Induction of Melanogenesis by Tetradecanoylphorbol‐13 Acetate and Endothelin 3 in Embryonic Avian Peripheral Nerve Cultures

In this study, we have analyzed the melanogenic potential of Schwann cells using in vitro cell cultures of embryonic quail peripheral nerves. It is shown that in Schwann cells, two factors, 12‐O‐tetradecanoylphorbol‐13 acetate (TPA) and endothelin 3, trigger a differentiation pathway toward melanocytes, and that Steel factor has no effect on these cells unless treated simultaneously with TPA. In these cultures, TPA induces the expression of c‐kit, whereas Steel factor enhances the development of melanocytes. In the assay system we employed, neither neuronal nor catecholaminergic phenotypes were obtained, regardless of various combinations of related factors added to the culture medium. These data support our previous observations indicating the existence of bipotent progenitors that are capable of differentiating into Schwann cells or into melanocytes, and the regulatory role of endothelin 3 on those precursors, as revealed by the clonal culture of neural crest cells.     

An assessment of a method based on intrinsic antibiotic resistance for identifying Rhizobium strains

A method based on intrinsic antibiotic resistance (IAR) for identifying large numbers of Rhizobium strains was assessed and found to be unsatisfactory for R. phaseoli and isolates from Cicer arietinum (Rhizobium spp.). Our data showed that the number of different IAR patterns always exceeded the number of strains tested. With 90 nodule isolates from plants inoculated with a mixture of three strains of R. Phaseoli, the technique gave 18 different resistance patterns. When 24 strains of Rhizobium spp., each replicated three times, were examined 68 different resistance patterns were obtained. Single colony isolates from one strain also gave several different IAR patterns. All strains tested with fluorescent“ antibody were readily identified. Attempts to obtain correct strain identification with IAR by simplifying the scoring systems or allowing up to two differences in the resistance patterns were unsuccessful. We were unable to define the source of this variation although incubation time and inoculum concentration were shown to affect the IAR patterns     

Delayed setting of the photoperiodic response in recombinant clones of the aphid species Sitobion avenae

1. To explore the possible causes of apparent changes in reproductive mode from obligate to cyclical parthenogenesis over time in recombinant clones of the aphid Sitobion avenae Fabricius, all F1 progenies from various crosses were tested for several consecutive years for sexual morph production, after several weeks' exposure to a short photoperiod. 2. Variable proportions of the F1 progenies from selfing and outcrossing holocyclic clones did not produce mating females when induction was attempted in the year of hatching, but only after further induction, the following year or after. This ‘delayed setting of the photoperiodic response’ (DSPR) was much stronger in recombinants from crosses involving only clones from oceanic regions than in those involving one clone from a region with a continental climate. 3. F1 progenies resulting from crosses between one holocyclic and one intermediate clone did not show DSPR. It appeared again in the F2. 4. DSPR preferentially affected the latest hatched clones in a given progeny. 5. This phenomenon is neither an experimental artefact nor as a result of clone contamination. It appears to be because of a genetically controlled quantitative trait affecting the length of the ‘interval timer’, and may represent an adaptation of holocyclic aphid clones from oceanic regions to unpredictable winter climates.