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“Blindness induces processes of neural plasticity, resulting in recruitment of the deafferentated visual areas for non-visual sensory functions. These processes are related to superior abilities of blind compared with sighted individuals for specific auditory and tactile tasks. Recently, an ABT-199 order exceptional performance of the blind has been demonstrated for auditory motion perception, with

a minimum audible movement angle that was half that of sighted controls (J. Lewald (2013) Neuropsychologia, 51, 181–186). The present study revealed an electrophysiological correlate of this finding by analysing the so-called motion-onset response, a prominent auditory-evoked potential to the onset of motion. The cN1 component of this response, appearing about 170 ms after motion onset, was two times higher in amplitude for blind compared with matched sighted control subjects. At the time of the cN1, electrical neuroimaging using sLORETA revealed stronger activation in blind than sighted subjects primarily in ventral visual

areas (V1v, V2v, VP, V4v) of the right occipital lobe. Activation was also obtained in middle temporal area V5. These findings suggest that blindness results in stronger involvement of both non-motion areas of the ventral visual stream and motion areas of the dorsal visual stream in processing of auditory motion at the same point in time after motion onset. This argues against the Mdm2 inhibitor view that visual motion areas, Aspartate such as area V5, are preferentially recruited

for auditory motion analysis in the blind. Rather, cross-modal reorganization of cortical areas induced by blindness seems to be largely independent of the specific visual functions of the same areas in sighted persons. “
“Replication and segregation of genetic information are the activities central to the well-being of all living cells. Concerted mechanisms have evolved that ensure that each cellular chromosome is replicated once and only once per cell cycle and then faithfully segregated into daughter cells. Despite remarkable taxonomic diversity, these mechanisms are largely conserved across eubacteria, although species-specific distinctions can often be noted. Here, we provide an overview of the current state of knowledge about maintenance of the chromosome structure in Pseudomonas aeruginosa. We focus on global chromosome organization and its dynamics during DNA replication and cell division. Special emphasis is made on contrasting these activities in P. aeruginosa and other bacteria. Among unique P. aeruginosa, features are the presence of two distinct autonomously replicating sequences and multiple condensins, which suggests existence of novel regulatory mechanisms.