Smiling Gurken gradient: An expansion of the Gurken gradient

Morphogen gradients provide unique positional information within a tissue. Cells that are sensitive to the concentration of the morphogen integrate this signal and develop an appropriately distinct cell fate. A morphogen gradient is usually generated by a restricted source and shaped by the speed of diffusion and stability of the signaling molecule. In addition, the availability of receptor and Heparan Sulfate Proteoglycans (HSPGs) help to shape the gradient. We have shown that overexpression of Dally-like protein (Dlp) causes an expansion of Gurken distribution and a loss of cell fates which are specified by high levels of epidermal growth factor receptor (Egfr) signaling. In this article, we discuss how D-Cbl mediated Egfr endocytosis and the levels of Dlp affect the shape of the Gurken gradient.     

A low-cost gradient programmer

Equations are given for minimizing the cost and calculating the maximum practical rates for coupled assays when two or more coupling enzymes are involved, and a lag of a predetermined size can be tolerated. The lag caused by obligatory mutarotation of an intermediate is also calculated.     

A field test of the stress‐gradient hypothesis along an aridity gradient

Aims: The stress‐gradient hypothesis (SGH) predicts how plant interactions change along environmental stress gradients. We tested the SGH in an aridity gradient, where support for the hypothesis and the specific shape of its response curve is controversial. Location: Almería, Cáceres and Coimbra, three sites in the Iberian Peninsula that encompass the most arid and wet habitats in the distribution range of a nurse shrub species –Retama sphaerocarpa L. (Boiss) – in Europe. Methods: We analysed the effect of Retama on its understorey plant community and measured the biomass and species richness beneath Retama and in gaps. We estimated the frequency (changes in species richness), importance and intensity of the Retama effects, and derived the severity–interaction relationship pattern, analysing how these interaction indices changed along this aridity gradient. Results and conclusions: The intensity and frequency of facilitation by Retama increased monotonically with increasing environmental severity, and the importance tended to have a similar pattern, overall supporting the SGH. Our data did not support predictions from recent revisions of the SGH, which may not apply to whole plant communities like those studied here or when interactions are highly asymmetrical. Facilitation by Retama influenced community composition and species richness to the point that a significant fraction of species found at the most arid end of the gradient were only able to survive beneath the nurse shrub, whereas some of these species were able to thrive in gaps at more mesic sites, highlighting the ecological relevance of facilitation by nurse species in mediterranean environments, especially in the driest sites.     

Improving the refolding of NTA protein by urea gradient and arginine gradient size-exclusion chromatography

Inclusion body refolding processes play a major role in the production of recombinant proteins. Improvement of the size-exclusion chromatography refolding process was achieved by combining a decreasing urea gradient with an increasing arginine gradient (two gradients) for the refolding of NTA protein (a new thrombolytic agent) in this paper. Different refolding methods and different operating conditions in two gradients gel filtration process were investigated with regard to increasing the NTA protein activity recovery and inhibition of aggregation. The refolding of denatured NTA protein showed this method could significantly increase the activity recovery of protein at high protein concentration. The activity recovery of 37% was obtained from the initial NTA protein concentration up to 20 mg/ml. The conclusions presented in this study could also be applied to the refolding of lysozyme.     

Ion gradient and photoreceptor sensitivity

Summary In superposition eyes of moths (Deilephila elpenor, Manduca sexta) and a neuropteran (Ascalaphus macaronius) receptor excitation and adaptation depend on the limited store of available ion charges in the extra-cellular space.Na⁺ is the main charge carrier necessary for excitation. Receptor mass responses (measured by extracellular electrodes) can, however, be elicited also after complete removal of Na⁺ from the extra-ommatidial space. Responses are also obtained when Na⁺ is partially replaced by Ca⁺⁺ or Mg⁺⁺. These results suggest that the extra-ommatidial space is separated from the intra-ommatidial (rhabdomeric) extra-cellular space. Ion flow between these spaces is slow. The ion exchange during illumination probably takes place over the rhabdomeric part of the photoreceptor membrane.The Na⁺ concentration in the rhabdomeric extracellular space is about 150 mM, as shown by flame photometry. This result supports the assumption that this space is the common Na⁺ store for the three receptor types (UV, green, violet).Positive (optic lobe positive) DC polarization of the retina causes a reduction in the amplitude of the mass responses to light. After cessation of the polarization the amplitude increases with a time constant similar to that after strong illumination. Negative polarization accelerates the rate of increase in amplitude during dark adaptation, while positive polarization retards the increase. These results suggest that one important factor determining the time course of sensitivity increase during dark adaptation is the reestablishment of the Na⁺ gradient over the rhabdomeric membrane.There is a strong electric coupling between the three receptor types in the ommatidium, since all receptors share the same limited intra-ommatidial extra-cellular ion store. Strong illumination of one receptor reduces the ion gradient (extra- to intracellular) also for the other receptors (not absorbing the light). Thereby the sensitivity of the non-illuminated receptors is also reduced. The electric coupling probably improves the wavelength discrimination by the receptors, by keeping almost constant the relative sensitivity of all three receptor types during shortlasting strong selective adaptation of one or two receptor types.The time course of the resistance change over the receptor membrane (measured extra-cellularly) during and after illumination, suggests that during illumination the Na⁺ influx is reduced, and that the ion gradient over the receptor membrane is at least partially re-established already during the illumination.We are grateful to Dr. A.H. Baumhover (United States Department of Agriculture, Agricultural Research Service, Oxford, North Carolina 27565, USA) for supplying theManduca pupae. The work was supported by the Deutsche Forschungsgemeinschaft, SFB 114 and Rezeptorphysiologie; and by Karolinska Institutets Fonder.