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Status |
Public on Jan 28, 2024 |
Title |
Identification of PRMT1 as a suppressor of MHC-I and anti-tumour immunity |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
To understand the mechanisms by which Prmt1 knockout or inhibition sensitizes B16F10 to T cell mediated killing.
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Overall design |
B16F10 cells were pre-treated with Prmt1-inhibitor GSK3368715 (2.5 µM) for 2 days. Afterwards, untreated wildtype (controls), Prmt1-inhibitor treated or Prmt1-/- B16F10 were cultured for one more day in the presence or absence of mouse IFNγ (1 ng/ml). There are three independent replicates for each condition. Total RNA was then extracted, quantitated with 4200 Tapestation and finally, 1 µg of total RNA per sample was subjected to NGS library preparation (TruSeq RNA). NGS libraries were pooled and sequenced using a P2 100-cycle Illumina sequencing kit on the NextSeq 2000 sequencing system with paired-end 66bp reads.
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Contributor(s) |
Djajawi TM, Neil L, Pal B, Liao Y, Shi W, Kearney CJ |
Citation(s) |
38401121 |
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Submission date |
Sep 12, 2023 |
Last update date |
Apr 28, 2024 |
Contact name |
Wei Shi |
E-mail(s) |
Wei.Shi@onjcri.org.au
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Organization name |
Olivia Newton John Cancer Research Institute
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Department |
Bioinformatics and Cancer Genomics
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Street address |
Level 5, ONJ Cancer Centre, 145 Studley Rd
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City |
Heidelberg |
State/province |
VIC |
ZIP/Postal code |
3084 |
Country |
Australia |
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Platforms (1) |
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Samples (18)
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Relations |
BioProject |
PRJNA1016038 |