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Exon junction complex dependent mRNA localization is linked to centrosome organization during ciliogenesis
OS. Kwon, R. Mishra, A. Safieddine, E. Coleno, Q. Alasseur, M. Faucourt, I. Barbosa, E. Bertrand, N. Spassky, H. Le Hir
Language English Country Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
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- MeSH
- Autoantigens metabolism MeSH
- Cell Cycle MeSH
- Centrosome metabolism MeSH
- Cilia metabolism MeSH
- Cytoskeletal Proteins metabolism MeSH
- DEAD-box RNA Helicases metabolism MeSH
- Eukaryotic Initiation Factor-4A metabolism MeSH
- Exons genetics MeSH
- Nuclear Proteins metabolism MeSH
- Humans MeSH
- RNA, Messenger metabolism MeSH
- Microtubules metabolism MeSH
- Mice MeSH
- Neural Stem Cells metabolism MeSH
- Cell Proliferation MeSH
- Microtubule-Associated Proteins metabolism MeSH
- Cell Cycle Proteins metabolism MeSH
- RNA-Binding Proteins metabolism MeSH
- Protein Biosynthesis MeSH
- RNA Transport * MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Exon junction complexes (EJCs) mark untranslated spliced mRNAs and are crucial for the mRNA lifecycle. An imbalance in EJC dosage alters mouse neural stem cell (mNSC) division and is linked to human neurodevelopmental disorders. In quiescent mNSC and immortalized human retinal pigment epithelial (RPE1) cells, centrioles form a basal body for ciliogenesis. Here, we report that EJCs accumulate at basal bodies of mNSC or RPE1 cells and decline when these cells differentiate or resume growth. A high-throughput smFISH screen identifies two transcripts accumulating at centrosomes in quiescent cells, NIN and BICD2. In contrast to BICD2, the localization of NIN transcripts is EJC-dependent. NIN mRNA encodes a core component of centrosomes required for microtubule nucleation and anchoring. We find that EJC down-regulation impairs both pericentriolar material organization and ciliogenesis. An EJC-dependent mRNA trafficking towards centrosome and basal bodies might contribute to proper mNSC division and brain development.
Equipe labélisée Ligue Nationale Contre le Cancer University of Montpellier CNRS Montpellier France
Institut de Génétique Moléculaire de Montpellier University of Montpellier CNRS Montpellier France
Institute of Parasitology Biology Centre Czech Academy of Sciences Ceske Budejovice Czech Republic
References provided by Crossref.org
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