Phosphorylation-dependent regulation of the RNA metabolism in the host response to coronavirus infection

Grant number: 197785619

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Key facts

  • Disease

    COVID-19
  • start year

    2013
  • Known Financial Commitments (USD)

    $0
  • Funder

    DFG
  • Principal Investigator

    Michael Kracht
  • Research Location

    Germany
  • Lead Research Institution

    Philipps-University Marburg and Justus-Liebig-University Giessen
  • Research Priority Alignment

    N/A
  • Research Category

    N/A

  • Research Subcategory

    N/A

  • Special Interest Tags

    N/A

  • Study Type

    Unspecified

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

Part of the Collaborative Research Centre CRC 1021 "RNA Viruses: RNA Metabolism, Host Response and Pathogenesis" at Philipps-Universität Marburg with Justus-Liebig-Universität Giessen, funded since 2013. The molecular mechanisms affecting individual steps of gene expression in coronavirus- infected cells are largely unknown. By exploiting a comprehensive set of transcriptome, ChIP-seq and proteomics data we will work out the functional relevance of the most strongly regulated (i) non-coding genomic regions, (ii) signaling proteins (transcription factors, mRNA decay factors, protein kinases) and (iii) protein modifications. This analysis will generate new mechanistic insight into the CoV-regulated signaling network that controls HCoV-229E replication or the expression of host cell gene

Publicationslinked via Europe PMC

Serosurveillance identifies an endemic hotspot of Lassa fever in Faranah, Upper Guinea.

MyosinVb tail inhibits transport of Marburg virus glycoprotein GP to VP40-enriched sites at the plasma membrane.

Long COVID: Pathophysiology, current concepts, and future directions.

Exclusion of Superinfection or Enhancement of Superinfection in Pestiviruses-APPV Infection Is Not Dependent on ADAM17.

Essential role of <i>cis</i>-encoded mature NS3 in the genome packaging of classical swine fever virus.

Nucleocapsids of the Rift Valley fever virus ambisense S segment contain an exposed RNA element in the center that overlaps with the intergenic region.

Effects of long-term corticosteroid use on susceptibility to respiratory viruses: a narrative review.

Urinary eosinophil-derived neurotoxin is associated with reduced lung function in pediatric asthma.

Impact of different tissue dissociation protocols on endothelial cell recovery from developing mouse lungs.