4 research outputs found
Competencias en argumentaci贸n y uso de pruebas : 10 ideas clave
Incluye glosarioEl libro trata en las 5 primeras ideas la caracterizaci贸n y elementos de los argumentos y el uso de las pruebas. En las 5 siguientes la argumentaci贸n en diferentes contextos: explicaciones causales, cuestiones sociocient铆ficas, argumentaci贸n oral y escrita y c贸mo promoverla y evaluarla en el aula. El libro esta dirigido al profesorado que se centra en que los alumnos razonen las respuestas.Catalu帽aBiblioteca de Educaci贸n del Ministerio de Educaci贸n, Cultura y Deporte; Calle San Agust铆n 5 -3 Planta; 28014 Madrid; Tel. +34917748000; [email protected]
Pine weevils modulate defensive behaviour in response to parasites of differing virulence
Grooming and avoidance of contaminated areas are among the behavioural defences employed by
animals against parasites. Antiparasite defence behaviour is costly in terms of time, energy and/or food
foregone and therefore animals are expected to modulate their defences depending on the risk of attack
and/or the severity of the symptoms caused.We tested the hypothesis that an insect host invests more in
defence against more virulent (more likely to cause death) than less virulent parasites. We tested
avoidance and grooming of adult pine weevils, Hylobius abietis, in response to infective juveniles of two
species of entomopathogenic nematodes, the more virulent Steinernema carpocapsae and less virulent
Heterorhabditis downesi. Weevils avoided feeding on a substrate contaminated with S. carpocapsae but
not H. downesi. Weevils also groomed more when their bodies were contaminated with S. carpocapsae
than either H. downesi or water. We also made direct observations of nematodes on weevils. When equal
numbers of nematodes were applied to weevils more S. carpocapsae than H. downesi moved actively on
the weevil鈥檚 cuticle. Thus, the differential response of weevils to the two nematode species can be
explained by the weevils detecting the more aggressive behaviour of S. carpocapsae than H. downesi,
which corresponds to a higher probability of death
A genome-wide screen for dendritically localized RNAs identifies genes required for dendrite morphogenesis.
Localizing messenger RNAs at specific subcellular sites is a conserved mechanism for targeting the synthesis of cytoplasmic proteins to distinct subcellular domains, thereby generating asymmetric protein distributions necessary for cellular and developmental polarity. However, the full range of transcripts that are asymmetrically distributed in specialized cell types and the significance of their localization, especially in the nervous system, are not known. We used the EP-MS2 method, which combines EP transposon insertion with the MS2/MCP in vivo fluorescent labeling system to screen for novel localized transcripts in polarized cells, focusing on the highly branched Drosophila class IV dendritic arborization neurons. Of a total of 541 lines screened, we identified 55 EP-MS2 insertions producing transcripts that were enriched in neuronal processes, particularly in dendrites. The 47 genes identified by these insertions encode molecularly diverse proteins and are enriched for genes that function in neuronal development and physiology. RNAi-mediated knockdown confirmed roles for many of the candidate genes in dendrite morphogenesis. We propose that the transport of mRNAs encoded by these genes into the dendrites allows their expression to be regulated on a local scale during the dynamic developmental processes of dendrite outgrowth, branching, and/or remodeling
A Genome-Wide Screen for Dendritically Localized RNAs Identifies Genes Required for Dendrite Morphogenesis
Localizing messenger RNAs at specific subcellular sites is a conserved mechanism for targeting the synthesis of cytoplasmic proteins to distinct subcellular domains, thereby generating asymmetric protein distributions necessary for cellular and developmental polarity. However, the full range of transcripts that are asymmetrically distributed in specialized cell types and the significance of their localization, especially in the nervous system, are not known. We used the EP-MS2 method, which combines EP transposon insertion with the MS2/MCP in vivo fluorescent labeling system to screen for novel localized transcripts in polarized cells, focusing on the highly branched Drosophila class IV dendritic arborization neurons. Of a total of 541 lines screened, we identified 55 EP-MS2 insertions producing transcripts that were enriched in neuronal processes, particularly in dendrites. The 47 genes identified by these insertions encode molecularly diverse proteins and are enriched for genes that function in neuronal development and physiology. RNAi-mediated knockdown confirmed roles for many of the candidate genes in dendrite morphogenesis. We propose that the transport of mRNAs encoded by these genes into the dendrites allows their expression to be regulated on a local scale during the dynamic developmental processes of dendrite outgrowth, branching, and/or remodeling