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1“…We studied variation in alternative splicing among four different temperatures, 13, 18, 23, and 29°, in two Drosophila melanogaster genotypes. We show plasticity of alternative splicing with up to 10% of the expressed genes being differentially spliced between the most extreme temperatures for a given genotype. …”
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2por Debat, Vincent, Bloyer, Sébastien, Faradji, Floria, Gidaszewski, Nelly, Navarro, Nicolas, Orozco-terWengel, Pablo, Ribeiro, Valérie, Schlötterer, Christian, Deutsch, Jean S., Peronnet, Frédérique“…We observed that Drosophila melanogaster overexpressing Cyclin G (CycG) exhibit wing asymmetry clearly detectable by sight. …”
Publicado 2011
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3Evolution of Eye Morphology and Rhodopsin Expression in the Drosophila melanogaster Species Subgrouppor Posnien, Nico, Hopfen, Corinna, Hilbrant, Maarten, Ramos-Womack, Margarita, Murat, Sophie, Schönauer, Anna, Herbert, Samantha L., Nunes, Maria D. S., Arif, Saad, Breuker, Casper J., Schlötterer, Christian, Mitteroecker, Philipp, McGregor, Alistair P.Enlace del recurso
Publicado 2012
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5“…Here, we studied how the interplay of genetic and environmental variation affects gene expression by exposing Drosophila melanogaster strains to four different developmental temperatures. …”
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6por Posnien, Nico, Hopfen, Corinna, Hilbrant, Maarten, Ramos-Womack, Margarita, Murat, Sophie, Schönauer, Anna, Herbert, Samantha L., Nunes, Maria D. S., Arif, Saad, Breuker, Casper J., Schlötterer, Christian, Mitteroecker, Philipp, McGregor, Alistair P.Enlace del recurso
Publicado 2012
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7por Arif, Saad, Murat, Sophie, Almudi, Isabel, Nunes, Maria D.S., Bortolamiol-Becet, Diane, McGregor, Naomi S., Currie, James M.S., Hughes, Harri, Ronshaugen, Matthew, Sucena, Élio, Lai, Eric C., Schlötterer, Christian, McGregor, Alistair P.“…Therefore, the contribution of miRNAs to evolutionary change remains unknown [1, 4]. Drosophila melanogaster subgroup species display a portion of trichome-free cuticle on the femur of the second leg called the “naked valley.” …”
Publicado 2013
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8“…Wolbachia are maternally inherited bacteria, which typically spread in the host population by inducing cytoplasmic incompatibility (CI). In Drosophila melanogaster, Wolbachia is quite common but CI is variable, with most of the studies reporting low levels of CI. …”
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9por Bastide, Héloïse, Betancourt, Andrea, Nolte, Viola, Tobler, Raymond, Stöbe, Petra, Futschik, Andreas, Schlötterer, Christian“…Here, we use a replicated genome-wide association approach (Pool-GWAS) to fine-scale map genomic regions contributing to natural variation in female abdominal pigmentation in Drosophila melanogaster, a trait that is highly variable in natural populations and highly heritable in the laboratory. …”
Publicado 2013
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10“…We address this problem in two complementary analyses of three replicate Drosophila melanogaster populations evolving to a new hot temperature environment for almost 70 generations. …”
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11“…Thermal stress is a pervasive selective agent in natural populations that impacts organismal growth, survival, and reproduction. Drosophila melanogaster exhibits a variety of putatively adaptive phenotypic responses to thermal stress in natural and experimental settings; however, accompanying assessments of fitness are typically lacking. …”
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12por Fabian, Daniel K, Kapun, Martin, Nolte, Viola, Kofler, Robert, Schmidt, Paul S, Schlötterer, Christian, Flatt, Thomas“…Understanding the genetic underpinnings of adaptive change is a fundamental but largely unresolved problem in evolutionary biology. Drosophila melanogaster, an ancestrally tropical insect that has spread to temperate regions and become cosmopolitan, offers a powerful opportunity for identifying the molecular polymorphisms underlying clinal adaptation. …”
Publicado 2012
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13por Versace, Elisabetta, Nolte, Viola, Pandey, Ram Vinay, Tobler, Ray, Schlötterer, Christian“…We present experimental evolution as a new approach to study Wolbachia infection dynamics in replicate populations exposed to a controlled environment. A natural Drosophila melanogaster population infected with strains of Wolbachia belonging to different clades evolved in two laboratory environments (hot and cold) for 1.5 years. …”
Publicado 2014
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14“…Traits with a common genetic basis frequently display correlated phenotypic responses to selection or environmental conditions. In Drosophila melanogaster, pigmentation of the abdomen and a trident‐shaped region on the thorax are genetically correlated. …”
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15“…Here, we address this question by studying the dynamics of Wolbachia, a well-studied endosymbiont of Drosophila melanogaster. D. melanogaster populations infected with 13 different Wolbachia strains were exposed to novel hot and cold laboratory environments for up to 180 generations. …”
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16“…Rather than starting from many founders, we only use two inbred Drosophila melanogaster strains and expose them to a very extreme, hot temperature environment (29 °C). …”
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17por Kapun, Martin, van Schalkwyk, Hester, McAllister, Bryant, Flatt, Thomas, Schlötterer, Christian“…Here, we have developed a new set of diagnostic marker SNPs for seven cosmopolitan inversions in Drosophila melanogaster that can be used to infer inversion frequencies from Pool-Seq data. …”
Publicado 2014
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19“…We apply this method to data from a natural Drosophila melanogaster population from Portugal. Consistent with previous reports, we show that low recombining genomic regions harbor more TE insertions and maintain insertions at higher frequencies than do high recombining regions. …”
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20“…Here, we address this problem, using a replicated pooled genome-wide association study approach (Pool-GWAS) to compare the genetic basis of variation in abdominal pigmentation in female European and South African Drosophila melanogaster. We find that, in both the European and the South African flies, variants near the tan and bric-à-brac 1 (bab1) genes are most strongly associated with pigmentation. …”
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