HEAD-SCRATCHING AMONG NORTH AMERICAN WOOD-WARBLERS (PARULIDAE)

A survey of 40 species of 14 genera of North American wood-warblers (Parulidae) reveals that the head-scratching method employed is surprisingly stable within species. The experiments by Nice & Schantz (1959a, b) induced some normally overwing head-scratchers to scratch the head under the wing. It is suggested that this was because their leg rings became caught in secondaries, making normal overwing head-scratching impossible. A few exceptional head-scratching patterns under different conditions invariably involved normally overwing head-scratchers employing the underwing method, and a few species head-scratch under the wing as nestlings but change to overwing before fledging. In all, 31 species appear to be normally overwing head-scratchers, seven are underwing head-scratchers, one species uses both methods and one remains uncertain. There is no evidence for lateral preference in either head-scratching method, and head-scratching is only loosely linked sequentially to preening. The functional significance of head-scratching may be related to blockage of the eustachian tube, or to cleaning and oiling the feathers. Avian head-scratching is more difficult to homologize with mammalian head-scratching than others have considered it to be, but all evidence suggests that within birds underwing head-scratching is phylogenetically primitive. In wood-warblers, the head-scratching method does not correlate with taxonomy. However, ground-dwelling wood-warblers tend to scratch the head under the wing and arboreal wood-warblers over the wing. This correlation provides the first strong clue to the functional significance of the difference between methods in passerine birds.     

Compensatory responses of the fall armyworm (Spodoptera frugiperda) when fed water- and cellulose-diluted diets

Abstract Caterpillars of the noctuid moth, Spodoptera frugiperda (J. E. Smith), reared on artificial diets diluted with cellulose and water, increased fresh weight (fw) consumption 2.2–2.5-fold over those on the undiluted diet. At moderate levels of water- or cellulose-dilution, the increased consumption, combined with increased digestion and absorption of nutrients (ADNU), sufficiently compensated for the reduced nutrient intake to achieve pupal biomass equivalent to that of pupae from the undiluted diet. At higher levels of water- and cellulose-dilution, fw consumption and ADNU increased further but pupal dry weight declined on the water-diluted diets. At each level of dilution fw consumption and ADNU increased similarly on the water- and cellulose-diluted diets, but biomass gain was reduced on the water- compared with the cellulose-diluted diets. This was due in part to lowered food conversion efficiency on the water-diluted diets, possibly caused by increased costs of metabolizing the wetter diets. Our data support the hypothesis that consumption rates are regulated by a nutrient feedback mechanism. Our data also suggest that digestive enzyme activity is correlated with consumption. Furthermore, the cost of increased consumption rates on diets of reduced energetic value may constitute a substantially greater energy expenditure than previously believed. However, this cost was insufficient to reduce relative growth rates but was apparently manifested in lowered lipid accumulation.     

Direct utilization of mannose for mammalian glycoprotein biosynthesis

Direct utilization of mannose for glycoprotein biosynthesis has not been studied because cellular mannose is assumed to be derived entirely from glucose. However, animal sera contain sufficient mannose to force uptake through glucose-tolerant, mannose-specific transporters. Under physiological conditions this transport system provides 75% of the mannose for protein glycosylation in human hepatoma cells despite a 50- to 100-fold higher concentration of glucose. This suggests that direct use of mannose is more important than conversion from glucose. Consistent with this finding the liver is low in phosphomannose isomerase activity (fructose-6-P<->mannose-6-P), the key enzyme for supplying glucose-derived mannose to the N-glycosylation pathway. [2- 3H] Mannose is rapidly absorbed from the intestine of anesthetized rats and cleared from the blood with a t1/2of 30 min. After a 30 min lag, label is incorporated into plasma glycoproteins, and into glycoproteins of all organs during the first hour. Most (87%) of the initial incorporation occurs in the liver, but this decreases as radiolabeled plasma glycoproteins increase. Radiolabel in glycoproteins also increases 2- to 6-fold in other organs between 1-8 h, especially in lung, skeletal muscle, and heart. These organs may take up hepatic- derived radiolabeled plasma glycoproteins. Significantly, the brain, which is not exposed to plasma glycoproteins, shows essentially no increase in radiolabel. These results suggest that mammals use mannose transporters to deliver mannose from blood to the liver and other organs for glycoprotein biosynthesis. Additionally, contrary to expectations, most of the mannose for glycoprotein biosynthesis in cultured hepatoma cells is derived from mannose, not glucose. Extracellular mannose may also make a significant contribution to glycoprotein biosynthesis in the intact organism.      

Tissue-Specific Variation in the Cytokinin Habituation of Cultured Tobacco Cells

Cells of tobacco pith parenchyma sometimes lose their requirement for an exogenous supply of a cell division factor usually supplied as the synthetic cytokinin, kinetin. This change in phenotype, known as cytokinin habituation, is inherited by individual cells and appears to result from epigenetic changes rather than from rare, random, genetic mutations. We have found that tissues from different regions of the tobacco plant exhibit different states of habituation in culture. Pith tissues, as reported earlier, are usually cytokinin requiring and rapidly shift to the habituated state in culture. Leaf tissues are very slightly habituated and require kinetin for optimal rates of growth. Tissues from the stem-cortex are initially habituated. Both the leaf and cortex phenotypes are inherited by individual cells and persist for many cell generations in culture. These results show that certain tissue-specific phenotypes persist in culture and provide evidence that a process akin to habituation leading to different stable states of cytokinin requirement occurs in normal development.     

Initiation of polyene macrolide biosynthesis: interplay between polyketide synthase domains and modules as revealed via domain swapping, mutagenesis, and heterologous complementation

Polyene macrolides are important antibiotics used to treat fungal infections in humans. In this work, acyltransferase (AT) domain swaps, mutagenesis, and cross-complementation with heterologous polyketide synthase domain (PKS) loading modules were performed in order to facilitate production of new analogues of the polyene macrolide nystatin. Replacement of AT(0) in the nystatin PKS loading module NysA with the propionate-specific AT(1) from the nystatin PKS NysB, construction of hybrids between NysA and the loading module of rimocidin PKS RimA, and stepwise exchange of specific amino acids in the AT(0) domain by site-directed mutagenesis were accomplished. However, none of the NysA mutants constructed was able to initiate production of new nystatin analogues. Nevertheless, many NysA mutants and hybrids were functional, providing for different levels of nystatin biosynthesis. An interplay between certain residues in AT(0) and an active site residue in the ketosynthase (KS)-like domain of NysA in initiation of nystatin biosynthesis was revealed. Some hybrids between the NysA and RimA loading modules carrying the NysA AT(0) domain were able to prime rimocidin PKS with both acetate and butyrate units upon complementation of a rimA-deficient mutant of the rimocidin/CE-108 producer Streptomyces diastaticus. Expression of the PimS0 loading module from the pimaricin producer in the same host, however, resulted in production of CE-108 only. Taken together, these data indicate relaxed substrate specificity of NysA AT(0) domain, which is counteracted by a strict specificity of the first extender module KS domain in the nystatin PKS of Streptomyces noursei.     

Colonization of Olive Inflorescences by Verticillium dahliae and its Significance for Pathogen Spread

Verticillium wilt of olive, caused by Verticillium dahliae Kleb., is the most severe disease affecting this crop in most olive growing countries. In this study, the presence of viable structures of V. dahliae in dried inflorescences from wilted olive shoots was investigated. The pathogen was found inside peduncles and flowers, by assessing the number of typical star‐shaped microsclerotial colonies formed onto the modified sodium polypectate agar medium. Microsclerotia of V. dahliae were observed inside the peduncles under the stereoscopic microscope. The presence of microsclerotia in these easily decomposable olive tissues shows that infected inflorescences can act as a source of inoculum for Verticillium wilt epidemics.     

Niche conservatism and species richness patterns of squamate reptiles in eastern and southern Africa

Niche conservatism has been proposed as a mechanism influencing large‐scale patterns of taxonomic richness. We document the species richness patterns of five monophyletic squamate reptile groups (gekkonids, cordylids‐scincids, lacertids, chameleons and alethinophidian snakes) in eastern and southern Africa, and explore if observed patterns reflect niche conservatism processes. We quantified richness and its relationships with current climatic conditions by gridding species' range maps at 110 × 110 km. Also, dated phylogenies and palaeoclimatic reconstructions, coupled with evidence from the fossil record, were used to approximate the areas and climate characteristics in which each group originated and/or radiated. Mean species richness and geographically corrected confidence intervals in current climate types were calculated for each group in order to establish their climatic preferences. On average, the species richness of older groups (gekkonids, cordylids‐scincids and lacertids) was lower in equatorial climates and higher in arid and temperate conditions, whereas more recent groups (chameleons and alethinophidian snakes) were richer in equatorial and temperate climates and less rich in arid conditions. Across all groups, higher richness was associated with climatic characteristics similar to those prevailing at the time in which each group originated/radiated. The congruence of the current climates where reptile groups are richer and the past climates amidst which those groups originated is consistent with an explanation for their diversity gradients based on niche conservatism.     

Selection for EGFR gene amplification in a breast epithelial cell line with basal-like phenotype and hereditary background

An epithelial cell line, referred to as A163, was established from breast carcinoma derived from a patient with a strong family history of breast cancer but no known breast cancer susceptibility mutation. A163 was propagated in a serum-free culture medium including the epidermal growth factor. Immunophenotypic characterization demonstrated a mixed luminal and basal-like phenotype. When epidermal growth factor was excluded from the culture medium, A163 entered a quiescent period followed by a period of increased cell proliferation in a subpopulation of the cells. The epidermal growth factor-independent subpopulation retained the basal-like phenotype of the parental cell line. Karyotype and fluorescent in situ hybridization analysis showed an amplification of epidermal growth factor receptor on 7q in A163-S1 only, resulting in high expression of total and phosphorylated epidermal growth factor receptor. The A163-S1 sub-line piles up in culture, indicating a loss of contact inhibition. When grown on transwell filters, A163 shows basal expression of P63 and cytokeratin 14, whereas A163-S1 expresses P63 ubiquitously, and has lost the basal specific expression of cytokeratin 14, indicating a loss of polarity. Furthermore, when cultured in reconstituted basement membrane matrix, A163 form polarized normal like acini. In contrast, A163-S1 form large disorganized structures with lack of polarity. These cell lines may prove useful to understand molecular changes in breast cancer progression, in particular basal-like breast cancer subtype with bad prognosis and no current treatment options.     

Purification and properties of three esterases from Brevibacterium sp. R312

C. LAMBRECHTS, J. ESCUDERO AND P. GALZY. 1995. The esterases of Brevibacterium sp. R312 were found to have an intracellular location. Electrophoresis of lysed cell supernatant fluids revealed seven bands of esterase activity in the presence of α-naphthyl acetate. Eight esterases were separated by anion exchange chromatography. The three main esterases (esterase 4b, 2 and 4a) of Brevibacterium sp. R312 were purified. The molar masses, the pH optima, the temperature optima and heat stabilities were determined. Esterase 2 differed from the two others in sensitivity to inhibitors. Esterase 4b differed from esterases 2 and 4a in its substrate specificity. This enzyme hydrolyses aliphatic and nitrophenyl esters. The spectrum of activity of the two other esterases is narrower. They hydrolysed only naphthyl esters and, in the case of esterase 2, tributyrate and ethyl butyrate.