A Rare Loss-of-Function Variant in Scavenger Receptor Class B Type I (SCARB1) Raises HDL Cholesterol and Increases Risk of Coronary Disease

Scavenger receptor BI (SR-BI) is the major receptor for high-density lipoprotein (HDL)<br/>cholesterol (HDL-C). In humans, high amounts of HDL-C in plasma are associated with a<br/>lower risk of coronary heart disease (CHD). Mice that have depleted Scarb1 (SR-BI<br/>knockout mice) have markedly elevated HDL-C levels but, paradoxically, increased<br/>atherosclerosis. The impact of SR-BI on HDL metabolism and CHD risk in humans remains<br/>unclear. Through targeted sequencing of coding regions of lipid-modifying genes in 328<br/>individuals with extremely high plasma HDL-C levels, we identified a homozygote for a lossof-function<br/>variant, in which leucine replaces proline 376 (P376L), in SCARB1, the gene<br/>encoding SR-BI. The P376L variant impairs posttranslational processing of SR-BI and<br/>abrogates selective HDL cholesterol uptake in transfected cells, in hepatocyte-like cells<br/>derived from induced pluripotent stem cells from the homozygous subject, and in mice.<br/>Large population-based studies revealed that subjects who are heterozygous carriers of<br/>the P376L variant have significantly increased levels of plasma HDL-C. P376L carriers have<br/>a profound HDL-related phenotype and an increased risk of CHD (odds ratio = 1.79, which is<br/>statistically significant).

Series-L/parallel-tuned Class-E power amplifier analysis

An analysis of the operation of a new series-L/parallel-tuned Class-E amplifier and its equivalence to the classic shunt-C/series-tuned Class-E amplifier are presented. The first reported closed form design equations for the series-L/parallel-tuned topology operating under ideal switching conditions are given, including the switch current and voltage in steady state, the circuit component values, the peak values of switch current and voltage and the power-output capability. Theoretical analysis is confirmed by numerical simulation for a 500 mW (27 dBm), 10% bandwidth, 5 V series-L/parallel-tuned, then, shunt-C/series-tuned Class-E power amplifier, operating at 2.5 GHz. Excellent agreement between theory and simulation results is achieved.

The VLT-FLAMES Tarantula Survey:V. the peculiar B[e]-like supergiant, VFTS698, in 30 Doradus

Aims. We present an analysis of a peculiar supergiant B-type star (VFTS698/Melnick 2/Parker 1797) in the 30 Doradus region of the Large Magellanic Cloud which exhibits characteristics similar to the broad class of B[e] stars. Methods. We analyse optical spectra from the VLT-FLAMES survey, together with archival optical and infrared photometry and X-ray imaging to characterise the system. Results. We find radial velocity variations of around 400 km s ^-1 in the high excitation Si iv, N iii and He ii spectra, and photometric variability of ∼0.6 mag with a period of 12.7 d. In addition, we detect long-term photometric variations of ∼0.25 mag, which may be due to a longer-term variability with a period of ∼400 d. Conclusions. We conclude that VFTS698 is likely an interacting binary comprising an early B-type star secondary orbiting a veiled, more massive companion. Spectral evidence suggests a mid-to-late B-type primary, but this may originate from an optically-thick accretion disc directly surrounding the primary. © 2012 ESO.

Characterization of IGH locus breakpoints in multiple myeloma indicates a subset of translocations appear to occur in pregerminal center B cells.

Translocations in myeloma are thought to occur solely in mature B cells in the germinal center through class switch recombination (CSR). We used a targeted captured technique followed by massively parallel sequencing to determine the exact breakpoints in both the immunoglobulin heavy chain (IGH) locus and the partner chromosome in 61 presentation multiple myeloma samples. The majority of samples (62%) have a breakpoint within the switch regions upstream of the IGH constant genes and are generated through CSR in a mature B cell. However, the proportion of CSR translocations is not consistent between cytogenetic subgroups. We find that 100% of t(4;14) are CSR-mediated; however, 21% of t(11;14) and 25% of t(14;20) are generated through DH-JH recombination activation gene-mediated mechanisms, indicating they occur earlier in B-cell development at the pro-B-cell stage in the bone marrow. These 2 groups also generate translocations through receptor revision, as determined by the breakpoints and mutation status of the segments used in 10% and 50% of t(11;14) and t(14;20) samples, respectively. The study indicates that in a significant number of cases the translocation-based etiological events underlying myeloma may arise at the pro-B-cell hematological progenitor cell level, much earlier in B-cell development than was previously thought.