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Status |
Public on Nov 04, 2009 |
Title |
Wild type vs. Nova2 KO mouse: Exon array data |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
To assess the requirement of Nova2 for alternative processing of RNA in mouse brain. Protein-RNA interactions play critical roles in all aspects of gene expression. Here we develop a genome-wide means of mapping protein-RNA binding sites in vivo, by high throughput sequencing of RNA isolated by crosslinking immunoprecipitation (HITS-CLIP). HITS-CLIP analysis of the neuron-specific splicing factor Nova2 revealed extremely reproducible RNA binding maps in multiple mouse brains. These maps provide genome-wide in vivo biochemical footprints confirming the previous prediction that the position of Nova binding determines the outcome of alternative splicing; moreover, they are sufficiently powerful to predict Nova action de novo. HITS-CLIP revealed a large number of Nova-RNA interactions in 3’ UTRs, leading to the discovery that Nova regulates alternative polyadenylation in the brain. HITS-CLIP, therefore, provides a robust, unbiased means to identify functional protein-RNA interactions in vivo.
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Overall design |
RNA from the cortex of 4 wild type and 4 Nova2 KO P10 CD1 mice. One array per biological replicate.
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Contributor(s) |
Licatalosi DD, Darnell RB |
Citation(s) |
18978773 |
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Submission date |
Jul 28, 2009 |
Last update date |
Mar 03, 2017 |
Contact name |
Donny D Licatalosi |
Organization name |
Case Western Reserve University
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Lab |
Licatalosi
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Street address |
10900 Euclid Ave
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City |
Cleveland |
State/province |
OH |
ZIP/Postal code |
44106 |
Country |
USA |
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Platforms (1) |
GPL6193 |
[MoEx-1_0-st] Affymetrix Mouse Exon 1.0 ST Array [probe set (exon) version] |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE12965 |
Wild type vs. Nova2 KO mouse P10 cortex RNA |
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Relations |
BioProject |
PRJNA119105 |