82 research outputs found

    The Mother Tongue of Love and Loss:Albert Cohen’s Le Livre de ma mère

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    This article reads Albert Cohen’s Le Livre de ma mère, which mourns the death of his mother, as a poetics of love and loss. It is a poetics of otherness that disavows the claim to expression and selfhood. The mother, being the paradigmatic figure of otherness, is a figure for literature, a form of language that is characterized by saying things differently. Literature itself is a motherly space insofar as it others the language of the self. This argument is developed along close readings of both the French original and the English translation of Cohen’s work, following three thematic axes: first, the peculiar kinship of love and death; second, the mother as the other; third, literature as filio-logy: a logic of filiation that does not leave the self unchanged.Caroline Sauter, ‘The Mother Tongue of Love and Loss: Albert Cohen’s **Le Livre de ma mère/**’, in Untying the Mother Tongue, ed. by Antonio Castore and Federico Dal Bo, Cultural Inquiry, 26 (Berlin: ICI Berlin Press, 2023), pp. 165-79 <https://doi.org/10.37050/ci-26_8

    Performance individuelle au sein d'une équipe d'étudiants entrepreneurs : en quoi l'équipe influence-t-elle la capacité d'agir de ses membres ?

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    International audienceThis research studies a postgraduate programme whose pedagogy is based on experiential learning approach, work and team learning. Based on self-determination theory of Deci & Ryan (1985), the study highlights and describes how the team impacts motivation for action of its members.Cette recherche étudie un dispositif universitaire dont la pédagogie est fondée sur l'apprentissage par action, travail et apprentissage en équipe. En s'appuyant sur la théorie de l'auto-détermination de Deci et Ryan (1985) l'étude met en évidence et décrit la manière dont l'équipe impacte la motivation à agir de ses membres

    Deinococcus glutaminyl-tRNA synthetase is a chimer between proteins from an ancient and the modern pathways of aminoacyl-tRNA formation

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    Glutaminyl-tRNA synthetase from Deinococcus radiodurans possesses a C-terminal extension of 215 residues appending the anticodon-binding domain. This domain constitutes a paralog of the Yqey protein present in various organisms and part of it is present in the C-terminal end of the GatB subunit of GatCAB, a partner of the indirect pathway of Gln-tRNA(Gln) formation. To analyze the peculiarities of the structure–function relationship of this GlnRS related to the Yqey domain, a structure of the protein was solved from crystals diffracting at 2.3 Å and a docking model of the synthetase complexed to tRNA(Gln) constructed. The comparison of the modeled complex with the structure of the E. coli complex reveals that all residues of E. coli GlnRS contacting tRNA(Gln) are conserved in D. radiodurans GlnRS, leaving the functional role of the Yqey domain puzzling. Kinetic investigations and tRNA-binding experiments of full length and Yqey-truncated GlnRSs reveal that the Yqey domain is involved in tRNA(Gln) recognition. They demonstrate that Yqey plays the role of an affinity-enhancer of GlnRS for tRNA(Gln) acting only in cis. However, the presence of Yqey in free state in organisms lacking GlnRS, suggests that this domain may exert additional cellular functions

    Assessment of modulated hot wire method for thermophysical characterization of fluid and solid matrices charged with (nano)particle inclusions

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    Recently we reported on simultaneous thermal conductivity k and thermal diffusivity a measurement of liquids and in particular of nanofluids in a configuration using an ac excited hot wire combined with lock-in detection of the third harmonic (3ω method) [1]. The conductive wire is used as both heater and sensor. The requirements for the asymptotic validity of the line heat source model are fulfilled at low modulation frequencies below a few Hz. The study of the relative sensitivity of signal amplitude and phase to changes in k and a indicates that there is an optimum frequency range for accurate and stable results. We extend by up to two decades the feasible frequency range for 3ω measurements by considering various more elaborate models for the heat transfer between the wire and the fluid. Finally we show that the same ac hot wire method can be applied to soft solid, composite materials. We measured the k enhancement of a poly(ethylene vinyl acetate) EVA polymer matrix charged with various fractions of graphite

    Pre-verbal infants perceive emotional facial expressions categorically

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    Adults perceive emotional expressions categorically, with discrimination being faster and more accurate between expressions from different emotion categories (i.e. blends with two different predominant emotions) than between two stimuli from the same category (i.e. blends with the same predominant emotion). The current study sought to test whether facial expressions of happiness and fear are perceived categorically by pre-verbal infants, using a new stimulus set that was shown to yield categorical perception in adult observers (Experiments 1 and 2). These stimuli were then used with 7-month-old infants (N  =  34) using a habituation and visual preference paradigm (Experiment 3). Infants were first habituated to an expression of one emotion, then presented with the same expression paired with a novel expression either from the same emotion category or from a different emotion category. After habituation to fear, infants displayed a novelty preference for pairs of between-category expressions, but not within-category ones, showing categorical perception. However, infants showed no novelty preference when they were habituated to happiness. Our findings provide evidence for categorical perception of emotional expressions in pre-verbal infants, while the asymmetrical effect challenges the notion of a bias towards negative information in this age group

    Reappraisal of the magma-rich versus magma-poor rifted margin archetypes

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    Abstract Rifted margins are commonly defined as magma-poor or magma-rich archetypes based on their morphology. We re-examine the prevailing model inferred from this classification that magma-rich margins have excess decompression melting at lithospheric breakup compared with steady-state seafloor spreading, while magma-poor margins have inhibited melting. We investigate the magmatic budget related to lithospheric breakup along two high-resolution long-offset deep reflection seismic profiles across the SE Indian (magma-poor) and Uruguayan (magma-rich) rifted margins. Resolving the magmatic budget is difficult and several interpretations can explain our seismic observations, implying different mechanisms to achieve lithospheric breakup and melt production for each archetype. We show that the Uruguayan and other magma-rich margins may indeed involve excess decompression melting compared with steady-state seafloor spreading but could also be explained by a gradual increase with an early onset relative to crustal breakup. A late onset of decompression melting relative to crustal breakup enables mantle exhumation characteristic of magma-poor margin archetypes (e.g. SE India). Despite different volumes of magmatism, the mechanisms suggested at lithospheric breakup are comparable between both archetypes. Considerations on the timing of decompression melting onset relative to crustal thinning may be more important than the magmatic budget to understand the evolution and variability of rifted margins.</jats:p

    PITX1 is a regulator of TERT expression in prostate cancer with prognostic power

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    Simple Summary Most prostate cancer is of an indolent form and is curable. However, some prostate cancer belongs to rather aggressive subtypes leading to metastasis and death, and immediate therapy is mandatory. However, for these, the therapeutic options are highly invasive, such as radical prostatectomy, radiation or brachytherapy. Hence, a precise diagnosis of these tumor subtypes is needed, and the thus far applied diagnostic means are insufficient for this. Besides this, for their endless cell divisions, prostate cancer cells need the enzyme telomerase to elongate their telomeres (chromatin endings). In this study, we developed a gene regulatory model based on large data from transcription profiles from prostate cancer and chromatin-immuno-precipitation studies. We identified the developmental regulator PITX1 regulating telomerase. Besides observing experimental evidence of PITX1′s functional role in telomerase regulation, we also found PITX1 serving as a prognostic marker, as concluded from an analysis of more than 15,000 prostate cancer samples. Abstract The current risk stratification in prostate cancer (PCa) is frequently insufficient to adequately predict disease development and outcome. One hallmark of cancer is telomere maintenance. For telomere maintenance, PCa cells exclusively employ telomerase, making it essential for this cancer entity. However, TERT, the catalytic protein component of the reverse transcriptase telomerase, itself does not suit as a prognostic marker for prostate cancer as it is rather low expressed. We investigated if, instead of TERT , transcription factors regulating TERT may suit as prognostic markers. To identify transcription factors regulating TERT , we developed and applied a new gene regulatory modeling strategy to a comprehensive transcriptome dataset of 445 primary PCa. Six transcription factors were predicted as TERT regulators, and most prominently, the developmental morphogenic factor PITX1. PITX1 expression positively correlated with telomere staining intensity in PCa tumor samples. Functional assays and chromatin immune-precipitation showed that PITX1 activates TERT expression in PCa cells. Clinically, we observed that PITX1 is an excellent prognostic marker, as concluded from an analysis of more than 15,000 PCa samples. PITX1 expression in tumor samples associated with (i) increased Ki67 expression indicating increased tumor growth, (ii) a worse prognosis, and (iii) correlated with telomere length

    Loss of Ambra1 promotes melanoma growth and invasion

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    Melanoma is the deadliest skin cancer. Despite improvements in the understanding of the molecular mechanisms underlying melanoma biology and in defining new curative strategies, the therapeutic needs for this disease have not yet been fulfilled. Herein, we provide evidence that the Activating Molecule in Beclin-1-Regulated Autophagy (Ambra1) contributes to melanoma development. Indeed, we show that Ambra1 deficiency confers accelerated tumor growth and decreased overall survival in Braf/Pten-mutated mouse models of melanoma. Also, we demonstrate that Ambra1 deletion promotes melanoma aggressiveness and metastasis by increasing cell motility/invasion and activating an EMT-like process. Moreover, we show that Ambra1 deficiency in melanoma impacts extracellular matrix remodeling and induces hyperactivation of the focal adhesion kinase 1 (FAK1) signaling, whose inhibition is able to reduce cell invasion and melanoma growth. Overall, our findings identify a function for AMBRA1 as tumor suppressor in melanoma, proposing FAK1 inhibition as a therapeutic strategy for AMBRA1 low-expressing melanoma. The absence of scaffold protein Ambra1 leads to hyperproliferation and growth in mouse models. Here the authors show that Ambra1 deficiency accelerates melanoma growth and increases metastasis in mouse models of melanoma through FAK1 hyperactivation

    Natural Killer Cell Education Is Associated With a Distinct Glycolytic Profile

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    NK cells expressing self-inhibitory receptors display increased functionality compared to NK cells lacking those receptors. The acquisition of functional competence in these particular NK-cell subsets is termed education. Little is known about the underlying mechanisms that lead to the functional differences between educated and uneducated NK cells. An increasing number of studies suggest that cellular metabolism is a determinant of immune cell functions. Thus, alterations in cellular metabolic pathways may play a role in the process of NK-cell education. Here, we compared the glycolytic profile of educated and uneducated primary human NK cells. KIR-educated NK cells showed significantly increased expression levels of the glucose transporter Glut1 in comparison to NKG2A-educated or uneducated NK cells with and without exposure to target cells. Subsequently, the metabolic profile of NK-cell subsets was determined using a Seahorse XF Analyzer. Educated NK cells displayed significantly higher rates of cellular glycolysis than uneducated NK cells even in a resting state. Our results indicate that educated and uneducated NK cells reside in different metabolic states prior to activation. These differences in the ability to utilize glucose may represent an underlying mechanism for the superior functionality of educated NK cells expressing self-inhibitory receptors
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