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Status |
Public on Mar 01, 2023 |
Title |
HyperTRIBE uncovers SYNCRIP RNA binding activity in hematopoietic stem cells (HSCs) and multipotent progenitors (MPPs) |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing Other
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Summary |
Identifying SYNCRIP RNA-binding targets in HSC and MPP populations, in order to uncover which direct targets influence SYNCRIP's role in maintaining HSCs self renewal capacity.
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Overall design |
HSCs (Lin-, Sca1+, cKit+, CD150+ CD48-) and MPPs (Lin-, Sca1+, cKit+, all remaining CD150 CD48 cells) from C57BL/6 mice (The Jackson Laboratory, USA) were FACS sorted and transduced with virus expressing either empty vector (MSCV-IRES-GFP) or SYNCRIP-ADAR. 48hrs post transduction cells were sorted for GFP+ expression and used for RNA-seq.
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Contributor(s) |
Vu LP, Herrejon Chavez F, Chu KL, Kharas MG |
Citation(s) |
37085479 |
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Submission date |
May 08, 2022 |
Last update date |
May 12, 2023 |
Contact name |
Michael Kharas |
E-mail(s) |
kharasm@mskcc.org
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Organization name |
Mamorial Sloan Kettering Cancer Center
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Department |
Molecular Pharmacology Program
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Lab |
Michael Kharas
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Street address |
417 68th street
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City |
new york |
State/province |
New York |
ZIP/Postal code |
10065 |
Country |
USA |
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Platforms (1) |
GPL21103 |
Illumina HiSeq 4000 (Mus musculus) |
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Samples (12)
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Relations |
BioProject |
PRJNA836258 |