| Literature DB >> 30638744 |
Yuhki Saito1, Yuan Yuan2, Ilana Zucker-Scharff2, John J Fak2, Saša Jereb2, Yoko Tajima2, Donny D Licatalosi3, Robert B Darnell4.
Abstract
RNA-binding proteins (RBPs) regulate genetic diversity, but the degree to which they do so in individual cell types in vivo is unknown. We developed NOVA2 cTag-crosslinking and immunoprecipitation (CLIP) to generate functional RBP-RNA maps from different neuronal populations in the mouse brain. Combining cell type datasets from Nova2-cTag and Nova2 conditional knockout mice revealed differential NOVA2 regulatory actions on alternative splicing (AS) on the same transcripts expressed in different neurons. This includes functional differences in transcripts expressed in cortical and cerebellar excitatory versus inhibitory neurons, where we find NOVA2 is required for, respectively, development of laminar structure, motor coordination, and synapse formation. We also find that NOVA2-regulated AS is coupled to NOVA2 regulation of intron retention in hundreds of transcripts, which can sequester the trans-acting splicing factor PTBP2. In summary, cTag-CLIP complements single-cell RNA sequencing (RNA-seq) studies by providing a means for understanding RNA regulation of functional cell diversity.Entities:
Keywords: CLIP; NOVA2; PTBP2; RNA-binding protein; alternative splicing; cTag-CLIP; conditional knockout mouse; intron retention
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Year: 2019 PMID: 30638744 PMCID: PMC6649687 DOI: 10.1016/j.neuron.2018.12.019
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173