Keck and ESO-VLT View of the Symmetry of the Ejecta of the XRF/SN 2006aj

Nebular-phase spectra of SN 2006aj, which was discovered in coincidence with X-ray flash 060218, were obtained with Keck in 2006 July and the Very Large Telescope in 2006 September. At the latter epoch spectropolarimetry was also attempted, yielding an upper limit of ~ 2% for the polarization. The spectra show strong emission lines of [OI] and MgI], as expected from a Type Ic supernova, but weak CaII lines. The [FeII] lines that were strong in the spectra of SN 1998bw are much weaker in SN 2006aj, consistent with the lower luminosity of this SN. The outer velocity of the line-emitting ejecta is ~ 8000 km/s in July and ~ 7400 km/s in September, consistent with the relatively low kinetic energy of expansion of SN 2006aj. All emission lines have similar width, and the profiles are symmetric, indicating that no major asymmetries are present in the ejecta at the velocities sampled by the nebular lines (v < 8000 km/s), except perhaps in the innermost part. The spectra were modelled with a non-LTE code. The mass of 56Ni required to power the emission spectrum is ~ 0.20 Msun, in excellent agreement with the results of early light curve modelling. The oxygen mass is ~ 1.5 Msun, again much less than in SN 1998bw but larger by ~ 0.7 Msun than the value derived from the early-time modelling. The total ejected mass is ~ 2 Msun below 8000 km/s. This confirms that SN 2006aj was only slightly more massive and energetic than the prototypical Type Ic SN 1994I, but also indicates the presence of a dense inner core, containing ~ 1 Msun of mostly oxygen and carbon. The presence of such a core is inferred for all broad-lined SNe Ic. This core may have the form of an equatorial oxygen-dominated region, but it is too deep to affect the early light curve and too small to affect the late polarization spectrum.Comment: 20 pages, 6 figures. Accepted for publication in the Astrophysical Journa

Blockade of constitutively activated ERK signaling enhances cytotoxicity of microtubule-destabilizing agents in tumor cells.

The extracellular signal-regulated kinase (ERK) signaling pathway is constitutively activated in many human tumor cell types. Given the cytoprotective role of this pathway, we examined whether its specific blockade might sensitize human tumor cells to the induction of apoptosis by various anticancer drugs. Although blockade of ERK signaling alone did not induce substantial cell death, it resulted in marked and selective enhancement of the induction of apoptosis by microtubule-destabilizing agents in tumor cells in which the ERK pathway is constitutively activated. The synergistic activation of c-Jun NH(2)-terminal kinase by the combination of an ERK pathway inhibitor and a microtubule-destabilizing agent appeared to be responsible, at least in part, for this effect. These results suggest that administration of the combination of an ERK pathway inhibitor and a microtubule-destabilizing agent is a potential chemotherapeutic strategy for the treatment of tumor cells with constitutive activation of the ERK pathway

Conditional deletion of Npt2b in phosphate transport

Background Hyperphosphatemia is common in chronic kidney disease and is associated with morbidity and mortality. The intestinal Na+-dependent phosphate transporter Npt2b is thought to be an important molecular target for the prevention of hyperphosphatemia. The role of Npt2b in the net absorption of inorganic phosphate (Pi), however, is controversial. Methods In the present study, we made tamoxifen-inducible Npt2b conditional knockout (CKO) mice to analyze systemic Pi metabolism, including intestinal Pi absorption. Results Although the Na+-dependent Pi transport in brush-border membrane vesicle uptake levels were significantly decreased in the distal intestine of Npt2b CKO mice compared with control mice, plasma Pi and fecal Pi excretion levels were not significantly different. Data obtained using the intestinal loop technique showed that Pi uptake in Npt2b CKO mice was not affected at a Pi concentration of 4 mM, which is considered the typical luminal Pi concentration after meals in mice. Claudin, which may be involved in paracellular pathways, as well as claudin-2, 12, and 15 protein levels were significantly decreased in the Npt2b CKO mice. Thus, Npt2b deficiency did not affect Pi absorption within the range of Pi concentrations that normally occurs after meals. Conclusion These findings indicate that abnormal Pi metabolism may also be involved in tight junction molecules such as Cldns that are affected by Npt2b deficiency

A Novel RNA-Recognition-Motif Protein Is Required for Premeiotic G1/S-Phase Transition in Rice (Oryza sativa L.)

The molecular mechanism for meiotic entry remains largely elusive in flowering plants. Only Arabidopsis SWI1/DYAD and maize AM1, both of which are the coiled-coil protein, are known to be required for the initiation of plant meiosis. The mechanism underlying the synchrony of male meiosis, characteristic to flowering plants, has also been unclear in the plant kingdom. In other eukaryotes, RNA-recognition-motif (RRM) proteins are known to play essential roles in germ-cell development and meiosis progression. Rice MEL2 protein discovered in this study shows partial similarity with human proline-rich RRM protein, deleted in Azoospermia-Associated Protein1 (DAZAP1), though MEL2 also possesses ankyrin repeats and a RING finger motif. Expression analyses of several cell-cycle markers revealed that, in mel2 mutant anthers, most germ cells failed to enter premeiotic S-phase and meiosis, and a part escaped from the defect and underwent meiosis with a significant delay or continued mitotic cycles. Immunofluorescent detection revealed that T7 peptide-tagged MEL2 localized at cytoplasmic perinuclear region of germ cells during premeiotic interphase in transgenic rice plants. This study is the first report of the plant RRM protein, which is required for regulating the premeiotic G1/S-phase transition of male and female germ cells and also establishing synchrony of male meiosis. This study will contribute to elucidation of similarities and diversities in reproduction system between plants and other species