New data on the origin of Nesiotites (Soricidae,Mammalia) in Menorca (Balearic Islands,Spain)

The presence of the shrew Nesiotites in Menorca is not yet adequately explained. Some authors consider that its ancestor arrived during the Messinian Salinity Crisis, as happened in Mallorca. Other authors consider that fossil populations in Menorca are the result of a later migration from Mallorca. In this work, several biometrical and morphological characters of abundant fossil populations from both islands have been studied. The results indicate that Early Pleistocene populations in Mallorca and Menorca are rather indistinguishable. Therefore, an early post-Messinian (Pliocene) isolation of Nesiotites in both islands is quite unlikely.     

Une espèce géante de MuscardinusKaup, 1829(Gliridae,Rodentia, Mammalia) dans le gisement karstique de Cala Es Pou (Miocène supérieur de Minorque,Baléares)

In this paper, Muscardinus cyclopeus nov. sp., from the locality of Cala Es Pou, in Menorca (Balearic Islands)), is described. M. cyclopeus is close to M. viretiHugueney & Mein, but shows a greater size. This species belongs to a new phase of insularity in the Balearic Islands, different from the classical Myotragus-Hypnomys-Nesiotites faunas. This phase may be due to variations in the sea level within the Messinian. Other elements belonging to this phase are: Geochelone gymnesicaBate, cf. Alilepus nov. sp. and Rhinolophus cf. grivensis (Deperet).     

A weakened interface in the P182L variant of HSP27 associated with severe Charcot‐Marie‐Tooth neuropathy causes aberrant binding to interacting proteins

HSP27 is a human molecular chaperone that forms large, dynamic oligomers and functions in many aspects of cellular homeostasis. Mutations in HSP27 cause Charcot‐Marie‐Tooth (CMT) disease, the most common inherited disorder of the peripheral nervous system. A particularly severe form of CMT disease is triggered by the P182L mutation in the highly conserved IxI/V motif of the disordered C‐terminal region, which interacts weakly with the structured core domain of HSP27. Here, we observed that the P182L mutation disrupts the chaperone activity and significantly increases the size of HSP27 oligomers formed in vivo, including in motor neurons differentiated from CMT patient‐derived stem cells. Using NMR spectroscopy, we determined that the P182L mutation decreases the affinity of the HSP27 IxI/V motif for its own core domain, leaving this binding site more accessible for other IxI/V‐containing proteins. We identified multiple IxI/V‐bearing proteins that bind with higher affinity to the P182L variant due to the increased availability of the IxI/V‐binding site. Our results provide a mechanistic basis for the impact of the P182L mutation on HSP27 and suggest that the IxI/V motif plays an important, regulatory role in modulating protein–protein interactions.     

Noncytotoxic activation of neutrophils by eosinophil granule major basic protein. Effect on superoxide anion generation and lysosomal enzyme release

Eosinophil granule major basic protein (MBP) and neutrophils have each been implicated in the inflammatory late phase events of allergic disease. Based on this association and flow cytometric evidence presented in this report for MBP binding to neutrophils, we examined the ability of MBP to activate human neutrophils. Incubation of neutrophils with 0.5 to 3.0 microM MBP at room temperature produced a concentration-dependent chemiluminescence (CL) response that peaked after 50 to 70 min. Reduced-and-alkylated MBP, eosinophil cationic protein, and eosinophil-derived neurotoxin did not induce CL. MBP-induced CL was abrogated in the absence of Ca2+ and was absent in neutrophils isolated from two individuals with chronic granulomatous disease. MBP also stimulated release of superoxide anion (O2-) and lysozyme but not beta-glucuronidase or lactate dehydrogenase. Additionally, 1.5 microM MBP in combination with FMLP or platelet-activating factor stimulated a synergistic increase in O2- release from cytochalasin B-treated neutrophils. The degree of synergism with FMLP or platelet-activating factor was inversely related (p less than 0.005) to the level of MBP-induced O2- release. These results indicate that MBP activates neutrophils in a noncytolytic fashion and provide evidence that eosinophil-neutrophil collaboration may contribute to the pathogenesis observed in allergic late phase reactions.     

The amino terminal sequence of sea urchin sperm histone H1 and its phosphorylation by egg cytosol

1. The amino acid sequence of the first 34 residues of sperm histone H1 (SpH1) from Strongylocentrotus purpuratus shows striking similarity with sequences from three South African species. 2. Five contiguous repeats of the tetrapeptide SPBB (where B is R or K) occur between positions 10 and 29. 3. SpH1 was phosphorylated in vitro using egg cytosol as the source of protein kinase and approximately 4.2 mol phosphate were incorporated per mol H1. 4. Sequences of five phosphopeptides of SpH1 show the egg possesses protein kinase activity capable of phosphorylating multiple seryl residues including SPBB in the NH2-, and BBSP in the COOH-end of the protein.     

A-B-O blood groups in Kenya olive baboons (Papio anubis)

A feral population of 183 Kenyan olive baboons representing 5 troops was surveyed for salivary ABO-like antigens. Unlike previously reported populations, a high frequency of the O allele and low frequency of the B allele were detected. This observation may be the result of founder effect and/or genetic drift.