61 research outputs found

    The Unconserved Groucho Central Region Is Essential for Viability and Modulates Target Gene Specificity

    Get PDF
    Groucho (Gro) is a Drosophila corepressor required by numerous DNA-binding repressors, many of which are distributed in gradients and provide positional information during development. Gro contains well-conserved domains at its N- and C-termini, and a poorly conserved central region that includes the GP, CcN, and SP domains. All lethal point mutations in gro map to the conserved regions, leading to speculation that the unconserved central domains are dispensable. However, our sequence analysis suggests that the central domains are disordered leading us to suspect that the lack of lethal mutations in this region reflects a lack of order rather than an absence of essential functions. In support of this conclusion, genomic rescue experiments with Gro deletion variants demonstrate that the GP and CcN domains are required for viability. Misexpression assays using these same deletion variants show that the SP domain prevents unrestrained and promiscuous repression by Gro, while the GP and CcN domains are indispensable for repression. Deletion of the GP domain leads to loss of nuclear import, while deletion of the CcN domain leads to complete loss of repression. Changes in Gro activity levels reset the threshold concentrations at which graded repressors silence target gene expression. We conclude that co-regulators such as Gro are not simply permissive components of the repression machinery, but cooperate with graded DNA-binding factors in setting borders of gene expression. We suspect that disorder in the Gro central domains may provide the flexibility that allows this region to mediate multiple interactions required for repression

    SPARC 2016 Salford postgraduate annual research conference book of abstracts

    Get PDF

    Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.

    Get PDF
    Clinical outcome upon infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ranges from silent infection to lethal coronavirus disease 2019 (COVID-19). We have found an enrichment in rare variants predicted to be loss-of-function (LOF) at the 13 human loci known to govern Toll-like receptor 3 (TLR3)- and interferon regulatory factor 7 (IRF7)-dependent type I interferon (IFN) immunity to influenza virus in 659 patients with life-threatening COVID-19 pneumonia relative to 534 subjects with asymptomatic or benign infection. By testing these and other rare variants at these 13 loci, we experimentally defined LOF variants underlying autosomal-recessive or autosomal-dominant deficiencies in 23 patients (3.5%) 17 to 77 years of age. We show that human fibroblasts with mutations affecting this circuit are vulnerable to SARS-CoV-2. Inborn errors of TLR3- and IRF7-dependent type I IFN immunity can underlie life-threatening COVID-19 pneumonia in patients with no prior severe infection

    Homeodomain proteins: an update

    Get PDF

    Effects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspring

    Get PDF

    On the Advancement of Maintenance Management Towards Smart Maintenance in Manufacturing

    No full text
    The purpose of this work is to envision the future of maintenance without forgetting the past and present of maintenance practices. Indeed, there is a big potential for maintenance, fostered by the promises of the Fourth Indus-trial Revolution. At the same time, there is still a widespread evidence of the state of practices leading to assert that maintenance is not yet advanced as it would be expected. Thus, comparing the vision supported by advanced maintenance systems, through the concepts of E-maintenance, Internet of Things and Cyber Physical Systems, with the evidences on the state of prac-tices collected based on a sample of more than 300 industrial plants, we come up with a reflection on the advancement of maintenance management towards Smart Maintenance
    corecore