76 research outputs found

    Review submerged speleothems and sea level reconstructions: A global overview and new results from the mediterranean sea

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    This study presents a global overview of the submerged speleothems used to reconstruct paleo sea levels and reports new results from two stalactites collected in the Mediterranean Sea. Coastal cave deposits significantly contributed to the understanding of global and regional sea-level variations during the Middle and Late Quaternary. The studied speleothems cover the last 1.4 Myr and focused mainly on Marine Isotope Stages (MIS) 1, 2, 3, 5.1, 5.3, 5.5, 7.1, 7.2, 7.3 and 7.5. The results indicate that submerged speleothems represent extraordinary archives that can provide detailed information on former sea-level changes. The two stalactites collected in the central Mediterranean Sea, at Favignana and Ustica islands (Sicily, Italy), are both characterized by continental, phreatic or marine layers. The U-Th and14C ages of the new speleothems provide results of great interest for relative sea-level changes over the last 1000 years

    The host metabolite D-serine contributes to bacterial niche specificity through gene selection

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    Escherichia coli comprise a diverse array of both commensals and niche-specific pathotypes. The ability to cause disease results from both carriage of specific virulence factors and regulatory control of these via environmental stimuli. Moreover, host metabolites further refine the response of bacteria to their environment and can dramatically affect the outcome of the host–pathogen interaction. Here, we demonstrate that the host metabolite, D-serine, selectively affects gene expression in E. coli O157:H7. Transcriptomic profiling showed exposure to D-serine results in activation of the SOS response and suppresses expression of the Type 3 Secretion System (T3SS) used to attach to host cells. We also show that concurrent carriage of both the D-serine tolerance locus (dsdCXA) and the locus of enterocyte effacement pathogenicity island encoding a T3SS is extremely rare, a genotype that we attribute to an ‘evolutionary incompatibility’ between the two loci. This study demonstrates the importance of co-operation between both core and pathogenic genetic elements in defining niche specificity

    Phosphatase and tensin homologue: a therapeutic target for SMA

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    Spinal muscular atrophy (SMA) is one of the most common juvenile neurodegenerative diseases, which can be associated with child mortality. SMA is caused by a mutation of ubiquitously expressed gene, Survival Motor Neuron1 (SMN1), leading to reduced SMN protein and the motor neuron death. The disease is incurable and the only therapeutic strategy to follow is to improve the expression of SMN protein levels in motor neurons. Significant numbers of motor neurons in SMA mice and SMA cultures are caspase positive with condensed nuclei, suggesting that these cells are prone to a process of cell death called apoptosis. Searching for other potential molecules or signaling pathways that are neuroprotective for central nervous system (CNS) insults is essential for widening the scope of developmental medicine. PTEN, a Phosphatase and Tensin homologue, is a tumor suppressor, which is widely expressed in CNS. PTEN depletion activates anti-apoptotic factors and it is evident that the pathway plays an important protective role in many neurodegenerative disorders. It functions as a negative regulator of PIP3/AKT pathway and thereby modulates its downstream cellular functions through lipid phosphatase activity. Moreover, previous reports from our group demonstrated that, PTEN depletion using viral vector delivery system in SMN delta7 mice reduces disease pathology, with significant rescue on survival rate and the body weight of the SMA mice. Thus knockdown/depletion/mutation of PTEN and manipulation of PTEN medicated Akt/PKB signaling pathway may represent an important therapeutic strategy to promote motor neuron survival in SMA

    Experimental and theoretical studies of intergranular strain in an alpha titanium alloy during plastic deformation

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    International audienceTwo complementary methods were used to analyse the deformation mechanisms involved in the plasticity of commercially pure titanium during compressive loading: neutron diffraction and the self-consistent model. The strain response of 15 crystallographic planes was tracked during the measurement, in directions both parallel and transverse to the straining direction, providing new insight into the mechanical behaviour of the polycrystal. The neutron diffraction results show evidence of tensile twins in the titanium alloy studied. The twin volume fraction was determined from the change in crystallographic texture. The influence and the role of plastic anisotropy were also studied and explained in this work. Good agreement was found between the experimental and predicted results

    French round-robin test of X-ray stress determination on a shot-peened steel

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