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Status |
Public on Aug 04, 2021 |
Title |
Cellular transcriptomes of wild-type and ING3 knockout HT-29 cells |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
The goal of this study is to use RNA-sequencing to profile the transcriptional changes in HT-29 cells with ING3 deficiency. Specifically, we were interested in determining the IFN and ISGs in response to ING3 KO. Several ISGs including IFI44L and IFITM1 were up-regulated in ING3 KO HT-29 cells, indicating that the broad resistance to virus infection in ING3 KO cells were mediated by heightened IFN and ISG responses.
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Overall design |
mRNA profiles of WT and ING3 KO HT-29 cells were analyzed by bulk RNA-sequencing We used one sgRNA to knockout ING3 in HT-29 cells, then we subcloned the HT-29-ING3 KO cells. #1 and #2 mean different subclones of HT-29-ING3 KO cells.
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Contributor(s) |
Song Y, Ding S |
Citation missing |
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Submission date |
Feb 04, 2021 |
Last update date |
Aug 04, 2021 |
Contact name |
Gaopeng Hou |
E-mail(s) |
[email protected]
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Phone |
3149065080
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Organization name |
Washinton University inSt. Louis
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Department |
molecular microbiology
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Street address |
McDonnell Pediatric Research Building, Rm 9220
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City |
St. Louis |
State/province |
MO |
ZIP/Postal code |
63110 |
Country |
USA |
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Platforms (1) |
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Samples (6)
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Relations |
BioProject |
PRJNA699603 |
SRA |
SRP304782 |