53 research outputs found

    Locus specific epigenetic modalities of random allelic expression imbalance

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    Most autosomal genes are thought to be expressed from both alleles, with some notable exceptions, including imprinted genes and genes showing random monoallelic expression (RME). The extent and nature of RME has been the subject of debate. Here we investigate the expression of several candidate RME genes in F1 hybrid mouse cells before and after differentiation, to define how they become persistently, monoallelically expressed. Clonal monoallelic expression is not present in embryonic stem cells, but we observe high frequencies of monoallelism in neuronal progenitor cells by assessing expression status in more than 200 clones. We uncover unforeseen modes of allelic expression that appear to be gene-specific and epigenetically regulated. This non-canonical allelic regulation has important implications for development and disease, including autosomal dominant disorders and opens up therapeutic perspectives

    Current Status of a Model System: The Gene Gp-9 and Its Association with Social Organization in Fire Ants

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    The Gp-9 gene in fire ants represents an important model system for studying the evolution of social organization in insects as well as a rich source of information relevant to other major evolutionary topics. An important feature of this system is that polymorphism in social organization is completely associated with allelic variation at Gp-9, such that single-queen colonies (monogyne form) include only inhabitants bearing B-like alleles while multiple-queen colonies (polygyne form) additionally include inhabitants bearing b-like alleles. A recent study of this system by Leal and Ishida (2008) made two major claims, the validity and significance of which we examine here. After reviewing existing literature, analyzing the methods and results of Leal and Ishida (2008), and generating new data from one of their study sites, we conclude that their claim that polygyny can occur in Solenopsis invicta in the U.S.A. in the absence of expression of the b-like allele Gp-9b is unfounded. Moreover, we argue that available information on insect OBPs (the family of proteins to which GP-9 belongs), on the evolutionary/population genetics of Gp-9, and on pheromonal/behavioral control of fire ant colony queen number fails to support their view that GP-9 plays no role in the chemosensory-mediated communication that underpins regulation of social organization. Our analyses lead us to conclude that there are no new reasons to question the existing consensus view of the Gp-9 system outlined in Gotzek and Ross (2007)

    Expressed sequence tags from Atta laevigata and identification of candidate genes for the control of pest leaf-cutting ants

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    <p>Abstract</p> <p>Background</p> <p>Leafcutters are the highest evolved within Neotropical ants in the tribe Attini and model systems for studying caste formation, labor division and symbiosis with microorganisms. Some species of leafcutters are agricultural pests controlled by chemicals which affect other animals and accumulate in the environment. Aiming to provide genetic basis for the study of leafcutters and for the development of more specific and environmentally friendly methods for the control of pest leafcutters, we generated expressed sequence tag data from <it>Atta laevigata</it>, one of the pest ants with broad geographic distribution in South America.</p> <p>Results</p> <p>The analysis of the expressed sequence tags allowed us to characterize 2,006 unique sequences in <it>Atta laevigata</it>. Sixteen of these genes had a high number of transcripts and are likely positively selected for high level of gene expression, being responsible for three basic biological functions: energy conservation through redox reactions in mitochondria; cytoskeleton and muscle structuring; regulation of gene expression and metabolism. Based on leafcutters lifestyle and reports of genes involved in key processes of other social insects, we identified 146 sequences potential targets for controlling pest leafcutters. The targets are responsible for antixenobiosis, development and longevity, immunity, resistance to pathogens, pheromone function, cell signaling, behavior, polysaccharide metabolism and arginine kynase activity.</p> <p>Conclusion</p> <p>The generation and analysis of expressed sequence tags from <it>Atta laevigata </it>have provided important genetic basis for future studies on the biology of leaf-cutting ants and may contribute to the development of a more specific and environmentally friendly method for the control of agricultural pest leafcutters.</p

    Molecular Variation at a Candidate Gene Implicated in the Regulation of Fire Ant Social Behavior

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    The fire ant Solenopsis invicta and its close relatives display an important social polymorphism involving differences in colony queen number. Colonies are headed by either a single reproductive queen (monogyne form) or multiple queens (polygyne form). This variation in social organization is associated with variation at the gene Gp-9, with monogyne colonies harboring only B-like allelic variants and polygyne colonies always containing b-like variants as well. We describe naturally occurring variation at Gp-9 in fire ants based on 185 full-length sequences, 136 of which were obtained from S. invicta collected over much of its native range. While there is little overall differentiation between most of the numerous alleles observed, a surprising amount is found in the coding regions of the gene, with such substitutions usually causing amino acid replacements. This elevated coding-region variation may result from a lack of negative selection acting to constrain amino acid replacements over much of the protein, different mutation rates or biases in coding and non-coding sequences, negative selection acting with greater strength on non-coding than coding regions, and/or positive selection acting on the protein. Formal selection analyses provide evidence that the latter force played an important role in the basal b-like lineages coincident with the emergence of polygyny. While our data set reveals considerable paraphyly and polyphyly of S. invicta sequences with respect to those of other fire ant species, the b-like alleles of the socially polymorphic species are monophyletic. An expanded analysis of colonies containing alleles of this clade confirmed the invariant link between their presence and expression of polygyny. Finally, our discovery of several unique alleles bearing various combinations of b-like and B-like codons allows us to conclude that no single b-like residue is completely predictive of polygyne behavior and, thus, potentially causally involved in its expression. Rather, all three typical b-like residues appear to be necessary

    The venom composition of the parasitic wasp Chelonus inanitus resolved by combined expressed sequence tags analysis and proteomic approach

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    <p>Abstract</p> <p>Background</p> <p>Parasitic wasps constitute one of the largest group of venomous animals. Although some physiological effects of their venoms are well documented, relatively little is known at the molecular level on the protein composition of these secretions. To identify the majority of the venom proteins of the endoparasitoid wasp <it>Chelonus inanitus </it>(Hymenoptera: Braconidae), we have randomly sequenced 2111 expressed sequence tags (ESTs) from a cDNA library of venom gland. In parallel, proteins from pure venom were separated by gel electrophoresis and individually submitted to a nano-LC-MS/MS analysis allowing comparison of peptides and ESTs sequences.</p> <p>Results</p> <p>About 60% of sequenced ESTs encoded proteins whose presence in venom was attested by mass spectrometry. Most of the remaining ESTs corresponded to gene products likely involved in the transcriptional and translational machinery of venom gland cells. In addition, a small number of transcripts were found to encode proteins that share sequence similarity with well-known venom constituents of social hymenopteran species, such as hyaluronidase-like proteins and an Allergen-5 protein.</p> <p>An overall number of 29 venom proteins could be identified through the combination of ESTs sequencing and proteomic analyses. The most highly redundant set of ESTs encoded a protein that shared sequence similarity with a venom protein of unknown function potentially specific of the <it>Chelonus </it>lineage. Venom components specific to <it>C. inanitus </it>included a C-type lectin domain containing protein, a chemosensory protein-like protein, a protein related to yellow-e3 and ten new proteins which shared no significant sequence similarity with known sequences. In addition, several venom proteins potentially able to interact with chitin were also identified including a chitinase, an imaginal disc growth factor-like protein and two putative mucin-like peritrophins.</p> <p>Conclusions</p> <p>The use of the combined approaches has allowed to discriminate between cellular and truly venom proteins. The venom of <it>C. inanitus </it>appears as a mixture of conserved venom components and of potentially lineage-specific proteins. These new molecular data enrich our knowledge on parasitoid venoms and more generally, might contribute to a better understanding of the evolution and functional diversity of venom proteins within Hymenoptera.</p

    RNA-sequencing elucidates the regulation of behavioural transitions associated with mating in honey bee queens

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    This study was funded by a BBSRC ISIS grant BB/J019453/1, a Royal Holloway Research Strategy Fund Grant, and a Leverhulme Grant F/07537/AK to MJFB. BPO was supported by Australian Research Council Discovery grants DP150100151 and DP120101915. FM was supported by a Marie Curie International Incoming Fellowship FP7-PEOPLE-2013-IIF-625487 to MJFB. We would like to thank Dave Galbraight (Penn State) and Alberto Paccanaro (RHUL) for support with analysis of RNAseq data and four anonymous reviewers for providing thoughtful insights that helped to improve the manuscript.Peer reviewedPublisher PD

    DĂ©termination Ă©lectrochimique de l'Ă©paisseur des biofilms dans les circuits d'eau

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    MatĂ©riaux & Techniques 95, 67-67 (2007) - Erratum : DĂ©termination Ă©lectrochimique de l'Ă©paisseur des biofilms dans les circuits d'eauN° Hors SĂ©rie : VIII Ăšme Forum de BiodĂ©tĂ©rioration des MatĂ©riauxInternational audienceElectrochemical determination of biofilm thickness in water systems.Biofilms are growing on the internal wall of the water pipelines, this is a constantproblem of health risk. The legionella which proliferate in the warm waters networks andin cooling towers, are at the origin of more than 1000 cases of Legionnaire’s disease peryear in France during the last three years, the death rate being about 14%. To control thisbacterial development, a better understanding of biofilms ecology is necessary, in particulartheir growth and their composition. In this purpose, three working years of collaborationbetween the company Henkel Concorde and 2 CNRS research teams (UMR 6008 and UPR 15)allowed to develop a tool able to measure the biofilm thickness. On laboratory pilots andin industrial site, this biofilm thickness measurement showed a very acceptable reliabilityand sensitivity to follow the behaviour of a biofilm in a water circuit and to evaluate theefficiency of the treatments (dispersing, biocide) which are applied. The use of this toolallows to optimize the applied treatments (nature, dose, frequency of injection) and leadsto a strong reduction of the sessile biomass. Thanks to this sensor the cleanliness of watercircuits could be maintained with a better efficiency and thus a greater control of thelegionella risk could be obtained.La croissance de biofilms sur les parois des rĂ©seaux et des circuits d’eaux est unproblĂšme rĂ©current en terme de santĂ© publique. Les lĂ©gionelles qui se dĂ©veloppent dans lesrĂ©seaux d’eaux chaudes et les tours aĂ©rorĂ©frigĂ©rantes ont Ă©tĂ© Ă  l’origine de plus de 1000 casannuels de lĂ©gionellose en France au cours des 3 derniĂšres annĂ©es, la lĂ©talitĂ© Ă©tant d’environ14 %. Pour maĂźtriser ce dĂ©veloppement bactĂ©rien, il est nĂ©cessaire de possĂ©der unemeilleure comprĂ©hension des biofilms, de leur croissance et de leur composition. Dans cebut, trois annĂ©es de travail de collaboration entre la sociĂ©tĂ© Henkel Concorde et 2 Ă©quipesCNRS (UMR 6008 et UPR 15) ont permis de dĂ©velopper un outil de dĂ©termination de l’épaisseurmoyenne du biofilm. Sur des unitĂ©s pilote en laboratoire et sur site industriel, cettemesure de l’épaisseur du biofilm s’est rĂ©vĂ©lĂ©e suffisamment prĂ©cise et sensible pour suivrel’évolution de la formation d’un biofilm dans un circuit d’eau et pour dĂ©terminer l’efficacitĂ©des traitements appliquĂ©s. L’utilisation de cet outil de surveillance a permis d’optimiserles traitements appliquĂ©s (nature, dose, frĂ©quence d’injection) et conduit Ă  une rĂ©ductionsignificative des biomasses fixĂ©es, au maintien de la propretĂ© des circuits et donc Ă  unemaĂźtrise accrue du risque lĂ©gionelle
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