TL;DR: The results, which confirm and extend earlier observations, suggest that (TTAGG)n was a phylogenetically ancestral telomere motif in the insect lineage but was lost independently in different groups, being replaced probably by other telomeres motifs.
Abstract: We studied the occurrence of the TTAGG telomere repeats by fluorescence in-situ hybridization (FISH) and Southern hybridization in ten insect species and two other arthropods. (TTAGG)n-containing telomeres were found in three Lepidoptera species, the silkworm Bombyx mori (in which the telomeric sequence was recently discovered), the flour moth Ephestia kuehniella, and the wax moth Galleria mellonella, in one species of Hymenoptera, the honey bee Apis mellifera, in one species of Coleoptera, the bark beetle Ips typographus, in one species of Orthoptera, the locust Locusta migratoria, and in a crustacean, the amphipod Gammarus pulex. They were absent in another species of Coleoptera, the mealworm Tenebrio molitor, two representatives of Diptera, Drosophila melanogaster and Megaselia scalaris, a species of Heteroptera, the bug Pyrrhocoris apterus and a spider, Tegenaria ferruginea. Our results, which confirm and extend earlier observations, suggest that (TTAGG)n was a phylogenetically ancestral telomere motif in the insect lineage but was lost independently in different groups, being replaced probably by other telomere motifs. In the Coleoptera this must have happened rather recently as even members of the same family, Curculionidae, differ with respect to the telomeric DNA.
TL;DR: The first report on inducible antibacterial molecules in the sap-sucking bug Pyrrhocoris apterus, a representative species of the Hemiptera, which predated the Endoptergotes by at least 50 million years in evolution is presented.
Abstract: Insects belonging to the recent orders of the endopterygote clade (Lepidoptera, Diptera, Hymenoptera and Coleoptera) respond to bacterial challenge by the rapid and transient synthesis of a battery of potent antibacterial peptides which are secreted into their haemolymph. Here we present the first report on inducible antibacterial molecules in the sap-sucking bug Pyrrhocoris apterus, a representative species of the Hemiptera, which predated the Endoptergotes by at least 50 million years in evolution. We have isolated and characterized from immune blood of this species three novel peptides or polypeptides: (i) a 43-residue cysteine-rich anti-(Gram-positive bacteria) peptide which is a new member of the family of insect defensins; (ii) a 20-residue proline-rich peptide carrying an O-glycosylated substitution (N-acetylgalactosamine), active against Gram-negative bacteria; (iii) a 133-residue glycine-rich polypeptide also active against Gram-negative bacteria. The proline-rich peptide shows high sequence similarities with drosocin, an O-glycosylated antibacterial peptide from Drosophila, and also with the N-terminal domain of diptericin, an inducible 9 kDa antibacterial peptide from members of the order Diptera, whereas the glycine-rich peptide has similarities with the glycine-rich domain of diptericin. We discuss the evolutionary aspects of these findings.
TL;DR: A sesquiterpenoid ester with high juvenile hormone activity for Pyrrhocoris apterus was isolated from balsam fir, Abies balsamea (L.) Miller, and identified as the methyl ester of todomatuic acid.
Abstract: A sesquiterpenoid ester with high juvenile hormone activity for Pyrrhocoris apterus (L.) was isolated from balsam fir, Abies balsamea (L.) Miller, and identified as the methyl ester of todomatuic acid.
TL;DR: The results suggest that accumulation of PaHsp70 belongs to a complex cold tolerance adaptation in the insect Pyrrhocoris apterus.
Abstract: Background
The Pyrrhocoris apterus (Insecta: Heteroptera) adults attain high levels of cold tolerance during their overwintering diapause. Non-diapause reproducing adults, however, lack the capacity to express a whole array of cold-tolerance adaptations and show relatively low survival when exposed to sub-zero temperatures. We assessed the competence of non-diapause males of P. apterus for responding to heat- and cold-stresses by up-regulation of 70 kDa heat shock proteins (Hsps) and the role of Hsps during repair of heat- and cold-induced injury.
Principal Findings
The fragments of P. apterus homologues of Hsp70 inducible (PaHsp70) and cognate forms (PaHsc70) were cloned and sequenced. The abundance of mRNA transcripts for the inducible form (qPCR) and corresponding protein (Western blotting) were significantly up-regulated in response to high and low temperature stimuli. In the cognate form, mRNA was slightly up-regulated in response to both stressors but very low or no up-regulation of protein was apparent after heat- or cold-stress, respectively. Injection of 695 bp-long Pahsp70 dsRNA (RNAi) caused drastic suppression of the heat- and cold-stress-induced Pahsp70 mRNA response and the up-regulation of corresponding protein was practically eliminated. Our RNAi predictably prevented recovery from heat shock and, in addition, negatively influenced repair of chilling injuries caused by cold stress. Cold tolerance increased when the insects were first exposed to a mild heat shock, in order to trigger the up-regulation of PaHsp70, and subsequently exposed to cold stress.
Conclusion
Our results suggest that accumulation of PaHsp70 belongs to a complex cold tolerance adaptation in the insect Pyrrhocoris apterus.
TL;DR: A description of Stevens' "Voice level: autophonic scale, perceived loudness, and effects of sidetone," in Handbook of Mathematical Psychology, vol.
Abstract: 60-67 (1960); Stevens, J. C., and S. S. Stevens, \"Warmth and cold: dynamics of sensory intensity,\" J. Exptl. Psychol., 60, 183-192 (1960); Stevens, S. S., and J. R. Harris, \"The scaling of subjective roughness and smoothness,\" J. Exptl. Psychol., 64, 489-494 (1962); Stevens, S. S., and M. Guirao, \"Subjective scaling of length and area and the matching of length to loudness and brightness,\" J. Exptl. Psychol., 66, 177-186 (1963). 2 Luce, R. D., and E. Galanter, \"Psychophysical scaling,\" in Handbook of Mathematical Psychology, ed. R. D. Luce, R. R. Bush, and E. Galanter (New York: John Wiley and Sons, 1963), vol. 1, pp. 245-307. 3 For a description see Stevens, J. C., and M. Guirao, \"Individual loudness functions,\" J. Acoust. Soc. Am., 36, 2210-2213 (1964). 4Stevens, S. S., \"Calculation of the loudness of a complex noise,\" J. Acoust. Soc. Am., 28, 807832 (1956); Stevens, S. S., \"Problems and methods of psychophysics,\" Psychol. Bull., 55, 177-196 (1958). 6 Stevens, S. S., \"On the brightness of lights and the loudness of sounds,\" Science (Abstracts), 118, 576 (1953); Onley, J. W., 'Light adaptation and the brightness of brief foveal stimuli,\" J. Opt. Soc. Am., 51, 667-673 (1961); Stevens, J. C., and S. S. Stevens, \"Brightness function: effects of adaptation,\" J. Opt. Soc. Am., 53, 375-385 (1963). 6 Stevens, S. S., \"Procedure for calculating loudness, Mark VI,\" J. Acoust. Soc. Am., 33, 15771585 (1961); Harper, R., and S. S. Stevens, \"Subjective hardness of compliant materials,\" Quart. J. Exptl. Psychol., 16, 204-215 (1964). 7 Lane, H. L., A. C. Catania, and S. S. Stevens, \"Voice level: autophonic scale, perceived loudness, and effects of sidetone,\" J. Acoust. Soc. Am., 33, 160-167 (1961). 8 Stevens, J. C., and S. S. Stevens, \"Brightness function: effects of adaptation,\" J. Opt. Soc. Am., 53, 375-385 (1963).