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

Binding of Glycyl-tRNA synthetase to Mengovirus RNA stimulates translation.

Serosurveillance Identifies an Endemic Hotspot of Lassa Fever in Faranah, Upper Guinea.

Interaction between W41 of the hepatitis B virus preS1 surface peptide and Y146/F274 of the cellular receptor molecule Na<sup>+</sup>/taurocholate co-transporting polypeptide is essential for virus entry.

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 cis-encoded mature NS3 in the genome packaging of classical swine fever virus.

Infections in immunocompromised hosts: progress made and challenges ahead.

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