p53 isoforms change p53 paradigm

Although p53 defines cellular responses to cancer treatment it is not clear how p53 can be used to control cell fate outcome. Data demonstrate that so-called p53 does not exist as a single protein, but is in fact a group of p53 protein isoforms whose expression can be manipulated to control the cellular response to treatment

Scotin, a novel p53-inducible proapoptotic protein located in the ER and the nuclear membrane

p53 is a transcription factor that induces growth arrest or apoptosis in response to cellular stress. To identify new p53-inducible proapoptotic genes, we compared, by differential display, the expression of genes in spleen or thymus of normal and p53 nullizygote mice after γ-irradiation of whole animals. We report the identification and characterization of human and mouse Scotin homologues, a novel gene directly transactivated by p53. The Scotin protein is localized to the ER and the nuclear membrane. Scotin can induce apoptosis in a caspase-dependent manner. Inhibition of endogenous Scotin expression increases resistance to p53-dependent apoptosis induced by DNA damage, suggesting that Scotin plays a role in p53-dependent apoptosis. The discovery of Scotin brings to light a role of the ER in p53-dependent apoptosis

Conformal dimension and random groups

We give a lower and an upper bound for the conformal dimension of the boundaries of certain small cancellation groups. We apply these bounds to the few relator and density models for random groups. This gives generic bounds of the following form, where $l$ is the relator length, going to infinity. (a) 1 + 1/C < \Cdim(\bdry G) < C l / \log(l), for the few relator model, and (b) 1 + l / (C\log(l)) < \Cdim(\bdry G) < C l, for the density model, at densities $d < 1/16$. In particular, for the density model at densities $d < 1/16$, as the relator length $l$ goes to infinity, the random groups will pass through infinitely many different quasi-isometry classes.Comment: 32 pages, 4 figures. v2: Final version. Main result improved to density < 1/16. Many minor improvements. To appear in GAF

Unital quantum operators on the Bloch ball and Bloch region

For one qubit systems, we present a short, elementary argument characterizing unital quantum operators in terms of their action on Bloch vectors. We then show how our approach generalizes to multi-qubit systems, obtaining inequalities that govern when a ``diagonal'' superoperator on the Bloch region is a quantum operator. These inequalities are the n-qubit analogue of the Algoet-Fujiwara conditions. Our work is facilitated by an analysis of operator-sum decompositions in which negative summands are allowed.Comment: Revised and corrected, to appear in Physical Review

Effect of Maturation on Hemodynamic and Autonomic Control Recovery Following Maximal Running Exercise in Highly Trained Young Soccer Players

The purpose of this study was to examine the effect of maturation on post-exercise hemodynamic and autonomic responses. Fifty-five highly trained young male soccer players (12–18 years) classified as pre-, circum-, or post-peak height velocity (PHV) performed a graded running test to exhaustion on a treadmill. Before (Pre) and after (5th–10th min, Post) exercise, heart rate (HR), stroke volume (SV), cardiac output (CO), arterial pressure (AP), and total peripheral resistance (TPR) were monitored. Parasympathetic (high frequency [HFRR] of HR variability (HRV) and baroreflex sensitivity [Ln BRS]) and sympathetic activity (low frequency [LFSAP] of systolic AP variability) were estimated. Post-exercise blood lactate [La]b, the HR recovery (HRR) time constant, and parasympathetic reactivation (time-varying HRV analysis) were assessed. In all three groups, exercise resulted in increased HR, CO, AP, and LFSAP (P < 0.001), decreased SV, HFRR, and Ln BRS (all P < 0.001), and no change in TPR (P = 0.98). There was no “maturation × time” interaction for any of the hemodynamic or autonomic variables (all P > 0.22). After exercise, pre-PHV players displayed lower SV, CO, and [La]b, faster HRR and greater parasympathetic reactivation compared with circum- and post-PHV players. Multiple regression analysis showed that lean muscle mass, [La]b, and Pre parasympathetic activity were the strongest predictors of HRR (r2 = 0.62, P < 0.001). While pre-PHV players displayed a faster HRR and greater post-exercise parasympathetic reactivation, maturation had little influence on the hemodynamic and autonomic responses following maximal running exercise. HRR relates to lean muscle mass, blood acidosis, and intrinsic parasympathetic function, with less evident impact of post-exercise autonomic function

A laser triggered electron source for pulsed radiolysis

We present the design of a photo-injector based accelerator for pulsed radiolysis applications. This machine is destined to meet the needs of the physical chemistry community at the Universite de Paris XI. A 4 MeV Energy electron pulse of a few picoseconds duration and with a charge in the range of 1 to 10 nC is produced from a Cs/sub 2 /Te photocathode. The photocathode is placed in the half energy spread cell of a 1-1/2 cell, 3 GHz RF gun, whose design is based on the gun used for the drive beam of the CERN CLIC Test facility. A 4 cell "booster" cavity is then used to accelerate the beam to an energy of 9 MeV. The transport system consists of a quadrupole triplet downsteam of the booster, two rectangular, 30 degree bend, dipoles with a pair of quadrupoles between them and a second triplet downstream of the second dipole. Energy dependent path length effects in the two dipoles allow the possibility of magnetic bunch compression depending on the phase-energy correlation of the bunch exiting the booster cavity. The beam envelope and the bunch length have been calculated through the transport line using TRACE-3d and PARMELA. These codes allow us to verify the required beam parameters at the experimental areas. We discuss the adjustment of the optics, aimed at producing the minimum electron bunch length at the experimental targets. (4 refs)

Toward systems biology in brown algae to explore acclimation and adaptation to the shore environment.

International audienceBrown algae belong to a phylogenetic lineage distantly related to land plants and animals. They are almost exclusively found in the intertidal zone, a harsh and frequently changing environment where organisms are submitted to marine and terrestrial constraints. In relation with their unique evolutionary history and their habitat, they feature several peculiarities, including at the level of their primary and secondary metabolism. The establishment of Ectocarpus siliculosus as a model organism for brown algae has represented a framework in which several omics techniques have been developed, in particular, to study the response of these organisms to abiotic stresses. With the recent publication of medium to high throughput profiling data, it is now possible to envision integrating observations at the cellular scale to apply systems biology approaches. As a first step, we propose a protocol focusing on integrating heterogeneous knowledge gained on brown algal metabolism. The resulting abstraction of the system will then help understanding how brown algae cope with changes in abiotic parameters within their unique habitat, and to decipher some of the mechanisms underlying their (1) acclimation and (2) adaptation, respectively consequences of (1) the behavior or (2) the topology of the system resulting from the integrative approach

Weighted composition operators on Korenblum type spaces of analytic functions

[EN] We investigate the continuity, compactness and invertibility of weighted composition operators W-psi,W-phi: f -> psi(f circle phi) when they act on the classical Korenblum space A(-infinity) and other related Frechet or (LB)-spaces of analytic functions on the open unit disc which are defined as intersections or unions of weighted Banach spaces with sup-norms. Some results about the spectrum of these operators are presented in case the self-map phi has a fixed point in the unit disc. A precise description of the spectrum is obtained in this case when the operator acts on the Korenblum space.This research was partially supported by the research project MTM2016-76647-P and the grant BES-2017-081200.Gomez-Orts, E. (2020). Weighted composition operators on Korenblum type spaces of analytic functions. Revista de la Real Academia de Ciencias Exactas Físicas y Naturales Serie A Matemáticas. 114(4):1-15. https://doi.org/10.1007/s13398-020-00924-1S1151144Abramovich, Y.A., Aliprantis, C.D.: An invitation to operator theory. Graduate Studies in Mathematics. Amer. Math. Soc., 50 (2002)Albanese, A.A., Bonet, J., Ricker, W.J.: The Cesàro operator in the Fréchet spaces $$\ell ^{p+}$$ and $$L^{p-}$$. Glasgow Math. J. 59, 273–287 (2017)Albanese, A.A., Bonet, J., Ricker, W.J.: The Cesàro operator on Korenblum type spaces of analytic functions. Collect. Math. 69(2), 263–281 (2018)Albanese, A.A., Bonet, J., Ricker, W.J.: Operators on the Fréchet sequence spaces $$ces(p+), 1\le p\le \infty$$. Rev. R. Acad. Cienc. Exactas Fís. Nat. Ser. A Mat. RACSAM 113(2), 1533–1556 (2019)Albanese, A.A., Bonet, J., Ricker, W.J.: Linear operators on the (LB)-sequence spaces $$ces(p-), 1\le p\le \infty$$. Descriptive topology and functional analysis. II, 43–67, Springer Proc. Math. Stat., 286, Springer, Cham (2019)Arendt, W., Chalendar, I., Kumar, M., Srivastava, S.: Powers of composition operators: asymptotic behaviour on Bergman, Dirichlet and Bloch spaces. J. Austral. Math. Soc. 1–32. https://doi.org/10.1017/S1446788719000235Aron, R., Lindström, M.: Spectra of weighted composition operators on weighted Banach spaces of analytic funcions. Israel J. Math. 141, 263–276 (2004)Bierstedt, K.D., Summers, W.H.: Biduals of weighted Banach spaces of analytic functions. J. Austral. Math. Soc., Ser. A, 54(1), 70–79 (1993)Bonet, J.: A note about the spectrum of composition operators induced by a rotation. RACSAM 114, 63 (2020). https://doi.org/10.1007/s13398-020-00788-5Bonet, J., Domański, P., Lindström, M., Taskinen, J.: Composition operators between weighted Banach spaces of analytic functions. J. Austral. Math. Soc., Ser. A, 64(1), 101–118 (1998)Bourdon, P.S.: Essential angular derivatives and maximum growth of Königs eigenfunctions. J. Func. Anal. 160, 561–580 (1998)Bourdon, P.S.: Invertible weighted composition operators. Proc. Am. Math. Soc. 142(1), 289–299 (2014)Carleson, L., Gamelin, T.: Complex Dynamics. Springer, Berlin (1991)Cowen, C., MacCluer, B.: Composition Operators on Spaces of Analytic Functions. CRC Press, Boca Raton, FL (1995)Contreras, M., Hernández-Díaz, A.G.: Weighted composition operators in weighted Banach spacs of analytic functions. J. Austral. Math. Soc., Ser. A 69, 41–60 (2000)Eklund, T., Galindo, P., Lindström, M.: Königs eigenfunction for composition operators on Bloch and $$H^\infty$$ spaces. J. Math. Anal. Appl. 445, 1300–1309 (2017)Hedenmalm, H., Korenblum, B., Zhu, K.: Theory of Bergman Spaces. Grad. Texts in Math. 199. Springer, New York (2000)Jarchow, H.: Locally Convex Spaces. Teubner, Stuttgart (1981)Kamowitz, H.: Compact operators of the form $$uC_{\varphi }$$. Pac. J. Math. 80(1) (1979)Korenblum, B.: An extension of the Nevanlinna theory. Acta Math. 135, 187–219 (1975)Köthe, G.: Topological Vector Spaces II. Springer, New York Inc (1979)Lusky, W.: On the isomorphism classes of weighted spaces of harmonic and holomophic functions. Stud. Math. 75, 19–45 (2006)Meise, R., Vogt, D.: Introduction to functional analysis. Oxford Grad. Texts in Math. 2, New York, (1997)Montes-Rodríguez, A.: Weighted composition operators on weighted Banach spaces of analytic functions. J. Lond. Math. Soc. 61(3), 872–884 (2000)Queffélec, H., Queffélec, M.: Diophantine Approximation and Dirichlet series. Hindustain Book Agency, New Delhi (2013)Shapiro, J.H.: Composition Operators and Classical Function Theory. Springer, New York (1993)Shields, A.L., Williams, D.L.: Bounded projections, duality and multipliers in spaces of analytic functions. Trans. Amer. Math. Soc. 162, 287–302 (1971)Zhu, K.: Operator Theory on Function Spaces, Math. Surveys and Monographs, Amer. Math. Soc. 138 (2007

Southern Ocean control of silicon stable isotope distribution in the deep Atlantic Ocean

Author Posting. © American Geophysical Union, 2012. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Geochemical Cycles 26 (2012): GB2035, doi:10.1029/2011GB004141.The fractionation of silicon (Si) stable isotopes by biological activity in the surface ocean makes the stable isotope composition of silicon (δ30Si) dissolved in seawater a sensitive tracer of the oceanic biogeochemical Si cycle. We present a high-precision dataset that characterizes the δ30Si distribution in the deep Atlantic Ocean from Denmark Strait to Drake Passage, documenting strong meridional and smaller, but resolvable, vertical δ30Si gradients. We show that these gradients are related to the two sources of deep and bottom waters in the Atlantic Ocean: waters of North Atlantic and Nordic origin carry a high δ30Si signature of ≥+1.7‰ into the deep Atlantic, while Antarctic Bottom Water transports Si with a low δ30Si value of around +1.2‰. The deep Atlantic δ30Si distribution is thus governed by the quasi-conservative mixing of Si from these two isotopically distinct sources. This disparity in Si isotope composition between the North Atlantic and Southern Ocean is in marked contrast to the homogeneity of the stable nitrogen isotope composition of deep ocean nitrate (δ15N-NO3). We infer that the meridional δ30Si gradient derives from the transport of the high δ30Si signature of Southern Ocean intermediate/mode waters into the North Atlantic by the upper return path of the meridional overturning circulation (MOC). The basin-scale deep Atlantic δ30Si gradient thus owes its existence to the interaction of the physical circulation with biological nutrient uptake at high southern latitudes, which fractionates Si isotopes between the abyssal and intermediate/mode waters formed in the Southern Ocean.This work was supported by Swiss National Science Foundation grants 200021-116473 and 200020-130361.2012-12-1