Necrophagous or predators? The role of Pheidole radoszkowskii Mayr (Hymenoptera: Formicidae) on Rattus norvegicus (Berkenhout) carcasses (Rodentia: Muridae)

This study aimed to identify the feeding habit of Pheidole radoszkowskii Mayr on Rattus norvegicus (Berkenhout) carcasses, as well as whether its presence limits the occurrence of flies. Pheidole radoszkowskii exhibited more necrophagous than predatory behaviour. Its abundance was inversely proportional to that of flies, confirming that this ant species may cause lesions in carcasses and its presence limits the occurrence of flies. This work clarifies the behaviour of an ant species often encountered on carcasses.     

Chimistes alsaciens à Paris au 19ème siècle: un réseau,une école?

Au 19ème siècle, on remarque la présence, dans la chimie française, d'un nombre considérable d'Alsaciens dont les contributions scientifiques ne peuvent être ignorées. Essentiellement à la suite de la guerre franco-prussienne, leur origine régionale est souvent mise en avant afin de leur attribuer une certaine singularité: mais peut-on distinguer les Alsaciens des autres chimistes français avant 1870? Forment-ils un groupe homogène de par la spécificité de leur lieu d'origine? Cet article a pour but de démontrer que, par leurs options théoriques, leurs relations personnelles et professionnelles et aussi par leur participation à bien d'initiatives communes, ils se sont organisés au sein de la communauté scientifique parisienne. Parmi ces formes d'organisation, on dégage le rôle fondamentale de l'école de recherche du chimiste Adolphe Wurtz (1817–84) qui apu fonctionner comme noyau de ce qu'on peut considérer comme un vrai réseau de chimistes alsaciens à Paris, pendant la seconde moitié du 19ème siècle.     

Functional PCA and Base-Line Logit Models

In many statistical applications data are curves measured as functions of a continuous parameter as time. Despite of their functional nature and due to discrete-time observation, these type of data are usually analyzed with multivariate statistical methods that do not take into account the high correlation between observations of a single curve at nearby time points. Functional data analysis methodologies have been developed to solve these type of problems. In order to predict the class membership (multi-category response variable) associated to an observed curve (functional data), a functional generalized logit model is proposed. Base-line category logit formulations will be considered and their estimation based on basis expansions of the sample curves of the functional predictor and parameters. Functional principal component analysis will be used to get an accurate estimation of the functional parameters and to classify sample curves in the categories of the response variable. The good performance of the proposed methodology will be studied by developing an experimental study with simulated and real data.     

Disruption of CREB function in brain leads to neurodegeneration

Control of cellular survival and proliferation is dependent on extracellular signals and is a prerequisite for ordered tissue development and maintenance. Activation of the cAMP responsive element binding protein (CREB) by phosphorylation has been implicated in the survival of mammalian cells. To define its roles in the mouse central nervous system, we disrupted Creb1 in brain of developing and adult mice using the Cre/loxP system. Mice with a Crem(-/-) background and lacking Creb in the central nervous system during development show extensive apoptosis of postmitotic neurons. By contrast, mice in which both Creb1 and Crem are disrupted in the postnatal forebrain show progressive neurodegeneration in the hippocampus and in the dorsolateral striatum. The striatal phenotype is reminiscent of Huntington disease and is consistent with the postulated role of CREB-mediated signaling in polyglutamine-triggered diseases.     

Transcriptome analysis of the acoelomate human parasite Schistosoma mansoni

Schistosoma mansoni is the primary causative agent of schistosomiasis, which affects 200 million individuals in 74 countries. We generated 163,000 expressed-sequence tags (ESTs) from normalized cDNA libraries from six selected developmental stages of the parasite, resulting in 31,000 assembled sequences and 92% sampling of an estimated 14,000 gene complement. By analyzing automated Gene Ontology assignments, we provide a detailed view of important S. mansoni biological systems, including characterization of metazoa-specific and eukarya-conserved genes. Phylogenetic analysis suggests an early divergence from other metazoa. The data set provides insights into the molecular mechanisms of tissue organization, development, signaling, sexual dimorphism, host interactions and immune evasion and identifies novel proteins to be investigated as vaccine candidates and potential drug targets.     

Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

We identified a deletion of a gene encoding a subunit of RNA polymerases I and III, POLR1D, in an individual with Treacher Collins syndrome (TCS). Subsequently, we detected 20 additional heterozygous mutations of POLR1D in 252 individuals with TCS. Furthermore, we discovered mutations in both alleles of POLR1C in three individuals with TCS. These findings identify two additional genes involved in TCS, confirm the genetic heterogeneity of TCS and support the hypothesis that TCS is a ribosomopathy.     

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

Recently, the application of array-based comparative genomic hybridization (array CGH) has improved rates of detection of chromosomal imbalances in individuals with mental retardation and dysmorphic features. Here, we describe three individuals with learning disability and a heterozygous deletion at chromosome 17q21.3, detected in each case by array CGH. FISH analysis demonstrated that the deletions occurred as de novo events in each individual and were between 500 kb and 650 kb in size. A recently described 900-kb inversion that suppresses recombination between ancestral H1 and H2 haplotypes encompasses the deletion. We show that, in each trio, the parent of origin of the deleted chromosome 17 carries at least one H2 chromosome. This region of 17q21.3 shows complex genomic architecture with well-described low-copy repeats (LCRs). The orientation of LCRs flanking the deleted segment in inversion heterozygotes is likely to facilitate the generation of this microdeletion by means of non-allelic homologous recombination.