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Status |
Public on Dec 08, 2023 |
Title |
USP2 inhibition prevents infection with ACE2- dependent coronaviruses in vitro and is protective against SARS-CoV-2 in mice |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
In this study, we identified USP2 as a physiological deubiquitinase of ACE2 and USP2 inhibition led to ACE2 protein destruction, thereby preventing infections of coronaviruses that reliant on ACE2
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Overall design |
RNA-seq study of lung samples derived from K18-hACE2 mice infected with SARS-CoV-2 (Wuhan strain) and subjected to the treatment of vehicle control or USP2 inhibitor ML364
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Contributor(s) |
Dang F, Bai L, Lan K, Wei W |
Citation(s) |
38055802 |
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Submission date |
Jul 19, 2023 |
Last update date |
Dec 08, 2023 |
Contact name |
Fabin Dang |
E-mail(s) |
fdang@bidmc.harvard.edu
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Organization name |
Beth Israel Deaconess Medical Center
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Street address |
3 Blackfan Circle
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City |
Boston |
ZIP/Postal code |
02215 |
Country |
USA |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (12)
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Relations |
BioProject |
PRJNA996524 |
Supplementary file |
Size |
Download |
File type/resource |
GSE237741_Raw_Gene_Expression.csv.gz |
4.8 Mb |
(ftp)(http) |
CSV |
GSE237741_Vehicle_vs_ML364.DESeq.csv.gz |
3.6 Mb |
(ftp)(http) |
CSV |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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