Fras1 deficiency results in cryptophthalmos,renal agenesis and blebbed phenotype in mice

Loss of tight association between epidermis and dermis underlies several blistering disorders and is frequently caused by impaired function of extracellular matrix (ECM) proteins. Here we describe a new protein in mouse, Fras1, that is specifically detected in a linear fashion underlying the epidermis and the basal surface of other epithelia in embryos. Loss of Fras1 function results in the formation of subepidermal hemorrhagic blisters as well as unilateral or bilateral renal agenesis during mouse embryogenesis. Postnatally, homozygous Fras1 mutants have fusion of the eyelids and digits and unilateral renal agenesis or dysplasia. The defects observed in Fras1-/- mice phenocopy those of the existing bl (blebbed) mouse mutants, which have been considered a model for the human genetic disorder Fraser syndrome. We show that bl/bl homozygous embryos are devoid of Fras1 protein, consistent with the finding that Fras1 is mutated in these mice. In sum, our data suggest that perturbations in the composition of the extracellular space underlying epithelia could account for the onset of the blebbed phenotype in mouse and Fraser syndrome manifestation in human.     

Towards uranium catalysts

The forefront of research into the complexes of uranium reveals chemical transformations that challenge and expand our view of this unique element. Certain ligands form multiple bonds to uranium, and small, inert molecules such as nitrogen and carbon dioxide become reactive when in complex with the metal. Such complexes provide clues to the catalytic future of uranium, in which the applications of the element extend far beyond the nuclear industry. Most excitingly, the ability of uranium to use its outermost f electrons for binding ligands might enable the element to catalyse reactions that are impossible with conventional, transition-metal catalysts.     

Contribution à l'étude de l'acide chondroïtine-sulfurique

Summary It is found that chondroitinsulfuric acid is composed of unbranched chain-molecules containing rests of glucuronic acid and N-acetyl-galactosamine-6-sulfate combined in one of the following manners (a) or (b):      

Does Paramecium primaurelia use a different genetic code in its macronucleus?

It has long been known that messenger RNAs (mRNAs) of ciliates and in particular of Paramecium are not translated well in heterologous in vitro translation systems. Recently, we have demonstrated for Paramecium primaurelia that this phenomenon results from the presence of well-defined blocking sites in the coding sequences of almost all mRNAs, and that these sites are an intrinsic feature of the primary as opposed to the secondary structure of the mRNAs. Here we show that both the gene and the mRNA for the G surface antigen of P. primaurelia contain numerous TAA and TAG codons scattered throughout their coding sequences. We propose that these codons do not represent termination codons in P. primaurelia but instead code for glutamic acid or glutamine and that the in vitro translation of Paramecium mRNAs is blocked by their presence.     

Minibiotus acadianus (Eutardigrada: Macrobiotidae), a new species of Tardigrada from southern Louisiana, U.S.A.

Over 200 species of freshwater and terrestrial water bears (phylum Tardigrada) are known to occur in North America. Of these, 16 species have been collected in Louisiana. Foliose and fruticose lichens collected on 18 April 2010 in Acadia Parish, Louisiana, were stored in paper envelopes and later soaked in tap water overnight. Tardigrade specimens and eggs were extracted and mounted in polyvinyl lactophenol. The samples contained a new species of tardigrade. Minibiotus acadianus sp. n. has a buccal tube with single anterior curvature, 2 macroplacoids and 1 microplacoid. Small gibbosities are present on the fourth pair of legs, in 3 caudal rows, and in a single row at the level of the third pair of legs. Minibiotus acadianus sp. n. differs from the most similar tardigrade species, Minibiotus fallax (found in Australia and Florida), in having a shorter and wider buccal tube, a different pattern of gibbosities, and short, peg-shaped processes in addition to long, filamentous processes on the eggs. Reexamination of specimens identified as M. fallax in an earlier paper on the Tardigrada of Louisiana indicates that they are, in fact, M. acadianus sp. n., suggesting that the new species is widely distributed in Louisiana. Se conocen más de 200 especies de osos de agua (phylum Tardigrada) terrestres y de agua dulce que ocurren en Norteamérica. De éstas, 16 se han colectado en Louisiana. Se colectaron líquenes foliosos y fruticosos en la parroquia de Acadia, Louisiana, el 18 de abril de 2010, los cuales fueron guardados en sobres de papel y después remojados en agua de la llave durante toda la noche. Se extrajeron especímenes y huevos de tardígrados y se fijaron en polivinilo lactofenol. Las muestras contenían una nueva especie de tardígrado. Minibiotus acadianus sp. n. tiene un tubo bucal con una única curvatura anterior, dos macroplacoides y un microplacoide. Pequeñas gibosidades están presentes en el cuarto par de patas, en tres hileras caudales y en una sola hilera al nivel del tercer par de patas. Minibiotus acadianus sp. n. difiere de la especie más próxima, Minibiotus fallax, una especie que se encontró en Australia y Florida, porque tiene un tubo bucal más corto y ancho, un patrón distinto de gibosidades y apófisis cortas en forma de estaquilla en los huevos, además de apófisis largas y filamentosas. Una reexaminación de los especímenes identificados como M. fallax en una publicación previa sobre los tardígrados de Louisiana indica que son más bien M. acadianus sp. n., lo cual sugiere que esta nueva especie tiene una distribución extensa en Louisiana.     

Analysis of <Emphasis Type="Italic">Dictyostelium</Emphasis> TACC reveals differential interactions with CP224 and unusual dynamics of <Emphasis Type="Italic">Dictyostelium</Emphasis> microtubules

We have localized TACC to the microtubule-nucleating centrosomal corona and to microtubule plus ends. Using RNAi we proved that Dictyostelium TACC promotes microtubule growth during interphase and mitosis. For the first time we show in vivo that both TACC and XMAP215 family proteins can be differentially localized to microtubule plus ends during interphase and mitosis and that TACC is mainly required for recruitment of an XMAP215-family protein to interphase microtubule plus ends but not for recruitment to centrosomes and kinetochores. Moreover, we have now a marker to study dynamics and behavior of microtubule plus ends in living Dictyostelium cells. In a combination of live cell imaging of microtubule plus ends and fluorescence recovery after photobleaching (FRAP) experiments of GFP-α-tubulin cells we show that Dictyostelium microtubules are dynamic only in the cell periphery, while they remain stable at the centrosome, which also appears to harbor a dynamic pool of tubulin dimers.     

Some observations on the Rohon-Beard cell perikaryon.

During the hatching period, the Rohon-Beard cells of Salmo gairdneri showed definite structural maturity of their perikarya, which is in contrast to the amphibian species investigated, where neuronal maturation of the Rohon-Beard cells is finished only in later -- posthatching -- developmental stages.