All eukaryotic mRNAs (except organellar) are capped at their 5 end. The cap structure (m 7 GpppN, where N is any nucleotide) is extremely important for the processing and translation of mRNA. Several cap-binding proteins that facilitate these processes have been characterized. Here we describe a novel human cytoplasmic protein that is 30% identical and 60% similar to the human translation initiation factor 4E (eIF4E). We demonstrate that this protein, named 4E Homologous Protein (4EHP), binds specifically to capped RNA in an ATP-and divalent ion-independent manner. The three-dimensional structure of 4EHP, as predicted by homology modeling, closely resembles that of eIF4E and site-directed mutagenesis analysis of 4EHP strongly suggests that it shares with eIF4E a common mechanism for cap binding. A putative function for 4EHP is discussed.

Here we show that the capsid (C) protein of Semliki Forest virus (SFV) contains two nucleolar targeting signals (NOS) responsible for the karyophilic properties of this protein. When conjugated to the non-karyophilic carrier protein bovine serum albumin (BSA), the two synthetic nuclear localization sequences (NLS) of the C protein transferred with equal efficiency the carrier protein into the nucleolus of both higher and lower eukaryotic target cells.

-The worldwide maintenance of the honeybee has major ecological, economic, and political implications. In the present study, electromagnetic waves originating from mobile phones were tested for potential effects on honeybee behavior. Mobile phone handsets were placed in the close vicinity of honeybees. The sound made by the bees was recorded and analyzed. The audiograms and spectrograms revealed that active mobile phone handsets have a dramatic impact on the behavior of the bees, namely by inducing the worker piping signal. In natural conditions, worker piping either announces the swarming process of the bee colony or is a signal of a disturbed bee colony.worker bee / acoustic communication / mobile phone handset / worker piping / induction

Early afferent innervation and differentiation of sensory vestibular cells were studied in mouse embryos from gestation day (GD) 13 to 16. Afferent neurites were found as early as GD 13 in the epithelium when there were no clearly differentiated sensory cells. By GD 14 the earliest sensory cells which exhibited short hair bundles at their luminal pole were then contacted by afferent endings at their basal part. On GD 15 nerve endings establishing specialized synaptic contacts, characterized by asymmetrical membrane densities and synaptic bodies, were observed. At this stage, microtubules contacting the presynaptic membranes, as well as coated vesicles were found. On GD 16 the hair cells were multi-afferented and numerous synaptic bodies were found. These results showing a concomitance between the hair cell differentiation and the establishment of nerve contacts are discussed with particular respect to nerve-hair cell interactions during sensory differentiation. This study does not point to a primary induction of vestibular hair cell differentiation by nerve endings, but it is consistent with the possibility that the ingrowth of nerve fibers is one of many factors that influence the differentiation of receptor cells. With respect to synapse formation, it is assumed that the location of synaptic bodies at presynaptic densities is determined by the arrival of afferent nerve endings.

The development of vestibular receptors in the mouse was studied by scanning electron microscopy between the 13th gestation day to birth. On the 13th gestation day, the utricle was entirely covered with microvilli, which were often grouped around small kinocilia at the center of the macula. The vertical cristae were not clearly differentiated at this stage. On the 15th gestation day, the opposite orientation of ciliary tufts in the utricle indicated the beginnings of the striola. During the whole period studied, gradients in differentiation of ciliary tufts were observed between the center and the periphery of the utricle, and the top and base of the cristae. The auxiliary structures (otolithic membrane and cupula) began to appear at the same time as the first ciliary tufts differentiated. Otoliths, still immature, were only observed as from the 16th gestation day. Differentiation of ciliary tufts on the utricle appeared to be progressive during the fetal period. However, between the 16th and 17th gestation days, a pause in the differentiation of ciliary tufts was registered. A day later, there was a pause in the increase of the utricular sensory surface, which coincided with a temporary stabilization of the decrease in the thickness of the sensory epithelium.

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In the course of postnatal development in the cat, there is a decrease of about 93% in the total number of synaptic bodies (synaptic balls and synaptic bars) in type I hair cells. In type II hair cells, there is no change in the number of synaptic balls. Simultaneously, the length of specialized neuroepithelial contact increases by approximately 300% during type I hair cell maturation. Only the synaptic bars displaying a polylamellar ultrastructure persist in the type I hair cells of the adult animal. It is suggested that the afferent vestibular synapses of the type I hair cell are transformed during ontogeny.

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