Microheterogeneity of human galactose-1-Phosphate uridylyl transferase. Isoelectrofocusing results

Using thin-layer acrylamide gel isoelectrofocusing, several bands of galactose-1-Phosphate uridylyl transferase were found in various human tissues. Liver transferase, as well as that of some other tissues, was resolved into several bands with pHi between 5.30 and 5.80; red cell enzyme was resolved into five bands with pHi between 5.0 and 5.45. The comparison of erythrocytes with their precursors, reticulocytes and erythroblasts, showed a striking difference: the pHi of the erythroblast enzyme was between 5.55 and 5.90 and that of reticulocytes between 5.30 and 5.50. It is possible that molecular aging is the cause of the anodisation of the erythrocyte transferase and the microheterogeneity of the enzyme observed in other tissues.     

Conspicuous endolithic algal associations in a mesophotic reef-building coral

Coral Reefs - Understanding how corals and their symbionts specialize across depth gradients allows us to understand biodiversity in shallow and mesophotic coral ecosystems. Here we determined the...     

Genome‐wide evidence for divergent selection between populations of a major agricultural pathogen

The genetic and environmental homogeneity in agricultural ecosystems is thought to impose strong and uniform selection pressures. However, the impact of this selection on plant pathogen genomes remains largely unknown. We aimed to identify the proportion of the genome and the specific gene functions under positive selection in populations of the fungal wheat pathogen Zymoseptoria tritici. First, we performed genome scans in four field populations that were sampled from different continents and on distinct wheat cultivars to test which genomic regions are under recent selection. Based on extended haplotype homozygosity and composite likelihood ratio tests, we identified 384 and 81 selective sweeps affecting 4% and 0.5% of the 35 Mb core genome, respectively. We found differences both in the number and the position of selective sweeps across the genome between populations. Using a XtX‐based outlier detection approach, we identified 51 extremely divergent genomic regions between the allopatric populations, suggesting that divergent selection led to locally adapted pathogen populations. We performed an outlier detection analysis between two sympatric populations infecting two different wheat cultivars to identify evidence for host‐driven selection. Selective sweep regions harboured genes that are likely to play a role in successfully establishing host infections. We also identified secondary metabolite gene clusters and an enrichment in genes encoding transporter and protein localization functions. The latter gene functions mediate responses to environmental stress, including interactions with the host. The distinct gene functions under selection indicate that both local host genotypes and abiotic factors contributed to local adaptation.     

Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific Manner

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Modified merozoite surface protein-1 peptides with short alpha helical regions are associated with inducing protection against malaria.

The merozoite surface protein-1 represents a prime candidate for development of a malaria vaccine. Merozoite surface protein-1 has been shown to demonstrate high-activity peptide binding to human red blood cells. One of the high-activity binding peptides, named 5501, located in the N-terminus (amino acid sequence MLNISQHQCVKKQCPQNS) of the 19-kDa molecular mass fragment of merozoite surface protein-1, is conserved, nonimmunogenic and nonprotective. Its critical binding residues were identified and replaced with amino acids of similar mass but different charge, in order to modify their immunogenic and protective characteristics. Three analogues with positive or negative immunological results were studied by nuclear magnetic resonance to correlate their three-dimensional structure with their biological functions. The studied peptides presented alpha-helical fragments, but in different peptide regions and extensions, except for randomly structured 5501. We show that altering a few amino acids induced immunogenicity and protectivity against experimental malaria and changed the peptide three-dimensional structure, suggesting a better fit with immune-system molecules.     

L'ultrastructure de l'adénohypophyse du crapaud Bufo bufo L.

Résumé Cinq types de cellules granulées se différencient au cours de la métamorphose dans la pars distalis de l'hypophyse du têtard de Crapaud.A la prémétamorphose apparaissent les deux types de cellules protidiques, les cellules glycoprotidiques de type II et des cellules glycoprotidiques d'un type intermédiaire. Cette dernière catégorie cellulaire disparaît au climax.A la prométamorphose se différencient les cellules glycoprotidiques de type IV.Au climax s'observent les cellules glycoprotidiques de type III.Les cellules glycoprotidiques de type II sont vraisemblablement responsables de la sécrétion de l'hormone thyréotrope (TSH). Il n'est pas encore possible de préciser la fonction des autres types cellulaires.Des fibres nerveuses ont pu être observées dans la pars distalis entre les cellules granulées.

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The ultrastructure of the adenohypophysis in the toad, Bufo bufo L.III. Cell differentiation in the pars distalis during larval growth

Summary Five granulated cell types can be distinguished in the Toad's pars distalis during larval growth.During premetamorphosis the two types of protidic cells appear, the glycoprotein containing cells of type II and an intermediary cell type which disappears during the climax.During prometamorphosis the glycoprotein cells of type IV are apparent.During the climax the glycoprotein cells of type III can be observed.The glycoprotein containing cells of type II probably produce the thyroid-stimulating-hormone (TSH). The function of the other cell types can not be specified for the moment.Nervous fibers have been observed in the pars distalis between granulated cells.

Tous nos remerciements vont à Mme Sidler-Ansermet photographe, Mlle Schorderet secrétaire, et Mlle Schutz technicienne, de l'aide qu'elles ont apportée à la réalisation de ce mémoire.     

Rational design of a monomeric and photostable far‐red fluorescent protein for fluorescence imaging in vivo

Fluorescent proteins (FPs) are powerful tools for cell and molecular biology. Here based on structural analysis, a blue‐shifted mutant of a recently engineered monomeric infrared fluorescent protein (mIFP) has been rationally designed. This variant, named iBlueberry, bears a single mutation that shifts both excitation and emission spectra by approximately 40 nm. Furthermore, iBlueberry is four times more photostable than mIFP, rendering it more advantageous for imaging protein dynamics. By tagging iBlueberry to centrin, it has been demonstrated that the fusion protein labels the centrosome in the developing zebrafish embryo. Together with GFP‐labeled nucleus and tdTomato‐labeled plasma membrane, time‐lapse imaging to visualize the dynamics of centrosomes in radial glia neural progenitors in the intact zebrafish brain has been demonstrated. It is further shown that iBlueberry can be used together with mIFP in two‐color protein labeling in living cells and in two‐color tumor labeling in mice.