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-19Start & end year
20162024Known Financial Commitments (USD)
$750,329Funder
National Institutes of Health (NIH)Principal Investigator
Hugo J BellenResearch Location
United States of AmericaLead Research Institution
Baylor College Of MedicineResearch 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.