Submitted by ja607 on
|Title||Cell type-specific CLIP reveals that NOVA regulates cytoskeleton interactions in motoneurons.|
|Publication Type||Journal Article|
|Year of Publication||2018|
|Authors||Yuan, Y, Xie, S, Darnell, JC, Darnell, AJ, Saito, Y, Phatnani, H, Murphy, EA, Zhang, C, Maniatis, T, Darnell, RB|
|Date Published||2018 08 15|
|Keywords||Alternative Splicing, Amino Acid Sequence, Animals, Cercopithecus aethiops, Chromosomes, Artificial, Bacterial, COS Cells, Cross-Linking Reagents, Cytoskeleton, Dendrites, Exons, Immunoprecipitation, Lipoylation, Mice, Mice, Transgenic, Motor Neurons, Nerve Tissue Proteins, NIH 3T3 Cells, Pseudopodia, RNA, RNA-Binding Proteins, Septins, Transcriptome|
BACKGROUND: Alternative RNA processing plays an essential role in shaping cell identity and connectivity in the central nervous system. This is believed to involve differential regulation of RNA processing in various cell types. However, in vivo study of cell type-specific post-transcriptional regulation has been a challenge. Here, we describe a sensitive and stringent method combining genetics and CLIP (crosslinking and immunoprecipitation) to globally identify regulatory interactions between NOVA and RNA in the mouse spinal cord motoneurons.
RESULTS: We developed a means of undertaking motoneuron-specific CLIP to explore motoneuron-specific protein-RNA interactions relative to studies of the whole spinal cord in mouse. This allowed us to pinpoint differential RNA regulation specific to motoneurons, revealing a major role for NOVA in regulating cytoskeleton interactions in motoneurons. In particular, NOVA specifically promotes the palmitoylated isoform of the cytoskeleton protein Septin 8 in motoneurons, which enhances dendritic arborization.
CONCLUSIONS: Our study demonstrates that cell type-specific RNA regulation is important for fine tuning motoneuron physiology and highlights the value of defining RNA processing regulation at single cell type resolution.
|Alternate Journal||Genome Biol.|
|PubMed Central ID||PMC6092797|
|Grant List||R35 NS097404 / NS / NINDS NIH HHS / United States |
RC2 NS069473 / NS / NINDS NIH HHS / United States
UM1 HG008901 / HG / NHGRI NIH HHS / United States
5RC2NS069473-02 / NH / NIH HHS / United States