Helminths of some tree frogs of the families Hylidae and Phyllomedusidae in an Atlantic rainforest fragment,Brazil

Despite the fact that Brazil is the most-studied country regarding helminths of amphibians, only around 8% of Brazilian anurans have had at least one study made of their helminth fauna. Therefore, the aim of this study was to describe the helminth community of nine species of Atlantic Rainforest anurans of two different families, eight of them with no previous study, and six of which are endemic to Brazil. The analysed hosts for their parasites were: Dendropsophus minutus (n = 48), Scinax auratus (n = 36), D. branneri (n = 33), D. elegans (n = 26), Hypsiboas albomarginatus (n = 22), Pithecopus nordestinus (n = 19), D. decipiens (n = 12), D. haddadi (n = 11) and S. x-signatus (n = 11). A total of 781 helminths were collected from 106 (48.6%) of 218 analysed hosts, 656 Centrorhyncus sp. cystacanths and 125 nematodes: 76 adults (25 Cosmocerca sp.; three Cosmocerceidae gen. sp.; 20 Cosmocerca parva, 20 Cosmocercella phyllomedusae, five Aplectana sp., two Oswaldocruzia sp. and one Rhabdias sp.), 43 encysted larvae (nine Porrocaecum sp. and 34 Brevimulticaecum sp.) and six Physaloptera sp. larvae. Anurans may display many roles within the helminth life cycles, as they act as both predator and prey to a wide variety of animals. Consequently, we have found helminths that use anurans as definitive, intermediate and paratenic hosts. Opposing other surveys in which nematodes are the most prevalent and abundant parasites, acanthocephalans were the most prevalent taxa. These findings highlight the lack of knowledge regarding the helminth fauna of anurans and reveal many gaps with respect to their infection patterns in amphibians.     

More than just scanning: the importance of cap-independent mRNA translation initiation for cellular stress response and cancer

The scanning model for eukaryotic mRNA translation initiation states that the small ribosomal subunit, along with initiation factors, binds at the cap structure at the 5′ end of the mRNA and scans the 5′ untranslated region (5′UTR) until an initiation codon is found. However, under conditions that impair canonical cap-dependent translation, the synthesis of some proteins is kept by alternative mechanisms that are required for cell survival and stress recovery. Alternative modes of translation initiation include cap- and/or scanning-independent mechanisms of ribosomal recruitment. In most cap-independent translation initiation events there is a direct recruitment of the 40S ribosome into a position upstream, or directly at, the initiation codon via a specific internal ribosome entry site (IRES) element in the 5′UTR. Yet, in some cellular mRNAs, a different translation initiation mechanism that is neither cap- nor IRES-dependent seems to occur through a special RNA structure called cap-independent translational enhancer (CITE). Recent evidence uncovered a distinct mechanism through which mRNAs containing N ⁶-methyladenosine (m⁶A) residues in their 5′UTR directly bind eukaryotic initiation factor 3 (eIF3) and the 40S ribosomal subunit in order to initiate translation in the absence of the cap-binding proteins. This review focuses on the important role of cap-independent translation mechanisms in human cells and how these alternative mechanisms can either act individually or cooperate with other cis-acting RNA regulons to orchestrate specific translational responses triggered upon several cellular stress states, and diseases such as cancer. Elucidation of these non-canonical mechanisms reveals the complexity of translational control and points out their potential as prospective novel therapeutic targets.     

The DNA sequence of the human X chromosome

The human X chromosome has a unique biology that was shaped by its evolution as the sex chromosome shared by males and females. We have determined 99.3% of the euchromatic sequence of the X chromosome. Our analysis illustrates the autosomal origin of the mammalian sex chromosomes, the stepwise process that led to the progressive loss of recombination between X and Y, and the extent of subsequent degradation of the Y chromosome. LINE1 repeat elements cover one-third of the X chromosome, with a distribution that is consistent with their proposed role as way stations in the process of X-chromosome inactivation. We found 1,098 genes in the sequence, of which 99 encode proteins expressed in testis and in various tumour types. A disproportionately high number of mendelian diseases are documented for the X chromosome. Of this number, 168 have been explained by mutations in 113 X-linked genes, which in many cases were characterized with the aid of the DNA sequence.     

Real ribozymes suggest a relaxed error threshold

The error threshold for replication, the critical copying fidelity below which the fittest genotype deterministically disappears, limits the length of the genome that can be maintained by selection. Primordial replication must have been error-prone, and so early replicators are thought to have been necessarily short. The error threshold also depends on the fitness landscape. In an RNA world, many neutral and compensatory mutations can raise the threshold, below which the functional phenotype, rather than a particular sequence, is still present. Here we show, on the basis of comparative analysis of two extensively mutagenized ribozymes, that with a copying fidelity of 0.999 per digit per replication the phenotypic error threshold rises well above 7,000 nucleotides, which permits the selective maintenance of a functionally rich riboorganism with a genome of more than 100 different genes, the size of a tRNA. This requires an order of magnitude of improvement in the accuracy of in vitro-generated polymerase ribozymes. Incidentally, this genome size coincides with that estimated for a minimal cell achieved by top-down analysis, omitting the genes dealing with translation.     

Mice deficient in Abl are osteoporotic and have defects in osteoblast maturation

The c-Abl protein is a non-receptor tyrosine kinase involved in many aspects of mammalian development. c-Abl kinase is widely expressed, but high levels are found in hyaline cartilage in the adult, bone tissue in newborn mice, and osteoblasts and associated neovasculature at sites of endochondrial ossification in the fetus. Mice homozygous for mutations in the gene encoding c-Abl (AIM) display increased perinatal mortality, reduced fertility, foreshortened crania and defects in the maturation of B cells in bone marrow. Here we demonstrate that Abl-/- mice are also osteoporotic. The long bones of mutant mice contain thinner cortical bone and reduced trabecular bone volume. The osteoporotic phenotype is not due to accelerated bone turnover--both the number and activity of osteoclasts are similar to those of control littermates--but rather to dysfunctional osteoblasts. In addition, the rate of mineral apposition in the mutant animals is reduced. Osteoblasts from both stromal and calvarial explants showed delayed maturation in vitro as measured by expression of alkaline phosphatase (ALP), induction of mRNA encoding osteocalcin and mineral deposition.     

Myonecrosis induced by scorpion venom

Zusammenfassung Elektronenoptischer Nachweis, dass Skorpiongift (Tityus serrulatus) nach i.p. Verabreichung an der quergestreiften Muskulatur der Küchenschabe eine starke nekrosierende Wirkung ausübt.     

Isolation of Commisterone,a new phytoecdysone fromCyanotis vaga

Zusammenfassung Aus den zerkleinerten Blättern vonCyanotis vaga (Commelinaceae) wurde durch Benzolextraktion und Chromatographie mit Silikagel eine neue Substanz isoliert: C₂₇H₄₄O₇ (Sp. 146–151), die nach den spektrometrischen Daten (IR, NMR, UV, MS) mit dem Insektenhormon Ecdysteron stereoisomer ist.

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Dedicated to Prof. Dr. R. Tschesche, Organisch-Chemisches Institut, Universität Bonn (Germany) on the occasion of his 65th birthday, for the invaluable help and inspiration he has given us.     

Effect of urethan on the glycogen and RNA content of liver parenchymal cells. A cytophotometric study

Résumé Utilisant la méthode cytophotométrique on a observé l'accroissement du glycogène et la réduction de ARN dans le foie de souris soumises au traitement toxique par l'uréthane.     

Potentiation of histamine and inhibition of diamine oxidase by mescaline

Zusammenfassung Anhand zweier Versuchsanordnungen wird gezeigt, dass Meskalin Histaminwirkungen verstärken kann. Ausserdem vermag es die Histamin zerstörende Wirkung der Diaminooxydase zu hemmen (in 10^–5-molarer Konzentration).Es wird die Möglichkeit diskutiert, dass diese Eigenschaften mit der 4-Methoxyphenyl-äthylamin-Struktur des Meskalins in Zusammenhang stehen könnten.