29 research outputs found

    First cohomology for finite groups of Lie type: simple modules with small dominant weights

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    Let kk be an algebraically closed field of characteristic p>0p > 0, and let GG be a simple, simply connected algebraic group defined over Fp\mathbb{F}_p. Given r≥1r \geq 1, set q=prq=p^r, and let G(Fq)G(\mathbb{F}_q) be the corresponding finite Chevalley group. In this paper we investigate the structure of the first cohomology group H1(G(Fq),L(λ))H^1(G(\mathbb{F}_q),L(\lambda)) where L(λ)L(\lambda) is the simple GG-module of highest weight λ\lambda. Under certain very mild conditions on pp and qq, we are able to completely describe the first cohomology group when λ\lambda is less than or equal to a fundamental dominant weight. In particular, in the cases we consider, we show that the first cohomology group has dimension at most one. Our calculations significantly extend, and provide new proofs for, earlier results of Cline, Parshall, Scott, and Jones, who considered the special case when λ\lambda is a minimal nonzero dominant weight.Comment: 24 pages, 5 figures, 6 tables. Typos corrected and some proofs streamlined over previous versio

    Second cohomology for finite groups of Lie type

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    Let GG be a simple, simply-connected algebraic group defined over Fp\mathbb{F}_p. Given a power q=prq = p^r of pp, let G(Fq)⊂GG(\mathbb{F}_q) \subset G be the subgroup of Fq\mathbb{F}_q-rational points. Let L(λ)L(\lambda) be the simple rational GG-module of highest weight λ\lambda. In this paper we establish sufficient criteria for the restriction map in second cohomology H2(G,L(λ))→H2(G(Fq),L(λ))H^2(G,L(\lambda)) \rightarrow H^2(G(\mathbb{F}_q),L(\lambda)) to be an isomorphism. In particular, the restriction map is an isomorphism under very mild conditions on pp and qq provided λ\lambda is less than or equal to a fundamental dominant weight. Even when the restriction map is not an isomorphism, we are often able to describe H2(G(Fq),L(λ))H^2(G(\mathbb{F}_q),L(\lambda)) in terms of rational cohomology for GG. We apply our techniques to compute H2(G(Fq),L(λ))H^2(G(\mathbb{F}_q),L(\lambda)) in a wide range of cases, and obtain new examples of nonzero second cohomology for finite groups of Lie type.Comment: 29 pages, GAP code included as an ancillary file. Rewritten to include the adjoint representation in types An, B2, and Cn. Corrections made to Theorem 3.1.3 and subsequent dependent results in Sections 3-4. Additional minor corrections and improvements also implemente

    Quantitative Proteomics Identify Novel miR-155 Target Proteins

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    Background: MicroRNAs are 22 nucleotides long non-coding RNAs and exert their function either by transcriptional or translational inhibition. Although many microRNA profiles in different tissues and disease states have already been discovered, only little is known about their target proteins. The microRNA miR-155 is deregulated in many diseases, including cancer, where it might function as an oncoMir. Methodology/Principal Findings: We employed a proteomics technique called ‘‘stable isotope labelling by amino acids in cell culture’ ’ (SILAC) allowing relative quantification to reliably identify target proteins of miR-155. Using SILAC, we identified 46 putative miR-155 target proteins, some of which were previously reported. With luciferase reporter assays, CKAP5 was confirmed as a new target of miR-155. Functional annotation of miR-155 target proteins pointed to a role in cell cycle regulation. Conclusions/Significance: To the best of our knowledge we have investigated for the first time miR-155 target proteins in the HEK293T cell line in large scale. In addition, by comparing our results to previously identified miR-155 target proteins i

    The Thermal State of the Accreting White Dwarf in AM Canum Venaticorum Binaries

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    Contains fulltext : 35202_1.pdf (preprint version ) (Open Access) Contains fulltext : 35202._2.pdf (publisher's version ) (Open Access)We calculate the heating and cooling of the accreting white dwarf (WD) in the ultracompact AM Canum Venaticorum (AM CVn) binaries and show that the WD can contribute significantly to their optical and ultraviolet emission. We estimate the WD's effective temperature, Teff, using the optical continuum for a number of observed binaries, and we show that it agrees well with our theoretical calculations. Driven by gravitational radiation losses, the time-averaged accretion rate, , decreases monotonically with increasing Porb, covering 6 orders of magnitude. If the short-period (Porbeff>50,000 K accreting WD. At longer Porb we calculate the Teff and absolute visual magnitude, MV, that the accreting WD will have during low accretion states, and we find that th

    Translocation (8;21) acute myeloid leukemia presenting as severe aplastic anemia

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    We report a case of t(8;21) acute myeloid leukemia presenting as severe aplastic anemia. While initial bone marrow biopsy lacked any cytogenetic abnormalities in 20 analyzed metaphases, repeat bone marrow biopsy eight days later demonstrated this translocation. Initial cytogenetic analysis of 20 metaphases was therefore insufficient to make the diagnosis of hypocellular acute myeloid leukemia. We discuss that further complementary molecular tests, such as CGH, would likely provide a more robust diagnosis of hematopoietic diseases

    Biofilm Formation and Detachment in Gram-Negative Pathogens Is Modulated by Select Bile Acids.

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    Biofilms are a ubiquitous feature of microbial community structure in both natural and host environments; they enhance transmission and infectivity of pathogens and provide protection from human defense mechanisms and antibiotics. However, few natural products are known that impact biofilm formation or persistence for either environmental or pathogenic bacteria. Using the combination of a novel natural products library from the fish microbiome and an image-based screen for biofilm inhibition, we describe the identification of taurine-conjugated bile acids as inhibitors of biofilm formation against both Vibrio cholerae and Pseudomonas aeruginosa. Taurocholic acid (1) was isolated from the fermentation broth of the fish microbiome-derived strain of Rhodococcus erythropolis and identified using standard NMR and MS methods. Screening of the twelve predominant human steroidal bile acid components revealed that a subset of these compounds can inhibit biofilm formation, induce detachment of preformed biofilms under static conditions, and that these compounds display distinct structure-activity relationships against V. cholerae and P. aeruginosa. Our findings highlight the significance of distinct bile acid components in the regulation of biofilm formation and dispersion in two different clinically relevant bacterial pathogens, and suggest that the bile acids, which are endogenous mammalian metabolites used to solubilize dietary fats, may also play a role in maintaining host health against bacterial infection
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