Abstract
Splicing is a crucial regulatory node of gene expression that has been leveraged to expand the proteome from a limited number of genes. Indeed, the vast increase in intron number that accompanied vertebrate emergence might have aided the evolution of developmental and organismal complexity. Here, we review how animal models for core spliceosome components have provided insights into the role of splicing in vertebrate development, with a specific focus on neuronal, neural crest and skeletal development. To this end, we also discuss relevant spliceosomopathies, which are developmental disorders linked to mutations in spliceosome subunits. Finally, we discuss potential mechanisms that could underlie the tissue-specific phenotypes often observed upon spliceosome inhibition and identify gaps in our knowledge that, we hope, will inspire further research.
Originalsprog | Engelsk |
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Artikelnummer | dev200373 |
Tidsskrift | Development |
Vol/bind | 149 |
Udgave nummer | 19 |
ISSN | 0950-1991 |
DOI | |
Status | Udgivet - 2022 |
Bibliografisk note
Funding Information:We thank current and former members of the Kanadia lab for helpful discussions and comments on the manuscript. The authors’ research is funded by the National Institute of Neurological Disorders and Stroke (R01NS102538). Deposited in PMC for release after 12 months.
Funding Information:
The authors’ research is funded by the National Institute of Neurological Disorders and Stroke (R01NS102538). Deposited in PMC for release after 12 months.
Publisher Copyright:
© 2022. Published by The Company of Biologists Ltd.