Energy Efficient Transmission over Space Shift Keying Modulated MIMO Channels

Energy-efficient communication using a class of spatial modulation (SM) that encodes the source information entirely in the antenna indices is considered in this paper. The energy-efficient modulation design is formulated as a convex optimization problem, where minimum achievable average symbol power consumption is derived with rate, performance, and hardware constraints. The theoretical result bounds any modulation scheme of this class, and encompasses the existing space shift keying (SSK), generalized SSK (GSSK), and Hamming code-aided SSK (HSSK) schemes as special cases. The theoretical optimum is achieved by the proposed practical energy-efficient HSSK (EE-HSSK) scheme that incorporates a novel use of the Hamming code and Huffman code techniques in the alphabet and bit-mapping designs. Experimental studies demonstrate that EE-HSSK significantly outperforms existing schemes in achieving near-optimal energy efficiency. An analytical exposition of key properties of the existing GSSK (including SSK) modulation that motivates a fundamental consideration for the proposed energy-efficient modulation design is also provided

Changes in the abundance of blue-green algae related to nutrient loadings in the nearshore of Lake Michigan

Nutrient loadings to the nearshore of southeastern Lake Michigan have undergone a remarkable reduction. This reduction can affect the nutrient supply and result in biological changes. Changes in phytoplankton community, particularly the blue-green algae, can be related to nutrient changes. After thermal stratification, sudden increases in the blue-green algae population were significantly correlated to soluble reactive phosphorus concentrations. Phosphorus-stimulated low dissolved silica and phosphorus limitations after stratification appear to be primary factors contributing to the success of these algae.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/42875/1/10750_2004_Article_BF00004203.pd

A numerical simulation of trichromatic equations in chlorophyll estimation using the spectrophotometric technique

A numerical simulation of trichromatic pigment equations is made with the aid of a computer utility program. Significant quantitative differences in the estimates of pigment concentration result from using different sets of trichromatic equations. Estimates of chlorophylls a, b , and c were found highly correlated with the application of the equations, even though the absorbance values used as input for the stimulation are not correlated.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/42911/1/10750_2004_Article_BF00006323.pd

An In Vivo Screen Identifies PYGO2 as a Driver for Metastatic Prostate Cancer

Advanced prostate cancer displays conspicuous chromosomal instability and rampant copy number aberrations, yet the identity of functional drivers resident in many amplicons remain elusive. Here, we implemented a functional genomics approach to identify new oncogenes involved in prostate cancer progression. Through integrated analyses of focal amplicons in large prostate cancer genomic and transcriptomic datasets as well as genes upregulated in metastasis, 276 putative oncogenes were enlisted into an in vivo gain-of-function tumorigenesis screen. Among the top positive hits, we conducted an in-depth functional analysis on Pygopus family PHD finger 2 (PYGO2), located in the amplicon at 1q21.3. PYGO2 overexpression enhances primary tumor growth and local invasion to draining lymph nodes. Conversely, PYGO2 depletion inhibits prostate cancer cell invasion in vitro and progression of primary tumor and metastasis in vivo In clinical samples, PYGO2 upregulation associated with higher Gleason score and metastasis to lymph nodes and bone. Silencing PYGO2 expression in patient-derived xenograft models impairs tumor progression. Finally, PYGO2 is necessary to enhance the transcriptional activation in response to ligand-induced Wnt/β-catenin signaling. Together, our results indicate that PYGO2 functions as a driver oncogene in the 1q21.3 amplicon and may serve as a potential prognostic biomarker and therapeutic target for metastatic prostate cancer.Significance: Amplification/overexpression of PYGO2 may serve as a biomarker for prostate cancer progression and metastasis. Cancer Res; 78(14); 3823-33. ©2018 AACR

Opposing roles of TGFβ and BMP signaling in prostate cancer development

SMAD4 constrains progression of Pten-null prostate cancer and serves as a common downstream node of transforming growth factor β (TGFβ) and bone morphogenetic protein (BMP) pathways. Here, we dissected the roles of TGFβ receptor II (TGFBR2) and BMP receptor II (BMPR2) using a Pten-null prostate cancer model. These studies demonstrated that the molecular actions of TGFBR2 result in both SMAD4-dependent constraint of proliferation and SMAD4-independent activation of apoptosis. In contrast, BMPR2 deletion extended survival relative to Pten deletion alone, establishing its promoting role in BMP6-driven prostate cancer progression. These analyses reveal the complexity of TGFβ-BMP signaling and illuminate potential therapeutic targets for prostate cancer

Structural basis for the RING catalyzed synthesis of K63 linked ubiquitin chains

This work was supported by grants from Cancer Research UK (C434/A13067), the Wellcome Trust (098391/Z/12/Z) and Biotechnology and Biological Sciences Research Council (BB/J016004/1).The RING E3 ligase catalysed formation of lysine 63 linked ubiquitin chains by the Ube2V2–Ubc13 E2 complex is required for many important biological processes. Here we report the structure of the RING domain dimer of rat RNF4 in complex with a human Ubc13~Ub conjugate and Ube2V2. The structure has captured Ube2V2 bound to the acceptor (priming) ubiquitin with Lys63 in a position that could lead to attack on the linkage between the donor (second) ubiquitin and Ubc13 that is held in the active “folded back” conformation by the RING domain of RNF4. The interfaces identified in the structure were verified by in vitro ubiquitination assays of site directed mutants. This represents the first view of the synthesis of Lys63 linked ubiquitin chains in which both substrate ubiquitin and ubiquitin-loaded E2 are juxtaposed to allow E3 ligase mediated catalysis.PostprintPeer reviewe