HGT existed in the distant past, even at the time of the organismal last universal common ancestor (LUCA). Most gene transfers originated in lineages that have since gone extinct. Therefore, one cannot assume that the last common ancestors of each gene were all present in the same cell representing the cellular ancestor of all extant life.
Results
Organisms existing as part of a diverse ecosystem at the time of LUCA likely shared genetic material between lineages. If these other lineages persisted for some time, HGT with the descendants of LUCA could have continued into the bacterial and archaeal lineages. Phylogenetic analyses of aminoacyl-tRNA synthetase protein families support the hypothesis that the molecular common ancestors of the most ancient gene families did not all coincide in space and time. This is most apparent in the evolutionary histories of seryl-tRNA synthetase and threonyl-tRNA synthetase protein families, each containing highly divergent ârareâ forms, as well as the sparse phylogenetic distributions of pyrrolysyl-tRNA synthetase, and the bacterial heterodimeric form of glycyl-tRNA synthetase. These topologies and phyletic distributions are consistent with horizontal transfers from ancient, likely extinct branches of the tree of life.
Conclusions
Of all the organisms that may have existed at the time of LUCA, by definition only one lineage is survived by known progeny; however, this lineage retains a genomic record of heterogeneous genetic origins. The evolutionary histories of aminoacyl-tRNA synthetases (aaRS) are especially informative in detecting this signal, as they perform primordial biological functions, have undergone several ancient HGT events, and contain many sites with low substitution rates allowing deep phylogenetic reconstruction. We conclude that some aaRS families contain groups that diverge before LUCA. We propose that these ancient gene variants be described by the term âhypnologsâ, reflecting their ancient, reticulate origin from a time in life history that has been all but erasedâ.National Science Foundation (U.S.) (Grant DEB 0830024)Exobiology Program (U.S.) (Grant NNX10AR85G)United States. National Aeronautics and Space Administration (Postdoctoral Program
Lateral Gene Transfer from the Dead.
International audienceIn phylogenetic studies, the evolution of molecular sequences is assumed to have taken place along the phylogeny traced by the ancestors of extant species. In the presence of lateral gene transfer (LGT), however, this may not be the case, because the species lineage from which a gene was transferred may have gone extinct or not have been sampled. Because it is not feasible to specify or reconstruct the complete phylogeny of all species, we must describe the evolution of genes outside the represented phylogeny by modelling the speciation dynamics that gave rise to the complete phylogeny. We demonstrate that if the number of sampled species is small compared to the total number of existing species, the overwhelming majority of gene transfers involve speciation to, and evolution along extinct or unsampled lineages. We show that the evolution of genes along extinct or unsampled lineages can to good approximation be treated as those of independently evolving lineages described by a few global parameters. Using this result, we derive an algorithm to calculate the probability of a gene tree and recover the maximum likelihood reconciliation given the phylogeny of the sampled species. Examining 473 near universal gene families from 36 cyanobacteria, we find that nearly a third of transfer events - 28% - appear to have topological signatures of evolution along extinct species, but only approximately 6% of transfers trace their ancestry to before the common ancestor of the sampled cyanobacteria
Dating with transfers
National audienceTo reconstruct the timing of the diversification of life on Earth, biologists combine fossil evidence with inferences drawn from the comparison of genome sequences. These inferences are based on the molecular clock or on a softer version of it, the relaxed molecular clock. This approach consists of estimating the divergence between sequences and then, assuming that mutations occur clockwise , trying to determine the age of the ancestral sequence. This method can be refined by using diverse models that relax the hypothesis of constant pace of evolution and consider that sequences can evolve at different speeds. Some models assume that these rates of evolution are independent along the different branches of the tree relating the different sequences of DNA; some others consider that the rates are correlated among related branches, so the rate of a given branch is inherited to some extent from the parental one. Which is of these methods perform best is still heavily debated. In spite of the sophistication of the different models, calculating these rates is not a trivial problem and the best estimates of divergence time have usually very wide confidence intervals. To overcome this problem scientists can use fossils, that can be independently dated using methods such as stratigraphy or radiometry. Fossils are useful because they provide external information that can be used to constrain the positions of the nodes in a species tree, improving the accuracy of the estimates of the molecular clock. Combining relaxed molecular clock estimates and fossil is in active field of research in phylogenetics [1]. However, fossils are extremely scarce in the geological record. For about 80 % of the history of life, all organisms were unicellular, which means that finding fossils becomes an almost impossible task. Bones and hard shells are easy to be preserved but they just became frequent after the Cambrian explosion, when all the major animal clades appear at sudden. Before that Earth was dominated by bacteria and to a minor extent, small eukaryotes. These organisms are extremely small organisms with no hard parts that can fossilize easily. On top of that, for the few existent fossils we have there is very little certainty about the clades to which they belong, since morphological features cannot be used to place them in a phylogenetic tree. This means that if we are interested in studying what happened in the distant past, we have very little help coming from fossils and we must rely almost exclusively in the information conveyed by the DNA. As we previously stated, this is a hard problem since the estimates of the molecular clock can vary widely. We need accurate calculations if we want to know for example when did Eukaryotes diversify or when did cyanobacteria appear on Earth. To overcome these problems, we propose a new method of dating, based on the DNA sequence complementary to the molecular clock. Lateral gene transfer (LGT) is a common and almost universal phenomenon in nature, where different species (sometimes even species belonging to different domains) exchange genes. This can be detected using differences between species trees and gene trees. We do this using ALE, a method to reconcile species trees and gene trees that allows