The far-ultraviolet signature of the 'missing' baryons in the Local Group of galaxies

The number of baryons detected in the low-redshift (z < 1) Universe is far smaller than the number detected in corresponding volumes at higher redshifts. Simulations of the formation of structure in the Universe show that up to two-thirds of the 'missing' baryons may have escaped detection because of their high temperature and low density. One of the few ways to detect this matter directly is to look for its signature in the form of ultraviolet absorption lines in the spectra of background sources such as quasars. Here we show that the amplitude of the average velocity vector of 'high velocity' O vi (O5+) absorption clouds detected in a survey of ultraviolet emission from active galactic nuclei decreases significantly when the vector is transformed to the frames of the Galactic Standard of Rest and the Local Group of galaxies. At least 82 per cent of these absorbers are not associated with any 'high velocity' atomic hydrogen complex in our Galaxy, and are therefore likely to result from a primordial warm-hot intergalactic medium pervading an extended corona around the Milky Way or the Local Group. The total mass of baryons in this medium is estimated to be up to approximately 10(12) solar masses, which is of the order of the mass required to dynamically stabilize the Local Group.     

Humanin peptide suppresses apoptosis by interfering with Bax activation

Bax (Bcl2-associated X protein) is an apoptosis-inducing protein that participates in cell death during normal development and in various diseases. Bax resides in an inactive state in the cytosol of many cells. In response to death stimuli, Bax protein undergoes conformational changes that expose membrane-targeting domains, resulting in its translocation to mitochondrial membranes, where Bax inserts and causes release of cytochrome c and other apoptogenic proteins. It is unknown what controls conversion of Bax from the inactive to active conformation. Here we show that Bax interacts with humanin (HN), an anti-apoptotic peptide of 24 amino acids encoded in mammalian genomes. HN prevents the translocation of Bax from cytosol to mitochondria. Conversely, reducing HN expression by small interfering RNAs sensitizes cells to Bax and increases Bax translocation to membranes. HN peptides also block Bax association with isolated mitochondria, and suppress cytochrome c release in vitro. Notably, the mitochondrial genome contains an identical open reading frame, and the mitochondrial version of HN can also bind and suppress Bax. We speculate therefore that HN arose from mitochondria and transferred to the nuclear genome, providing a mechanism for protecting these organelles from Bax.     

A first-generation linkage disequilibrium map of human chromosome 22

DNA sequence variants in specific genes or regions of the human genome are responsible for a variety of phenotypes such as disease risk or variable drug response. These variants can be investigated directly, or through their non-random associations with neighbouring markers (called linkage disequilibrium (LD)). Here we report measurement of LD along the complete sequence of human chromosome 22. Duplicate genotyping and analysis of 1,504 markers in Centre d'Etude du Polymorphisme Humain (CEPH) reference families at a median spacing of 15 kilobases (kb) reveals a highly variable pattern of LD along the chromosome, in which extensive regions of nearly complete LD up to 804 kb in length are interspersed with regions of little or no detectable LD. The LD patterns are replicated in a panel of unrelated UK Caucasians. There is a strong correlation between high LD and low recombination frequency in the extant genetic map, suggesting that historical and contemporary recombination rates are similar. This study demonstrates the feasibility of developing genome-wide maps of LD.     

Age of long sediment cores from Lake Baikal

The new BDP-98 drill core of the Baikal Drilling Project is a key palaeoclimate record in continental Asia because globally sensitive sedimentary records of such length and continuity are very rare. Kashiwaya et al. have attempted signal processing of the BDP-98 average grain-size record, but in constructing their age model they excised a 100-metre interval from the 600-metre section, stating that it is "erroneous". On the basis of our lithological studies, we consider that this excision is unjustified.     

Using Co-operative Inquiry with Black Women Managers: Exploring Possibilities for Moving from Surviving to Thriving

This paper recounts and explores the early stages of a Black women managers' Co-operative Inquiry group exploring strategies for moving from surviving to thriving. The term Black describes any person perceived not to be White. It considers why Action Research methodology was perceived to be appropriate for this work, outlines key considerations attended to in setting up the inquiry, and then, briefly, explores some of the dilemmas encountered and insights gained in the process of undertaking the inquiry. To ensure confidentiality all names used are fictional ones chosen by the individuals.     

Aryl hydrocarbon hydroxylase activity in type II alveolar lung cells

Summary Type II alveolar lung cells metabolize polycyclic aromatic hydrocarbons as indicated by measurements of aryl hydrocarbon hydroxylase activity and binding of tritium labeled benzo(a)pyrene to nuclear and cytoplasmic components.     

An evaluation of five algorithms for generating an initial configuration for SINDSCAL

Five different methods for obtaining a rational initial estimate of the stimulus space in the INDSCAL model were compared using the SINDSCAL program for fitting INDSCAL. The effect of the number of stimuli, the number of subjects, the dimensionality, and the amount of error on the quality and efficiency of the final SINDSCAL solution were investigated in a Monte Carlo study. We found that the quality of the final solution was not affected by the choice of the initialization method, suggesting that SINDSCAL finds a global optimum regardless of the initialization method used. The most efficient procedures were the methods proposed by by de Leeuw and Pruzansky (1978) and by Flury and Gautschi (1986) for the simultaneous diagonalization of several positive definite symmetric matrices, and a method based on linearly constraining the stimulus space using the CANDELINC approach developed by Carroll, Pruzansky, and Kruskal (1980).Geert De Soete is supported as Bevoegdverklaard Navorser of the Belgian Nationaal Fonds voor Wetenschappelijk Onderzoek. The authors gratefully acknowledge the helpful comments and suggestions of the reviewers.     

Variations in DNA elucidate molecular networks that cause disease

Identifying variations in DNA that increase susceptibility to disease is one of the primary aims of genetic studies using a forward genetics approach. However, identification of disease-susceptibility genes by means of such studies provides limited functional information on how genes lead to disease. In fact, in most cases there is an absence of functional information altogether, preventing a definitive identification of the susceptibility gene or genes. Here we develop an alternative to the classic forward genetics approach for dissecting complex disease traits where, instead of identifying susceptibility genes directly affected by variations in DNA, we identify gene networks that are perturbed by susceptibility loci and that in turn lead to disease. Application of this method to liver and adipose gene expression data generated from a segregating mouse population results in the identification of a macrophage-enriched network supported as having a causal relationship with disease traits associated with metabolic syndrome. Three genes in this network, lipoprotein lipase (Lpl), lactamase beta (Lactb) and protein phosphatase 1-like (Ppm1l), are validated as previously unknown obesity genes, strengthening the association between this network and metabolic disease traits. Our analysis provides direct experimental support that complex traits such as obesity are emergent properties of molecular networks that are modulated by complex genetic loci and environmental factors.