In Vivo Localization of Fas-Associated Death Domain Protein in the Nucleus and Cytoplasm of Normal Thyroid and Liver Cells

FADD (Fas-associated death domain) is the main death receptor adaptor molecule that transmits apoptotic signal. Recently, FADD protein was shown to be expressed both in the cytoplasm and nucleus of in vitro cell lines. In contrast to the cytoplasmic FADD, the nuclear FADD was shown to protect cells from apoptosis. However, in vivo subcellular localization of FADD was still unknown. Here, we demonstrated that FADD protein was expressed in both cytoplasmic and nuclear compartment in ex vivo thyroid cells demonstrating that nuclear sublocalization of FADD protein was a relevant phenomenon occurring in vivo. Moreover, we showed that in the nucleus of untransformed thyroid cells FADD localized mainly on euchromatin. We confirmed the nuclear localization of FADD in ex vivo liver and showed that in this organ FADD and MBD4 interact together. These results demonstrate that FADD is physiologically expressed in the nucleus of cells in at least two mouse organs. This particular localization opens new possible role of FADD in vivo either asan inhibitor of cell death, or as a transcription factor, or as a molecular link between apoptosis and genome surveillance

Electron-Lattice Interplays in LaMnO3 from Canonical Jahn-Teller Distortion Notations

LaMnO$_3$ is considered as a prototypical Jahn-Teller perovskite compound, exhibiting a metal to insulator transition at $T_{JT} = 750K$ related to the joint appearance of an electronic orbital ordering and a large lattice Jahn-Teller distortion. From first-principles, we revisit the behavior of LaMnO$_3$ and show that it is not only prone to orbital ordering but also to charge ordering. Both charge and orbital orderings appear to be enabled by rotations of the oxygen octahedra and the subtle competition between them is monitored by a large tetragonal compressive strain, that is itself a Jahn-Teller active distortion. Equally, the competition of ferromagnetic and antiferromagnetic orders is slave of the same tetragonal strain. Our results further indicate that the metal to insulator transition can be thought as a Peierls transition that is enabled by spin symmetry breaking. Therefore, dynamical spin fluctuations in the paramagnetic state stabilize the insulating phase by the instantaneous symmetry breaking they produce and which is properly captured from static DFT calculations. As a basis to our discussion, we introduce canonical notations for lattice distortions in perovskites that distort the oxygen octhedra and are connected to charge and orbital orderings

La motte castrale de Guéramé à Courgains (Sarthe), aux confins du Maine et du Perche

Une opération de diagnostic réalisée en 2006 sur la commune de Courgains dans le nord de la Sarthe a permis de confirmer la présence d’une motte et de sa basse-cour, site découvert en prospection aérienne en 1999 par G. Leroux (INRAP). Le gisement, baptisé « Guéramé » par son inventeur, est d’abord constitué d’un fossé de 7 à 8 m de largeur et de presque 2,50 m de profondeur. Il entoure une plate-forme circulaire de 20 m de diamètre. Aujourd’hui, le relief de la motte ainsi enserrée est presq..

A short motif in Drosophila SECIS Binding Protein 2 provides differential binding affinity to SECIS RNA hairpins

Selenoproteins contain the amino acid selenocysteine which is encoded by a UGA Sec codon. Recoding UGA Sec requires a complex mechanism, comprising the cis-acting SECIS RNA hairpin in the 3′UTR of selenoprotein mRNAs, and trans-acting factors. Among these, the SECIS Binding Protein 2 (SBP2) is central to the mechanism. SBP2 has been so far functionally characterized only in rats and humans. In this work, we report the characterization of the Drosophila melanogaster SBP2 (dSBP2). Despite its shorter length, it retained the same selenoprotein synthesis-promoting capabilities as the mammalian counterpart. However, a major difference resides in the SECIS recognition pattern: while human SBP2 (hSBP2) binds the distinct form 1 and 2 SECIS RNAs with similar affinities, dSBP2 exhibits high affinity toward form 2 only. In addition, we report the identification of a K (lysine)-rich domain in all SBP2s, essential for SECIS and 60S ribosomal subunit binding, differing from the well-characterized L7Ae RNA-binding domain. Swapping only five amino acids between dSBP2 and hSBP2 in the K-rich domain conferred reversed SECIS-binding properties to the proteins, thus unveiling an important sequence for form 1 binding

GYY4137-Derived Hydrogen Sulfide Donates Electrons to the Mitochondrial Electron Transport Chain via Sulfide:Quinone Oxidoreductase in Endothelial Cells

The protective effects of hydrogen sulphide (H2S) to limit oxidative injury and preserve mitochondrial function during sepsis, ischemia/reperfusion, and neurodegenerative diseases have prompted the development of soluble H2S-releasing compounds such as GYY4137. Yet, the effects of GYY4137 on the mitochondrial function of endothelial cells remain unclear, while this cell type comprises the first target cell after parenteral administration. Here, we specifically assessed whether human endothelial cells possess a functional sulfide:quinone oxidoreductase (SQOR), to oxidise GYY4137-released H2S within the mitochondria for electron donation to the electron transport chain. We demonstrate that H2S administration increases oxygen consumption by human umbilical vein endothelial cells (HUVECs), which does not occur in the SQOR-deficient cell line SH-SY5Y. GYY4137 releases H2S in HUVECs in a dose- and time-dependent fashion as quantified by oxygen consumption and confirmed by lead acetate assay, as well as AzMC fluorescence. Scavenging of intracellular H2S using zinc confirmed intracellular and intramitochondrial sulfur, which resulted in mitotoxic zinc sulfide (ZnS) precipitates. Together, GYY4137 increases intramitochondrial H2S and boosts oxygen consumption of endothelial cells, which is likely governed via the oxidation of H2S by SQOR. This mechanism in endothelial cells may be instrumental in regulating H2S levels in blood and organs but can also be exploited to quantify H2S release by soluble donors such as GYY4137 in living systems.</p

From charge- to orbital-ordered metal-insulator transition in alkaline-earth ferrites

While CaFeO3 exhibits upon cooling a metal-insulator transition linked to charge ordering, SrFeO3 and BaFeO3 keep metallic behaviors down to very low temperatures. Moreover, alkaline-earth ferrites do not seem prone to orbital ordering in spite of the d4 formal occupancy of Fe4+. Here, from first-principles simulations, we show that the metal-insulator transition of CaFeO3 is structurally triggered by oxygen rotation motions as in rare-earth nickelates. This not only further clarifies why SrFeO3 and BaFeO3 remain metallic but allows us to predict that an insulating charge-ordered phase can be induced in SrFeO3 from an appropriate engineering of oxygen rotation motions. Going further, we unveil the possibility to switch from the usual charge-ordered to an orbital-ordered insulating ground state under moderate tensile strain in CaFeO3 thin films. We rationalize the competition between charge and orbital orderings, highlighting alternative possible strategies to produce such a change of ground state, also relevant to manganite and nickelate compounds. © 2018 American Physical Society

The XUV environments of exoplanets from Jupiter-size to super-Earth

Planets that reside close-in to their host star are subject to intense high-energy irradiation. Extreme-ultraviolet (EUV) and X-ray radiation (together, XUV) is thought to drive mass-loss from planets with volatile envelopes. We present XMM–Newton observations of six nearby stars hosting transiting planets in tight orbits (with orbital period, Porb < 10 d), wherein we characterize the XUV emission from the stars and subsequent irradiation levels at the planets. In order to reconstruct the unobservable EUV emission, we derive a new set of relations from Solar TIMED/SEE data that are applicable to the standard bands of the current generation of X-ray instruments. From our sample, WASP-80b and HD 149026b experience the highest irradiation level, but HAT-P-11b is probably the best candidate for Ly α evaporation investigations because of the system’s proximity to the Solar system. The four smallest planets have likely lost a greater percentage of their mass over their lives than their larger counterparts. We also detect the transit of WASP-80b in the near-ultraviolet with the optical monitor on XMM–Newton

<i>TBC1D8B </i>Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways

International audienceSteroid-resistant nephrotic syndrome (SRNS) is characterized by high-range proteinuria and most often focal and segmental glomerulosclerosis (FSGS). Identification of mutations in genes causing SRNS has improved our understanding of disease mechanisms and highlighted defects in the podocyte, a highly specialized glomerular epithelial cell, as major factors in disease pathogenesis. By exome sequencing, we identified missense mutations in TBC1D8B in two families with an X-linked early-onset SRNS with FSGS. TBC1D8B is an uncharacterized Rab-GTPase-activating protein likely involved in endocytic and recycling pathways. Immunofluorescence studies revealed TBC1D8B presence in human glomeruli, and affected individual podocytes displayed architectural changes associated with migration defects commonly found in FSGS. In zebrafish we demonstrated that both knockdown and knockout of the unique TBC1D8B ortholog-induced proteinuria and that this phenotype was rescued by human TBC1D8B mRNA injection, but not by either of the two mutated mRNAs. We also showed an interaction between TBC1D8B and Rab11b, a key protein in vesicular recycling in cells. Interestingly, both internalization and recycling processes were dramatically decreased in affected individuals' podocytes and fibroblasts, confirming the crucial role of TBC1D8B in the cellular recycling processes, probably as a Rab11b GTPase-activating protein. Altogether, these results confirmed that pathogenic variations in TBC1D8B are involved in X-linked podocytopathy and points to alterations in recycling processes as a mechanism of SRNS