CLIP Identifies Nova-Regulated RNA Networks in the Brain
Top Cited Papers
- 14 November 2003
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 302 (5648) , 1212-1215
- https://doi.org/10.1126/science.1090095
Abstract
Nova proteins are neuron-specific antigens targeted in paraneoplastic opsoclonus myoclonus ataxia (POMA), an autoimmune neurologic disease characterized by abnormal motor inhibition.Nova proteins regulate neuronal pre-messenger RNA splicing by directly binding to RNA.To identify Nova RNA targets, we developed a method to purify protein-RNA complexes from mouse brain with the use of ultraviolet cross-linking and immunoprecipitation (CLIP).Thirty-four transcripts were identified multiple times by Nova CLIP.Three-quarters of these encode proteins that function at the neuronal synapse, and one-third are involved in neuronal inhibition.Splicing targets confirmed in Nova–/– mice include c-Jun N-terminal kinase 2, neogenin, and gephyrin; the latter encodes a protein that clusters inhibitory γ-aminobutyric acid and glycine receptors, two previously identified Nova splicing targets.Thus, CLIP reveals that Nova coordinately regulates a biologically coherent set of RNAs encoding multiple components of the inhibitory synapse, an observation that may relate to the cause of abnormal motor inhibition in POMA.Keywords
This publication has 31 references indexed in Scilit:
- Nova Regulates GABAA Receptor γ2 Alternative Splicing via a Distal Downstream UCAU-Rich Intronic Splicing EnhancerMolecular and Cellular Biology, 2003
- Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X SyndromeCell, 2001
- Ion channels and epilepsyAmerican Journal of Medical Genetics, 2001
- The splice of life: Alternative splicing and neurological diseaseNature Reviews Neuroscience, 2001
- A brain-enriched polypyrimidine tract-binding protein antagonizes the ability of Nova to regulate neuron-specific alternative splicingProceedings of the National Academy of Sciences, 2000
- The tetranucleotide UCAY directs the specific recognition of RNA by the Nova K-homology 3 domainProceedings of the National Academy of Sciences, 2000
- Sequence-Specific RNA Binding by a Nova KH DomainCell, 2000
- Deleted in Colorectal Cancer (DCC) Encodes a Netrin ReceptorCell, 1996
- Identification of four splice variants of the mouse stress-activated protein kinase JNK/SAPK α-isoformNeuroReport, 1996
- Snurps and scyrpsCell, 1981