Dark Matters in Axino Gravitino Cosmology

It is suggested that the axino mass in the 1 MeV region and gravitino mass in the eV region can provide an axino lifetime of order of the time of photon decoupling. In this case, some undecayed axinos act like cold dark matters and some axino decay products (gravitinos and hot axions) act like hot dark matters at the time of galaxy formation.Comment: 9 pages, Late

Baryogenesis and Degenerate Neutrinos

We bring the theoretical issue of whether two important cosmological demands, baryon asymmetry and degenerate neutrinos as hot dark matter, can be compatible in the context of the seesaw mechanism. To realize leptogenesis with almost degenerate Majorana neutrinos without severe fine-tuning of parameters, we propose the hybrid seesaw mechanism with a heavy Higgs triplet and right-handed neutrinos. Constructing a minimal hybrid seesaw model with SO(3) flavor symmetry for the neutrino sector, we show that the mass splittings for the atmospheric and solar neutrino oscillations which are consistent with the requirements for leptogenesis can naturally arise.Comment: 13 pages with one figure using axodraw.st

Mammalian Ste20-Like Kinase and SAV1 Promote 3T3-L1 Adipocyte Differentiation by Activation of PPARγ

The mammalian ste20 kinase (MST) signaling pathway plays an important role in the regulation of apoptosis and cell cycle control. We sought to understand the role of MST2 kinase and Salvador homolog 1 (SAV1), a scaffolding protein that functions in the MST pathway, in adipocyte differentiation. MST2 and MST1 stimulated the binding of SAV1 to peroxisome proliferator-activated receptor γ (PPARγ), a transcription factor that plays a key role in adipogenesis. The interaction of endogenous SAV1 and PPARγ was detected in differentiating 3T3-L1 adipocytes. This binding required the kinase activity of MST2 and was mediated by the WW domains of SAV1 and the PPYY motif of PPARγ. Overexpression of MST2 and SAV1 increased PPARγ levels by stabilizing the protein, and the knockdown of SAV1 resulted in a decrease of endogenous PPARγ protein in 3T3-L1 adipocytes. During the differentiation of 3T3-L1 cells into adipocytes, MST2 and SAV1 expression began to increase at 2 days when PPARγ expression also begins to increase. MST2 and SAV1 significantly increased PPARγ transactivation, and SAV1 was shown to be required for the activation of PPARγ by rosiglitazone. Finally, differentiation of 3T3-L1 cells was augmented by MST2 and SAV1 expression and inhibited by knockdown of MST1/2 or SAV1. These results suggest that PPARγ activation by the MST signaling pathway may be a novel regulatory mechanism of adipogenesis

Targeted Inactivation of p12Cdk2ap1, CDK2 Associating Protein 1, Leads to Early Embryonic Lethality

Targeted disruption of murine Cdk2ap1, an inhibitor of CDK2 function and hence G1/S transition, results in the embryonic lethality with a high penetration rate. Detailed timed pregnancy analysis of embryos showed that the lethality occurred between embryonic day 3.5 pc and 5.5 pc, a period of implantation and early development of implanted embryos. Two homozygous knockout mice that survived to term showed identical craniofacial defect, including a short snout and a round forehead. Examination of craniofacial morphology by measuring Snout Length (SL) vs. Face Width (FW) showed that the Cdk2ap1+/− mice were born with a reduced SL/FW ratio compared to the Cdk2ap1+/+ and the reduction was more pronounced in Cdk2ap1−/− mice. A transgenic rescue of the lethality was attempted by crossing Cdk2ap1+/− animals with K14-Cdk2ap1 transgenic mice. Resulting Cdk2ap1+/−:K14-Cdk2ap1 transgenic mice showed an improved incidence of full term animals (16.7% from 0.5%) on a Cdk2ap1−/− background. Transgenic expression of Cdk2ap1 in Cdk2ap1−/−:K14-Cdk2ap1 animals restored SL/FW ratio to the level of Cdk2ap1+/−:K14-Cdk2ap1 mice, but not to that of the Cdk2ap1+/+:K14-Cdk2ap1 mice. Teratoma formation analysis using mESCs showed an abrogated in vivo pluripotency of Cdk2ap1−/− mESCs towards a restricted mesoderm lineage specification. This study demonstrates that Cdk2ap1 plays an essential role in the early stage of embryogenesis and has a potential role during craniofacial morphogenesis

Flaxino dark matter and stau decay

If the spontaneous breaking of Peccei-Quinn symmetry comes from soft supersymmetry breaking, the fermionic partners of the symmetry-breaking fields have mass of order the gravitino mass, and are called flatinos. The lightest flatino, called here the flaxino, is a CDM candidate if it is the lightest supersymmetric particle. We here explore flaxino dark matter assuming that the lightest ordinary supersymmetric particle is the stau, with gravity-mediated supersymmetry breaking. The decay of the stau to the flaxino is fast enough not to spoil the standard predictions of Big Bang Nucleosynthesis, and its track and decay can be seen in future colliders.Comment: 9 pages, 4 figures, to appear in JHE

Quasi Goldstone Fermion As a Sterile Neutrino

The existence of sterile neutrino is hinted by simultaneous explanation of diverse neutrino anomalies. We suggest that the quasi Goldstone fermions (QGF) arising in supersymmetric theory as a result of spontaneous breaking of global symmetry like the Peccei-Quinn symmetry or the lepton number symmetry can play a role of the sterile neutrino. The smallness of mass of QGF ($m_S \sim 10^{-3}-10$ eV) can be related to the specific choice of superpotential or K\"ahler potential (e.g., no-scale kinetic terms for certain superfields). Mixing of QGF with neutrinos implies the $R$-parity violation. It can proceed via the coupling of QGF with the Higgs supermultiplets or directly with the lepton doublet. A model which accounts for the solar and atmospheric anomalies and the dark matter is presented.Comment: 16 pages plus 3 figures include

The bone morphogenetic protein antagonist gremlin 1 is overexpressed in human cancers and interacts with YWHAH protein

BACKGROUND: Basic studies of oncogenesis have demonstrated that either the elevated production of particular oncogene proteins or the occurrence of qualitative abnormalities in oncogenes can contribute to neoplastic cellular transformation. The purpose of our study was to identify an unique gene that shows cancer-associated expression, and characterizes its function related to human carcinogenesis. METHODS: We used the differential display (DD) RT-PCR method using normal cervical, cervical cancer, metastatic cervical tissues, and cervical cancer cell lines to identify genes overexpressed in cervical cancers and identified gremlin 1 which was overexpressed in cervical cancers. We determined expression levels of gremlin 1 using Northern blot analysis and immunohistochemical study in various types of human normal and cancer tissues. To understand the tumorigenesis pathway of identified gremlin 1 protein, we performed a yeast two-hybrid screen, GST pull down assay, and immunoprecipitation to identify gremlin 1 interacting proteins. RESULTS: DDRT-PCR analysis revealed that gremlin 1 was overexpressed in uterine cervical cancer. We also identified a human gremlin 1 that was overexpressed in various human tumors including carcinomas of the lung, ovary, kidney, breast, colon, pancreas, and sarcoma. PIG-2-transfected HEK 293 cells exhibited growth stimulation and increased telomerase activity. Gremlin 1 interacted with homo sapiens tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, eta polypeptide (14-3-3 eta; YWHAH). YWHAH protein binding site for gremlin 1 was located between residues 61–80 and gremlin 1 binding site for YWHAH was found to be located between residues 1 to 67. CONCLUSION: Gremlin 1 may play an oncogenic role especially in carcinomas of the uterine cervix, lung, ovary, kidney, breast, colon, pancreas, and sarcoma. Over-expressed gremlin 1 functions by interaction with YWHAH. Therefore, Gremlin 1 and its binding protein YWHAH could be good targets for developing diagnostic and therapeutic strategies against human cancers

Peccei-Quinn NMSSM in the light of 125 GeV Higgs

We study the phenomenology of the Peccei-Quinn invariant extension of the next-to-minimal supersymmetric standard model (NMSSM) in view of the recent discovery of a 125 GeV Higgs boson. The minimal model having no quadratic and cubic terms of the NMSSM singlet field predicts a light singlino-like lightest supersymmetric particle (LSP). The model is strongly constrained by the Higgs invisible decay and the dark matter characteristic of the LSP, while some constraints can be relaxed by assuming that the saxion, the CP-even companion of the axion in the Peccei-Quinn sector, causes a late-time entropy production diluting the thermal LSP density. The collider signal of the model contains multi-jet and $h/W/Z$ plus missing energy, which can be discovered in the early stage of the 14 TeV LHC running.Comment: 40 pages, 10 figures, 6 tables. v3: references added, several statements added and corrected, comments on the small tadpole soft term added in sec. 2.