A Comprehensive Human cDNA Library For Functional Gene Replacement in Drosophila

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 3R24OD022005-05S1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2016
    2024
  • Known Financial Commitments (USD)

    $750,329
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    Hugo J Bellen
  • Research Location

    United States of America
  • Lead Research Institution

    Baylor College Of Medicine
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Pathogen morphology, shedding & natural history

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

PROJECT Summary: The recent pandemic of COVID-19 due to infection with the SARS-CoV-2 coronavirus has created an urgentneed to understand the biological mechanisms of pathogenesis of this new disease. The SARS-CoV-2 is acoronavirus with a slightly less than 30 kilobases (kb) long RNA genome that encodes 26 proteins that interactwith several hundred human proteins and initiate a number of pathogenic steps. Here we use the geneticmodel Drosophila melanogaster to understand gene and protein function involved in COVID-19. We willgenerate a library of UAS-cDNA constructs and transgenic flies to express and functionally assess the viralproteins. We will also generate transgenic flies for over 300 genes in the human genome involved in viralreplication and COVID-19 disease. We will generate Drosophila reagents for the Drosophila homologs of thesehuman genes using a unique drop-in technology and we will update the online hub for the dissemination ofthese resources to Drosophila labs throughout the world.