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Status |
Public on Mar 30, 2016 |
Title |
In vivo analysis of astrocyte ribosome-associated mRNA after traumatic spinal cord injury |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Analysis of gene expression by astrocytes or non-astrocyte cells in spinal cord injury (SCI) lesions may lead to the identification of molecules that impact on axon regrowth. We conducted genome-wide RNA sequencing of (i) immunoprecipitated astrocyte-specific ribosome-associated RNA (ramRNA) from WT or STAT3-CKO astrocytes, and (ii) the non-precipitated (flow-through) RNA deriving from non-astrocyte cells in the same tissue samples 14 days following SCI. DOI: 10.1038/nature17623
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Overall design |
Young adult female mGFAP-Cre-RiboTag or mGFAP-Cre-RiboTag-STAT3-LoxP mice underwent severe crush SCI at thoracic level 10. 14 days following SCI, the central 3mm of the SCI lesion was extracted, homogenized and (i) astrocyte-specific ribosome-associated RNA (ramRNA) precipitated via a hemagglutinin (HA) tag targeted to either WT (n=4) or STAT3-CKO (n=3) astrocytes, and (ii) the non-precipitated (flow-through) RNA deriving from non-astrocyte cells in the same tissue samples. Sex and age-matched mGFAP-Cre-RiboTag mice served as uninjured controls (n=4).
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Contributor(s) |
Burda JE, Anderson MA, Ren Y, O'Shea TM, Kawaguchi R, Coppola G, Khakh BS, Deming TJ, Sofroniew MV |
Citation(s) |
27027288 |
Submission date |
Dec 17, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Riki Kawaguchi |
E-mail(s) |
rkawaguchi@mednet.ucla.edu
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Phone |
4244424783
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Organization name |
University of California Los Angeles
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Department |
Department of Neurology and Department of Psychiatry
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Lab |
Informatics Center for Neurogenetics and Neurogenomics (ICNN).
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Street address |
760 Westwood Plaza, Room 37-420
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City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90095-1759 |
Country |
USA |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (22)
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Relations |
BioProject |
PRJNA306222 |
SRA |
SRP067494 |