23 research outputs found

    A Cis-Regulatory Map of the Drosophila Genome

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    Systematic annotation of gene regulatory elements is a major challenge in genome science. Direct mapping of chromatin modification marks and transcriptional factor binding sites genome-wide1, 2 has successfully identified specific subtypes of regulatory elements3. In Drosophila several pioneering studies have provided genome-wide identification of Polycomb response elements4, chromatin states5, transcription factor binding sites6, 7, 8, 9, RNA polymerase II regulation8 and insulator elements10; however, comprehensive annotation of the regulatory genome remains a significant challenge. Here we describe results from the modENCODE cis-regulatory annotation project. We produced a map of the Drosophila melanogaster regulatory genome on the basis of more than 300 chromatin immunoprecipitation data sets for eight chromatin features, five histone deacetylases and thirty-eight site-specific transcription factors at different stages of development. Using these data we inferred more than 20,000 candidate regulatory elements and validated a subset of predictions for promoters, enhancers and insulators in vivo. We identified also nearly 2,000 genomic regions of dense transcription factor binding associated with chromatin activity and accessibility. We discovered hundreds of new transcription factor co-binding relationships and defined a transcription factor network with over 800 potential regulatory relationships

    BMP signaling components in embryonic transcriptomes of the hover fly Episyrphus balteatus (Syrphidae)

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    <p>Abstract</p> <p>Background</p> <p>In animals, signaling of Bone Morphogenetic Proteins (BMPs) is essential for dorsoventral (DV) patterning of the embryo, but how BMP signaling evolved with changes in embryonic DV differentiation is largely unclear. Based on the extensive knowledge of BMP signaling in <it>Drosophila melanogaster</it>, the morphological diversity of extraembryonic tissues in different fly species provides a comparative system to address this question. The closest relatives of <it>D. melanogaster </it>with clearly distinct DV differentiation are hover flies (Diptera: Syrphidae). The syrphid <it>Episyrphus balteatus </it>is a commercial bio-agent against aphids and has been established as a model organism for developmental studies and chemical ecology. The dorsal blastoderm of <it>E. balteatus </it>gives rise to two extraembryonic tissues (serosa and amnion), whereas in <it>D. melanogaster</it>, the dorsal blastoderm differentiates into a single extraembryonic epithelium (amnioserosa). Recent studies indicate that several BMP signaling components of <it>D. melanogaster</it>, including the BMP ligand Screw (Scw) and other extracellular regulators, evolved in the dipteran lineage through gene duplication and functional divergence. These findings raise the question of whether the complement of BMP signaling components changed with the origin of the amnioserosa.</p> <p>Results</p> <p>To search for BMP signaling components in <it>E. balteatus</it>, we generated and analyzed transcriptomes of freshly laid eggs (0-30 minutes) and late blastoderm to early germband extension stages (3-6 hours) using Roche/454 sequencing. We identified putative <it>E. balteatus </it>orthologues of 43% of all annotated <it>D. melanogaster </it>genes, including the genes of all BMP ligands and other BMP signaling components.</p> <p>Conclusion</p> <p>The diversification of several BMP signaling components in the dipteran linage of <it>D. melanogaster </it>preceded the origin of the amnioserosa.</p> <p>[Transcriptome sequence data from this study have been deposited at the NCBI Sequence Read Archive (SRP005289); individually assembled sequences have been deposited at GenBank (<ext-link ext-link-id="JN006969" ext-link-type="gen">JN006969</ext-link>-<ext-link ext-link-id="JN006986" ext-link-type="gen">JN006986</ext-link>).]</p

    Solidification Modeling of a Spiral Casting to Determine Material Fluidity by DISTRIBUTION OF THIS DOCUMENT IS UNLIMITED Solidification Modeling of a Spiral Casting to Determine Material Fluidity

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    Abstract In casting, fluidity is the measure of the distance a metal can flow in a channel before being stopped by solidification. During mold filling, the metal loses heat to the surrounding mold, thereby cooling and becoming more viscous until the leading portion solidifies and no further flow is possible. A coupled heat-transfer and fluid-flow modeling of a spiral, involving the use of thermophysical properties to determine material fluidity, has been conducted. Fluidity experiments were performed by Caterpillar; several spiral test castings were poured. Simulations of these experiments utilized the Casting Process Simulator (CaPS) software developed at Argonne National Laboratory. Two types of spiral geometries with different assumptions were considered: (1) a two-dimensional laterally stretched spiral and (2) a three-dimensional lateral spiral. The computed extent of mold filling is in good agreement with the experimental results. Time required by the metal/gas interface to attain specific positions in the spiral arm also compares favorably with the experimental results. &apos;The influence of process variables, especially pour time, is discussed. The CaPS software has been used as a computational tool to investigate the validity of the dimensionality assumptions and to evaluate the ability of CaPS to model fluidity adequately. iii Content

    Experiment data report IFA-226 postirradiation examination. [PWR, BWR]

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    IFA-226 contained twelve, mixed plutonium-uranium oxide fuel rods arranged in two, six-rod clusters. The assembly was designed to study fuel-cladding mechanical interaction, fuel thermal response, and fission gas release as a function of fuel density, initial fuel-to-cladding gap, rod power, and burnup. Data were obtained from fuel rod centerline thermocouples, fission gas pressure transducers, and cladding elongation sensors. Results of both nondestructive and destructive examinations are presented. The PIE indicated that one fuel rod failed during service as a result of internal hydriding of the end plug. Circumferential cladding ridges resulting from fuel-cladding interaction were present on all of the rods, with the largest ridges present on the rod with the smallest initial fuel-to-cladding gap. No incipient fuel rod failures were detected
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