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Social environments are notoriously multifactorial, yet studies in rodents have suggested that single variables such as maternal care can in fact be disentangled and correlated with specific DNA methylation changes. This study assesses whether non-detrimental social environmental variation in a highly plastic social insect is correlated with epigenomic modifications at the DNA methylation level. Honey bee workers perform tasks such as nursing and foraging in response to the social environment in the hive, in an age-linked but not age-dependent manner. In this study, the methylation levels of 83 cytosine-phosphate-guanosine dinucleotides over eight genomic regions were compared between the brains of age-matched bees performing nursing or foraging tasks. The results reveal more changes correlated with task than with chronological age, and also hive-associated methylation at some sites. One methylation site from a gene encoding Protein Kinase C binding protein 1 was consistently more methylated in foragers than nurses, which is suggested to lead to production of task-specific protein isoforms via alternative splicing. This study illustrates the ability of the neural epigenome to dynamically respond to complex social stimuli. [ABSTRACT FROM AUTHOR]

A defining characteristic of eusocial animals is their division of labour into reproductive and nonreproductive specialists. Here, we used a microarray study to identify genes associated with functional sterility in the worker honey bee Apis mellifera. We contrasted gene expression in workers from a functionally sterile wild-type strain with that in a mutant (anarchist) strain selected for high rates of ovary activation. We identified a small set of genes from the brain ( n = 7) and from the abdomen ( n = 5) that are correlated in their expression with early stages of ovary activation. Sterile wild-type workers up-regulated two unknown genes and a homologue of Drosophila CG6004. By contrast, reproductive anarchist workers up-regulated genes for the yolk protein vitellogenin, venom peptides and a member of the AdoHycase superfamily, among others. The differentially expressed genes identified are likely to be involved in early differentiation into sterile and reproductive worker phenotypes and may therefore form part of the gene networks associated with the regulation of honey bee worker sterility. Our study may have lacked sufficient power to detect all but a minority of biologically relevant changes taking place; however, the differential expression of vitellogenin and a putative AdoHycase suggests that our screen has captured core reproductive genes and that ovary activation may involve an epigenetic mechanism. [ABSTRACT FROM AUTHOR]

We show that differences in the reproductive development of honey bee workers are associated with locus-specific changes to abundance of messenger RNA. Using a cross-fostering field experiment to control for differences related to age and environment, we compared the gene expression profiles of functionally sterile workers (wild-type) and those from a mutant strain in which workers are reproductively active (anarchist). Among the set of three genes that are significantly differentially expressed are two major royal jelly proteins that are up-regulated in wild-type heads. This discovery is consistent with sterile workers synthesizing royal jelly as food for developing brood. Likewise, the relative underexpression of these two royal jellies in anarchist workers is consistent with these workers’ characteristic avoidance of alloparental behaviour, in favour of selfish egg-laying. Overall, there is a trend for the most differentially expressed genes to be up-regulated in wild-type workers. This pattern suggests that functional sterility in honey bee workers may generally involve the expression of a suite of genes that effectively ‘switch’ ovaries off, and that selfish reproduction in honey bee workers, though rare, is the default developmental pathway that results when ovary activation is not suppressed. [ABSTRACT FROM AUTHOR]

In this work we present structural, optical and electrical properties of GaN epilayers and AlGaN/GaN MOCVD heterostructures obtained on polar and non-polar 10x10 mm2, 1 and 1.5 inch bulk ammonothermal GaN substrates. The results were obtained based not only on a single-point measurement but also on mapping across the sample area. In contactless electroreflectance (CER) spectra CER resonances related to optical transitions between excited states were clearly observed for GaN/AlGaN QWs grown on c -plane GaN substrates, whereas such features were not noted in the case of GaN/AlGaN QWs grown on m -plane GaN substrates. This experimental result clearly shows that the polarization-related electric field leads to the quantum confinement of some extra states in the polar QW system. To check the advantage of homo-epitaxy using ammonothermal GaN, high electron mobility transistors (HEMTs), and light emitting diodes (LEDs) structures were grown on (0001) Ga-polarity, semi-insulating and conductive GaN substrates respectively (© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [ABSTRACT FROM AUTHOR]

Carbohydrate-metabolizing enzymes may have particularly interesting roles in the honey bee, Apis mellifera, because this social insect has an extremely carbohydrate-rich diet, and nutrition plays important roles in caste determination and socially mediated behavioural plasticity. We annotated a total of 174 genes encoding carbohydrate-metabolizing enzymes and 28 genes encoding lipid-metabolizing enzymes, based on orthology to their counterparts in the fly, Drosophila melanogaster, and the mosquito, Anopheles gambiae. We found that the number of genes for carbohydrate metabolism appears to be more evolutionarily labile than for lipid metabolism. In particular, we identified striking changes in gene number or genomic organization for genes encoding glycolytic enzymes, cellulase, glucose oxidase and glucose dehydrogenases, glucose-methanol-choline (GMC) oxidoreductases, fucosyltransferases, and lysozymes. [ABSTRACT FROM AUTHOR]

Transparency of truly bulk GaN substrates obtained by ammonothermal method was measured in the mid infrared spectral range by Fourier spectroscopy. The same measurements were performed for GaN templates grown by meatlorganic vapour phase epitaxy on sapphire and SiC substrates. It has been clearly observed that truly bulk GaN substrates are transparent up to ∼7 µm whereas GaN templates grown on sapphire and SiC are transparent only up to ∼6.5 and ∼5.5 µm, respectively, due to non-transparency of sapphire and SiC in this spectral range. It has been shown that the transparency 'cut off' at ∼7 µm for GaN crystals results from the absorption of light by the second harmonic of optical phonons, which is very significant due to the strong electron-phonon coupling in this material. Also it has been clearly presented that the absorption 'cut-off' in the infrared spectral region can be easily tuned by increasing of free carrier concentration in GaN. It was observed that the infrared transparency can be shifted from ∼7 to ∼2 µm or even shorter wavelengths when the electron concentration is increased up to ∼1019 cm-3. (© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [ABSTRACT FROM AUTHOR]