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The international monitoring system exists to verify compliance with the terms of the comprehensive test ban treaty. About 10% of the member stations will be capable of detecting radioxenon, which can be produced in nuclear detonations or through civilian processes. We have studied the activation of radioxenon by the prompt, intense spectrum of 14-MeV neutrons produced at the National Ignition Facility. While 14-MeV neutrons are not currently a significant contributor to the production of radioxenon, we find that radioxenon produced through activation of environmental xenon by 14-MeV neutrons would be distinguishable from activation by nuclear tests. [ABSTRACT FROM AUTHOR]

We determined fission yields of xenon (Xe, Xe, Xe, Xe, Xe, and Xe) resulting from 14 MeV neutron induced fission of depleted uranium at the National Ignition Facility. Measurements begin approximately 20 s after shot time, and yields have been determined for nuclides with half-lives as short as tens of seconds. We determined the relative independent yields of Xe, Xe, and Xe to significantly higher precision than previously reported. The relative fission yields of all nuclides are statistically indistinguishable from values reported by England and Rider (ENDF-349. LA-UR-94-3106, ), with exception of the cumulative yield of Xe. Considerable differences exist between our measured yields and the JEFF-3.1 database values. [ABSTRACT FROM AUTHOR]

The basic-region leucine zipper (BR-LZ or bZIP) transcription factors dimerize via their LZ domains to position the adjacent BRs for DNA binding. Members of the C/EBP, AP-1 and CREB/ATF bZIP subfamilies form homodimeric or heterodimeric complexes with other members of the same subset and bind-specific DNA motifs. Here we demonstrate that C/EBPα also zippers with AP-1 proteins and that this interaction allows contact with novel DNA elements and induction of monocyte lineage commitment in myeloid progenitors. A leucine zipper swap:gel shift assay demonstrates that C/EBPα zippers with c-Jun, JunB or c-Fos, but not with c-Maf or MafB. To evaluate activities of specific homodimers or heterodimers we utilized LZs with acid (LZE) or basic (LZK) residues in their salt bridge positions. C/EBPαLZE:C/EBPαLZK preferentially binds a C/EBP site, c-JunLZE:c-FosLZK an AP-1 site and C/EBPαLZE:c-JunLZK a hybrid element identified as TTGCGTCAT by oligonucleotide selection. In murine myeloid progenitors, C/EBPα:c-Jun or C/EBPα:c-Fos LZE:LZK heterodimers induce monocyte lineage commitment with markedly increased potency compared with C/EBPα or c-Jun homodimers or c-Jun:c-Fos heterodimers, demonstrating a positive functional consequence of C/EBP:AP-1 bZIP subfamily interaction. C/EBPα:cJun binds and activates the endogenous PU.1 promoter, providing one mechanism for induction of monopoiesis by this complex.Oncogene (2008) 27, 2772–2779; doi:10.1038/sj.onc.1210940; published online 19 November 2007 [ABSTRACT FROM AUTHOR]